- Research article
- Open Access
Phylogeny of teleost connexins reveals highly inconsistent intra- and interspecies use of nomenclature and misassemblies in recent teleost chromosome assemblies
BMC Genomics volume 21, Article number: 223 (2020)
Based on an initial collecting of database sequences from the gap junction protein gene family (also called connexin genes) in a few teleosts, the naming of these sequences appeared variable. The reasons could be (i) that the structure in this family is variable across teleosts, or (ii) unfortunate naming. Rather clear rules for the naming of genes in fish and mammals have been outlined by nomenclature committees, including the naming of orthologous and ohnologous genes. We therefore analyzed the connexin gene family in teleosts in more detail. We covered the range of divergence times in teleosts (eel, Atlantic herring, zebrafish, Atlantic cod, three-spined stickleback, Japanese pufferfish and spotted pufferfish; listed from early divergence to late divergence).
The gene family pattern of connexin genes is similar across the analyzed teleosts. However, (i) several nomenclature systems are used, (ii) specific orthologous groups contain genes that are named differently in different species, (iii) several distinct genes have the same name in a species, and (iv) some genes have incorrect names. The latter includes a human connexin pseudogene, claimed as GJA4P, but which in reality is Cx39.2P (a delta subfamily gene often called GJD2like). We point out the ohnologous pairs of genes in teleosts, and we suggest a more consistent nomenclature following the outlined rules from the nomenclature committees. We further show that connexin sequences can indicate some errors in two high-quality chromosome assemblies that became available very recently.
Minimal consistency exists in the present practice of naming teleost connexin genes. A consistent and unified nomenclature would be an advantage for future automatic annotations and would make various types of subsequent genetic analyses easier. Additionally, roughly 5% of the connexin sequences point out misassemblies in the new high-quality chromosome assemblies from herring and cod.
Large-scale sequencing techniques developed since the turn of the century have caused a virtual explosion of species with sequenced genomes. A critical part of making all these genomes useful is the process of annotation, of which gene identification and gene naming are indispensable parts [1,2,3]. Computerized annotation by algorithms and the use of previously identified sequences available in databanks are needed to keep up with the flow of new genomes. However, computerized annotations are only as good as the assumptions behind the algorithms and the available data, including identifications, allow.
The Human Gene Nomenclature Committee states as the first point in its summary guidelines that “each approved gene symbol must be unique” . Some general principles of naming genes in zebrafish (and by extension in other teleosts) are outlined by the Zebrafish Information Network . The Zebrafish Nomenclature Conventions states that “genes should be named after the mammalian ortholog whenever possible” . We here understand orthologs in the same meaning as originally defined by Fitch [6, 7], who divided homologs into two main classes: orthologs and paralogs. In simple terms, orthologs are the same genes in different species. All the other genes in a gene family are paralogs, whether intraspecies or interspecies. Note that in this context, the functional relationship or expression pattern is irrelevant (in contrast to some deviant definitions of orthologs, for example on p. 726 in ref. ). Thus, a pseudogene in one species can be an ortholog of a functional gene in another species, even if the pseudogene has no known function or is not expressed.
Giving unique names to unique genes  and naming teleost genes according to the mammalian ortholog  appear as sound principles. The Zebrafish Nomenclature Conventions details that in the case of duplicated genes resulting from genome duplication, “symbols for the two zebrafish genes should be the same as the approved symbol of the human or mouse ortholog followed by “a” or “b” to indicate that they are duplicated copies” . In the case of tandem gene duplication, the duplicates “with a single mammalian ortholog should have gene symbols appended with a .1, .2, using the same symbol as the mammalian ortholog” . This may not always be easy to establish unequivocally, as it requires much work and there may be a long time between the initial genome assembly and the complete genome being assembled into chromosomes. A good indication of orthology may come from phylogenetic analyses.
Of course, reality is often not simple, as both genome duplications, tandem gene duplications, gene losses, the formation of pseudogenes, retrotranscription and reinsertion, and other genetic events may have occurred since the evolutionary separation of the different species in question. Two genome duplications occurred during the early evolution of vertebrates after the divergence of the urochordates [9,10,11]. These genome duplications are common to both teleosts and tetrapods. Additionally, another genome duplication occurred in the early evolution of teleosts [12,13,14].
The pairs of genes created by genome duplication are called ohnologs [15, 16]. As such, ohnologs are a specific subgroup of paralogs [6, 7]. Being on different chromosomes, different genetic events may happen for each member of an ohnologous pair, such as mutations of various kinds, gene losses, tandem gene duplication at one of the sites, etc. It is therefore not necessarily a 1:1 relationship between ohnologs in teleosts (e.g., one of the ohnologs could be lost in one or several species), or between mammalian and teleost orthologs [6, 7]. Furthermore, the synteny (the linear order of genetic elements in DNA) can be muddled. Adding to this evolutionary genetic complexity, there are also technical and bioinformatic caveats, making complete and perfect genome assemblies unlikely. Presently, the published genome assemblies are often estimated to be around 90% complete [17, 18], being in thousands of scaffolds instead of a few tens of chromosomes. Moreover, numerous kinds of assembly errors [19, 20] can further complicate the annotation process.
It was early observed that certain gene families had unusually large number of members in fish model species . One of these gene families is the gap junction protein gene family, encoding the proteins called connexins (for simplicity, we will generally refer to the genes as connexin genes). This family has approximately twice as many members in teleost species as in other vertebrates [22,23,24], and as such has retained more than its fair share of genes generated by genome duplication compared with many other gene families, which generally retain 1 to 20% of the duplicated genes (see review by Glasauer and Neuhauss ).
Both a size-based (in kiloDalton) nomenclature and a Greek nomenclature have been used in naming the genes in this family (e.g., connexin43, abbreviated cx43, in the size nomenclature is the same as gap junction protein alpha 1 gene, abbreviated gja1, in the Greek nomenclature). A disadvantage with a size-based nomenclature is that the protein size may vary in different species, and thus the relationship with the corresponding genes/proteins in other species may not be immediately clear. The Greek nomenclature divides the group into the subfamilies alpha (gja), beta (gjb), gamma (gjc), delta (gjd) and epsilon (gje) and with a number that initially stated the chronology of gene detection. The Human and Mouse Gene Nomenclature Committees have decided to use the Greek gene nomenclature for the connexin genes. A novel connexin nomenclature was very recently suggested by Premzl , but only mammals were taken into consideration.
The connexin genes are chordate-specific genes, urochordates being the most primitive organisms having these genes [24, 27], which in the vertebrates have evolved into the distinct subfamilies [22, 24, 28, 29]. The connexin proteins are transmembrane molecules that aggregate into hexamers forming a pore through the membrane, often called a hemichannel. Traditionally, it was supposed that hemichannels would not act alone, but rather line up with a corresponding hemichannel from the neighboring cell to form a channel directly from the cytosol in one cell to the cytosol in the other cell, through which small water-soluble molecules and ions can diffuse . In some tissues, such as the heart and uterus, these channels are of utmost importance for passing the electrical impulse from cell to cell, making these organs contract in a synchronized manner [31, 32]. The channels are probably also involved in cellular homeostasis and growth control , possibly through interactions with numerous proteins involved in signaling and regulation [34,35,36]. Additionally, there are now strong indications that hemichannels are functional in their own right [37,38,39].
The teleosts are the most species-rich group among vertebrates. In connection with the sequencing and assembly of the Atlantic herring genome , we collected some teleost connexin sequences, and soon noticed that the naming appeared variable. The two most obvious explanations for the variability were (i) that the structure in this family is variable across the teleosts, or (ii) unfortunate naming. We therefore examined the connexins in teleost species more closely, and selected species spanning the range of divergence times in this vertebrate group [41, 42]. A genome duplication occurred at the basis of the teleosts ~ 350 million years ago, and the Elopomorpha (to which eels belong) was the first group to diverge ~ 300 million years ago, and hence we selected Japanese eel (Anguilla japonica), partly supported by European and American eel (Anguilla anguilla and Anguilla rostrata) [43,44,45,46]. The Clupeiformes, to which Atlantic herring (Clupea harengus) [17, 40] belongs, and Cypriniformes, to which zebrafish (Danio rerio)  belongs, had a common divergence ~ 250 million years ago, and soon after (~ 240 million years ago) split into separate groups. The Acantomorphata diverged ~ 150 million years ago, and later split into several subgroups, of which the Gadiformes, to which Atlantic cod (Gadus morhua)  belongs, is one. The Perciformes, to which three-spined stickleback (Gasterosteus aculeatus)  belongs, diverged ~ 100 million years ago. The Tetraodontiformes (pufferfishes) are among the most recently diverged groups, ~ 70 million years ago, and both Japanese pufferfish (Takifugu rubripes, often called Fugu rubripes, and here called Fugu) and green spotted pufferfish (Tetraodon nigroviridis, here called Tetraodon) are members of this group. The two pufferfishes have very condensed genomes compared with most other teleosts [50, 51].
As the genes should be named after the mammalian ortholog whenever possible , the connexin sequences from several mammals were included. The sequences were analyzed phylogenetically, using the names indicated in the databases whenever possible. Our results show that a considerable degree of inconsistency exists in the naming of the connexin genes in fish species. There is even a case of inconsistent naming among the human sequences. In our opinion, making the naming in this gene family more congruent and consistent is indeed possible, which will improve the quality and usefulness of future genome annotations.
The structure of the teleost gap junction protein gene family
The compressed tree with the connexin subfamilies for teleosts and mammals is shown in Fig. 1. All sequences involved are shown in Suppl. Fig. 1–12. A few of the expanded branches are shown in Figs. 2-6 (Fig. 2, gjb7; Fig. 3, gja4; Fig. 4, gjd2; Fig. 5, the “gjb4like” complex; Fig. 6, cx39.2), and the remaining branches are shown in Suppl. Fig. 14.Footnote 1 In this tree, and in all trees made for the major statistical analyses (Suppl. Table 1), the GJE1/gje1/cx23 group was omitted, because the inclusion of the GJE1 orthologous group caused long-branch attraction [53, 54]. In fact, the long-branch attraction was so intense that it ripped apart both the delta and gamma subfamilies, and caused the highly variable groups of GJC3 and GJD4 to locate in the vicinity of the GJE1 group (compare Fig. 1 and Suppl. Fig. 15). However, we did include a human pseudogene in the Cx39.2 group (Fig. 6), but not the corresponding pseudogenes from some other mammals (Suppl. Fig. 12). This orthologous group is further discussed below. We also excluded rodent gja6 (which is the ortholog of the human pseudogene sometimes called Cx43pX ) and a cod gjd2 sequence (Gm-NN-gjd2*1-G01582). This sequence often split out from its expected gjd2 group, and we excluded it to make clearer distinctions within the different gjd2 groups.
Overall, it was evident that the structure of the connexin gene family was similar across all the teleosts. There were examples of species-specific gene duplications or lack of genes, but at the present time we cannot with certainty ascribe all such “anomalies” to biological and genetic reality or to partial genome sequencing and/or erroneous genome assembly. The overall similarity should make it rather simple to extend the gene identifications to other teleost species when their genomes are sequenced, thereby easing their annotation. However, this is dependent on consistency in naming of the genes in the family, which is presently at lack as shown below.
The mixture of nomenclatures
As can be seen in Figs. 2 to 6 (and also in Suppl. Fig. 14 and Suppl. Tables 3–6), there was often little consistency in naming within many of the gene clades, as some of the genes were named by the size nomenclature and others are named by the Greek nomenclature. We will here sum up the nomenclature for some of the teleost species. More details are found in the Supplementary Tables and Supplementary Figures.
Zebrafish is undoubtedly the most highly investigated teleost , with its genome sequencing starting in 2001, the first genome assemblies available in Ensembl around 2005, with the latest assemblies and annotations from 2017/2018 (Ensembl release 91, CRCz11). Thus, we would expect the gene nomenclature to be of good standard and being consistent with the intentions expressed in the Zebrafish Nomenclature Conventions . In zebrafish, among the 38 unique and predicted genes present in GenBank (Suppl. Table 3 and Suppl. Fig. 5), 25 genes followed the size nomenclature and 13 genes followed the Greek nomenclature. The naming of 37 predicted genes in Ensembl was rather similar to GenBank, with 31 sequences having the same name as in Ensembl (Suppl. Table 3).
Fugu was the first teleost with its genome published , with the last genome assembly from 2011 (in Ensembl) and annotations from 2018 . In July 2019, the Fugu annotation was updated in GenBank. Many of the previous GenBank predictions changed names from the combined Greek and size nomenclature (gja1-cx43) to Greek nomenclature only (gja1). In many cases the accession numbers also changed (Suppl. Table 4). After the GenBank update, three genes followed the size nomenclature and 38 genes followed Greek nomenclature. One previously predicted gene (Fr-gja3like-XM_003970457) was lost in the update. Fourteen genes can now be said to have the same naming in GenBank and Ensembl (disregarding upper/lower case letters, and considering gja5a = gja5), all in the Greek nomenclature (Suppl. Table 4). In Ensembl, 16 Fugu genes followed the Greek nomenclature, 21 genes followed size nomenclature, one gene had no name, and four genes were not predicted (Suppl. Table 4).
For cod sequences in Ensembl (Suppl. Fig. 10, Suppl. Table 5), eight followed Greek nomenclature (six in upper case and two in lower case), 18 followed size nomenclature, 17 were predicted but not named, and one was not predicted (but found by us). The recently available cod chromosome level genome assembly in GenBank  and the corresponding gene predictions provided us with the possibility to compare the naming of the new GenBank predictions with the Ensembl cod gene predictions (Suppl. Table 5). Only four sequences had been given the same name in Ensembl and GenBank (considering lower/upper case letters as identical; Suppl. Tables 4 and 6).
For the GenBank predictions in herring, 32 genes followed the Greek nomenclature, four followed the size nomenclature, and eight followed a mixed nomenclature, in addition to two non-predicted genes (one of them, gja8, considered as a part of an unrelated gene; Suppl. Fig. 9 and Suppl. Table 6). In the recent annotation from the novel chromosomal level assembly of herring added to the Ensembl database (Sept. 2019) , the predictions contained nine genes in Greek nomenclature and 20 genes in size nomenclature, in addition to 14 predicted genes with no name, and three genes that were lost, probably due to erroneous genome assembly (see below) (Suppl. Table 6). Only two genes had completely identical names in Ensembl and GenBank; four genes if upper/lower case letters and combination Greek-size nomenclatures were considered identical to the lower case Greek nomenclature.
Only a few of the eel connexins in the GenBank transcriptome shotgun assemblies had been named, with several having a hybrid nomenclature not commonly used (such as CXA5, cxb1, CXG1, etc.).
Multiple names for a distinct ortholog within teleosts
There were three common inconsistencies within an orthologous group, two of which are considered in this section, and the third in the next section. The first was that some genes within the group are named according to the Greek nomenclature, and other genes according to the size nomenclature. For example, within the GJB7 group (also called connexin25 in mammals), some teleost sequences were named gjb7 and other sequences were named cx28.8, and some combined the Greek and size nomenclature such as gjb7-cx25 (Fig. 2).
The second inconsistency was that evident orthologs had been given different numbers in the Greek nomenclature. One example was the teleost orthologs for mammalian GJA4, also called connexin37 (Fig. 3). They were called gja4 in Fugu, cx39.4 in Tetraodon, stickleback and zebrafish, and gja6like in Atlantic herring. It should be noted that GJA6 is a different gene group that was generated by a mammalian-specific gene duplication of GJA1 (connexin43), maybe by retrotransposition. GJA6 is a pseudogene in humans and some other species (called connexin43-related pseudogene on the X chromosome, Cx43pX, in ref. [23, 29]). In other species, including rodents, dog and elephant, GJA6 appears to be a functional gene [23, 29]. Another example is found within the major GJD2 group (Fig. 2c). Zebrafish NM_001128766 and stickleback ENSGACG00000020357 (no GenBank entry) were both called gjd1a, whereas the orthologs in Fugu were both called gjd2like (Fig. 4).
Distinct genes having identical names
The third common inconsistency was that clearly different sequences had the same name. In Fugu (using the GenBank sequences predicted before July 2019), there were two of each for Cx32.2like, gjb1like, gjb2like, and gjb3like genes; three gja3like and gjc1like genes; and four gjb4like and gjd2like genes (Fig. 4; Suppl. Table 4 and 7).
Atlantic herring (Clupea harengus) had its genome sequenced, assembled and annotated in GenBank in 2015 [17, 58], and a recently a chromosomal level assembly [59, 60] was annotated in Ensembl in the fall of 2019 . Thus, the prediction and naming of the genes should describe much of the current status for automatic annotation. In the GenBank 2015 annotation, there were two of each for gja5like, gjd2, and gjd3like; three of Cx32.2, gjc1like and gjd2like genes; and four genes called gja3like and gjb4like (Fig. 4, Suppl. Table 6 and 7). In the Ensembl annotation, each of the names occurred only once, but on the other hand, 14 of the gene predictions were un-named (Suppl. Table 6).
We will use teleost gjd2like and gjd2 as examples. Gjd2like was used in several more or less closely related genes in the delta subfamily. More specifically, sequences with this name were found among the cx36.7, cx39.2, and the central gjd2 groups. These groups are shortly discussed below.
The central gjd2 group (Fig. 4) is a complex of sequences that are all closely related to the mammalian GJD2. Previously, these genes were named connexin36 in mammals and connexin35 or connexin35.1  in fish. While mammals have one GJD2 gene, teleosts have up to four (as in zebrafish, Fugu, and stickleback) in this central gjd2 group. For convenience, we named groups of the teleost genes in the central gjd2 group as gjd2*1, gjd2*2 and gjd2*3, because they sometimes split into three groups, depending on the statistical analysis. Occasionally, one or two sequences split out of the gjd2*1 group, and ended in-between the other gjd2/GJD2 groups. This happened particularly often with Gm-NN-gjd2*1-G01582 (sequence found in Suppl. Fig. 10), which is why we excluded this sequence during the statistical analyses. Generally, the sequences within gjd2*2 and gjd2*3 stayed as unified groups, usually as a dichotomous clade (for discussion of ohnologies within these groups, see below).
The mammalian GJD2 is somewhat promiscuous in terms of which teleost sequence group it most closely adhered to, but most often it was gjd2*1 or gjd2*2. In zebrafish, these genes are among the few places where “a” and “b” have been added to some of the gene names in the databases. In the gjd2*2/*3 group, one of the zebrafish (and stickleback) genes is called gjd1a (but there is no gjd1b) and the other gjd2like. In the gjd2*1 group, one of ohnologs in zebrafish, Tetraodon, stickleback and cod is called gjd2b (but there is no gjd2a).
Another group named gjd2like (in Fugu and Atlantic herring) was the cx36.7 group, called Dr17927 in a previous paper . This group often branched off from the foot of the central gjd2 complex itself (Fig. 1), but in a few statistical analyses it located closer to gjd3 or gjd4 (Suppl. Table 1). As yet, there are no mammalian members in this group, and our previous work  suggested that this group was specific to fish.
Another orthologous group often named gjd2like has previously, and more uniquely, been called cx39.2 . This orthologous group divided its location between the delta (most commonly) and gamma subfamilies depending on the model run, but it never located within or at the foot of the central gjd2 group (in contrast to cx36.7). The first mammalian member in the cx39.2 group was found in opossum , but we here show that this ortholog is also present in several other mammals, like several Afrotheria (Suppl. Fig. 12) and bats (Fig. 6), sometimes as obvious pseudogenes. A human pseudogene (NG_026166), named “Homo sapiens gap junction alpha 4 pseudogene on chromosome 17” (GJA4P) is not a pseudogene related to GJA4 but rather to the cx39.2 (GJD2-like) group according to the phylogenetic analyses (Fig. 6). Alignments of NG_026166 against GJA4 and representatives from the cx39.2-like group clearly indicated a closer relationship with the latter (Table 1; Suppl. Figs. 13A and 13B; Suppl. Tables 8 and 9). In a comparison at amino acid level between the conserved domains of human GJA4P and GJA4 vs. eel cx39.2 and cx39.4 (Table 1), the identity levels between the GJA4/cx39.4 (human/eel) orthologs were ~ 55%, the same as for GJA4P/cx39.2 (human/eel), which is clearly higher than GJA4P/GJA4 (human/human; ~ 38%) and GJA4P/cx39.4 (human/eel; ~ 34%). Also at nucleotide level, the human GJA4P showed higher identities to cx39.2 than to GJA4 from opossum and bat (Suppl. Table 9), e.g., conserved domains of Hs-GJA4P was 53.9% identical to opossum GJA4-XM_007492764 and 65.3% identical to opossum cx39.2 (= Md-GJD2like-XM_001376506) (Suppl. Table 9). Thus, the alignments were consistent with the phylogenetic results (Figs. 1 and 6), and thereby settled this pseudogene (NG_026166) to be incorrectly named in humans. It is not GJA4P, but rather Cx39.2P.
On teleost connexin ohnologies
The phylogenetic analyses provided a strong indication of the presence of several ohnologous pairs in teleosts. However, distinguishing between paralogous pairs that have been created by tandem gene duplication and ohnologous pairs created by genome duplication might be difficult, especially if the assembly only exists as contigs or relatively short scaffolds. If a novel teleost genome assembly is being made, it would be valuable to have the answer to this question established in other species, simply because the naming should be different in the two cases. Thus, it is of importance to show whether the ohnologous relationship can be traced across teleosts in a reasonably systematic way. In other words, is the genomic location of a gene and its potential ohnolog in one or two species sufficient to give indications for other species?
As of today, most eukaryotic draft genome assemblies consist of thousands of scaffolds, and even if these scaffolds can be Mb long, they are just a fraction of the size of most eukaryotic chromosomes. For such scaffolds, only connexin genes positioned rather closely are informative. When this analysis started, chromosomal assemblies were not available for herring and cod, but both became available during the summer of 2019 [56, 59].
For looking more closely into ohnologous pairs, the Japanese eel genome assembly was used as a starting point, because eel is a member of the early diverging fishes. Table 2 summarizes the situation for the chromosomes (or linkage groups) containing the highest number of connexin genes, and Suppl. Table 10 gives the full overview. Eel linkage group (chromosome) 19 contained eight connexin genes (gja1, cx34.5, cx28.9, cx32.2, gja10, gjb7, gjd2*1, gje1). The same eight genes were found on zebrafish chromosome 20 and stickleback chromosome 18, and at least seven of them are collected at cod chromosome 21. Thus, there is a strong tendency that linked genes in eel also are linked in the other species. For some unknown evolutionary reason, this chromosome had relatively few examples of ohnologs. The ohnologous chromosome may have gone through some kind of genetic catastrophe. In fact, for the two connexins with the highest number of species showing ohnology, gja1 and gjd2*1, the ohnologs were found on an “unexpected” chromosome (7 in eel, 14 in herring and 17 in zebrafish). We use the term “unexpected” because these ohnologs deviated more from the location patterns we found for the other connexins on eel chromosome 7 (see below).
Eel chromosome 7 contained five connexin genes, in addition to the ohnologs of gja1 and gjd2*1, namely gja4, gja9, cx28.6, cx35.4 and cx34.4, and four of their ohnologs were placed at chromosome 4 (and chromosome 19 for gja1 and gjd2*1). In stickleback, all five genes were found on chromosome 10 (but chromosome 18 for gja1 and gjd2*1), and three of the ohnologs were found on chromosome 15, the fourth ohnolog (gja9) on chromosome 20, and the fifth was missing. In Tetraodon, three of the five genes (gja4, gja9, cx28.6) were found on chromosome 21, and two of these had ohnologs, gja9 on an unplaced scaffold, and cx28.6 on chromosome 10. Tetraodon chromosome 10 also contained the single copies of cx35.4 and cx34.4. In zebrafish, gja9, cx28.6, cx35.4, and cx34.4 were found on chromosome 17. Gja4 was present as a single paralog on chromosome 19, which also contained the ohnolog of cx28.6. Thus, we see for gja4, gja9, cx28.6, cx35.4 and cx34.4 on eel chromosome 7 that there was a strong tendency towards a pattern of consistency in distribution of ohnologous pairs to distinct chromosomes in all the investigated species, while gja1 and gjd2*1 tended to deviate.
In general, teleosts had four genes that were very closely related to mammalian GJD2. Although one or two of the sequences in the gjd2*1 group occasionally split out from the remaining genes, the two ohnologs (Table 2) generally stayed together, and there should be no doubt about the proper ohnology. In 14 of 21 statistical analyses gjd2*1 grouped together with mammalian GJD2, and these were considered as the appropriate orthologs. Gjd2*2 and gjd2*3 often dichotomously grouped together (in 11 of 21 statistical analyses), but other times split up. We believe that gjd2*2 and gjd2*3 most likely are ohnologs, although it could not totally excluded that they are non-ohnologous paralogs located on different chromosomes.
If the genes that were linked in eel had broken linkages in other species, in many cases two or three of the most closely linked genes have moved to another chromosome than the rest of the group. A more complete overview containing all connexin genes and associated chromosomes is provided in Suppl. Table 10.
Of course, this analysis also showed closely related genes that were not ohnologs. E.g., the genes within the cx34.5 and cx32.2 groups (also known as cx32.7, cx32.3 and cx28.9) are not ohnologs, because they all are located on the same chromosome (19 in eel, 15 in herring, 20 in zebrafish, 21 in cod, 18 in stickleback, 14 in spotted pufferfish, and scaffold1917 in Fugu).
In summary, over the range of divergence time, large stretches of the chromosomes have been maintained reasonably intact subsequent to the teleost genome duplication. Thus, the corresponding ohnologs are found on other non-random chromosomes. However, both gene losses and tandem duplications might have occurred over the considered evolutionary period, which could complicate the interpretations. Of course, this is even further complicated by the facts that the sequencing itself is probably not able to reach a complete coverage of the genome causing the partial or full absence of a gene, and that the assembly process is not straight-forward.
Lack of expected connexin genes may point to chromosomal misassemblies
As an example of practical use of this kind of information, we here briefly apply the knowledge of the outlined patterns of the connexin genes on (i) the first published herring genome assembly [17, 62], which was used as basis for GenBank gene predictions from 2015 (XM accession numbers in GenBank); (ii) the new herring chromosome level assembly [59, 60]; and (iii) a herring genome assembly made by the present authors [40, 58]. Although the GenBank herring gene predictions were superior when compared with most other fishes (in the sense that the predictions tended to follow the expected gene patterns), there were still some features worth noting.
First, there was one easily found connexin (cx39.2) that was not predicted in the annotation from the 2015 herring genome assembly .
Second, several connexin genes showed identical or near identical duplicates in the first herring genome assembly. The gjb3like-XM_ XM012822385 (one of the ohnologs in the cx35.4 group) was identical to XM_012822374 and XM_012822365, found at three locations on scaffold NW_012217989. The gjb3like-XM_012818491 (the second ohnolog in the cx35.4 group) was identical to XM_012818489; found at two locations on scaffold NM_012210726. The gjb4like-XM_012818492 (one of the ohnologs in the cx34.4 group) was nearly identical to XM_012819490, and both were found on scaffold NW_012219726. The gjd3like-XM_012837668 was nearly identical to XM_012837669, and both were found on scaffold NW_012223269. Although such copies are not entirely biologically implausible, they are not probable, and are more likely caused by assembly errors. Indeed, in the initial states of our own assembly most of them were not present in duplicate sequences, only becoming so in the last step where our assembly was fused with the published herring genome . In the recently released (summer 2019) herring chromosome level assembly [59, 60] most of these duplicates have collapsed into a single copy of the sequence.
Third, three connexin genes have “disappeared” from the new herring chromosome level assembly. These are gja9like-XM_012824682, gjb1like-XM_012819602 and gjb7like-XM_012823856. The corresponding orthologs are found in the other teleost species, and - even more importantly - hits were found in the two other herring genome assemblies. We have verified the presence of these genes in our early assemblies . This strongly indicates misassemblies in the new chromosome level assembly. More specifically, the lack of gjb7 indicates a misassembly on chromosome 14 or 15. Indeed, an alignment of the relevant scaffold and chromosome showed breaks and inversion around the expected position of gjb7 at chromosome 15 (Fig. 7). The apparent lack of the gjb1 ohnolog indicates a misassembly on chromosome 8, where we indeed found breaks and inversions (not shown). We expected that the lack of the gja9 ohnolog to indicate a misassembly on chromosome 14, but we found the relevant scaffold to align with chromosome 11, where again breaks and inversions were found (not shown).
Regarding the third point above, also the recent chromosome level assembly in cod  showed a “no hit” for the Gm-gja10 ohnolog Gm-cx52.6-G05425 and for Gm-gja5-G04028 (Suppl. Table 5 and 10). The lack of gja5 suggested a problem in the assembly of cod chromosome 20 around position 1,000,000 (Suppl. Fig. 16A). Gm-cx52.6 is located on a small and unplaced contig (not even containing the full-length sequence of the gene), which was unusable for dot plot alignment at a chromosomal scale. By using suitable scaffolds containing the cx52.6 ortholog from herring and stickleback, we believe there is a problem in assembly of cod chromosome 21 around position 2,700,000 (Suppl. Fig. 16B and C). Other alignments using the corresponding zebrafish sequence also pointed to the same location.
A more consistent nomenclature suggestion
We believe that improved gene predictions and annotations are possible through the proper incorporation of knowledge into the algorithms. Furthermore, it would certainly help if the genes were labeled with unique names, as is one of the underlying logics in the instructions from the Human Gene Nomenclature Committee and the Zebrafish Gene Nomenclature Conventions. For most of the genes in the teleost connexin family, it is easy to suggest names that follow the nomenclature guidelines. Suppl. Fig. 17 presents a suggestion that follows the recommendations from the Human and Mouse Gene Nomenclature Committees and the Zebrafish Nomenclature Conventions, and Table 3 shows a translation between the nomenclature systems, including the recently suggested “alphabetic” system in mammals . In our suggestion, we maintain the Greek nomenclature naming and numbering of those genes that are well established names in human and mouse, and transfer the naming conventions to the corresponding orthologs in teleosts. We fully avoided the “-like” names, as they often are used for several distinct genes and thus do not indicate a concrete orthologous group, and in this way can be misleading.
The subfamily number (gjd1/2/3/4, etc.) for the groups where new names are suggested does not consider the chronological order of detection, but rather the numbers that are available. For example, cx39.9 is closely related to gja3, and is in fact often called gja3like. As gja1, gja3, gja4, gja5, and gja6 already are occupied, while gja2 is not, we suggest calling cx39.9/gja3like for gja2. The genes in the cx34.5, cx28.9 and cx32.2 groups are called gja11, gja12 and gja13, respectively. We skip gja7, as this name has historically been used for Cx45 (= GJC1).
Statistically, a strong link exists between cx35.4/gjb3like and GJB3. We therefore suggest that cx35.4 should be called gjb3, despite the lack of the hallmark of the mammalian GJB3 protein, namely the amino acid sequence CX5CX5C in the second extracellular loop, where all other connexins (except the GJE1 proteins) have the sequence CX4CX5C.
There is a particular problem in the beta subfamily in that the mammalian GJB2 and GJB6 are always located in a dichotomous manner in the phylogenetic analyses, and similarly for GJB4 and GJB5. There were no indications that cx30.3 located closer to either of GJB2 or GJB6, and similarly, cx34.4 did not locate closer to either of GJB4 or GJB5. It might be that cx30.3 is a precursor gene for both GJB2 and GJB6, and cx34.4 is a precursor gene for GJB4 and GJB5, as we have suggested earlier [23, 24]. Thus, several possibilities exist for naming these genes. Cx30.3 could be called gjb8 (following the present pattern in the Greek nomenclature), pre-gjb2/6 (indicating the potential of being a precursor for the two mammalian genes), or gjb26 (a variant of the previous, but with the potential danger that this could be mistaken for cx26). We suggest cx30.3 is called gjb8 and cx34.4 is called gjb10. We further suggest that cx28.6, which generally located at the root of ((GJB4-GJB5)-gjb10)-(GJB3-gjb3) (parentheses indicate branching structure), is called gjb9.
In the gamma subfamily, there are two groups concerned with renaming. The first one is in marsupials, where the majority of statistical analyses (Suppl. Table 1) support GJC1like/GJC2like genes probably being the orthologs of eutherian GJC3, as originally suggested . The second group is cx43.4/44.2/gjc1like, which we suggest is renamed gjc4.
In the delta subfamily, the major problems concern the gjd2 complex. As briefly discussed above, we consider gjd2*2 and gjd2*3 probable ohnologs, and suggest that they are named gjd1, fitting with a zebrafish and a stickleback sequence within this group already named gjd1. The ohnolog pairs within gjd2*1 are probably orthologs with mammalian GJD2, and consequently we suggest they are named gjd2. The teleost cx36.7/gjd2like group never dichotomized with any of the mammalian genes and most often branched off from the root of the gjd2 complex. We suggest this group should be called gjd6. The last group is the little-studied cx39.2 group, which in mammals has a variety of names in database gene predictions, such as GJC2like, GJD2like and GJA4like. The mammalian genes robustly dichotomize with the corresponding teleost genes, which in the databases usually are called gjd2like. We suggest that this clade is called GJD5 in mammals (thus, the human pseudogene NG_026166 should be called GJD5P) and gjd5 in teleosts.
The first phylogenetic analyses of the (nearly) complete connexin gene family across the vertebrates, from mammals to teleosts, were performed in the early genomic era [22,23,24, 29]. The analyses indicated that there was a considerable degree of conservation in this gene family, and that the subfamily structure could be recognized across the different vertebrate groups. Using a wide basis of teleosts, from the early diverging eels to the late diverging pufferfishes, we here confirm that the substructure of the gene family in teleosts is stable and easily recognizable. On the other hand, there is a high degree of inconsistency in the naming of the teleost genes in the connexin family in two major genetic databases, GenBank and Ensembl, both internally within each database and between the databases. The naming does not generally follow the recommended guidelines from the Human Gene Nomenclature Committee  and the Zebrafish Nomenclature Conventions . Even the annotations of the novel chromosome level genome assemblies in herring [59, 60] and cod , made available during 2019, possess such inconsistencies. A part of the differences probably reflects different annotation pipelines and the use of different databases as knowledge basis in Ensembl and GenBank.
We are confident that our overall results are robust, due to a high degree of consistency across several applied methods and parameters. We therefore suggest an amended and extended Greek nomenclature that follows the guidelines of the Human Gene Nomenclature Committee  and the Zebrafish Nomenclature Conventions . The suggestion also includes the naming for ohnologs, i.e., duplicated genes generated by genome duplication.
We noted previously that connexin genes could indicate errors in a genome assembly , like duplicated areas or areas not sequenced. Having confirmed the stability of the substructure in the gene family in teleosts, we can be even more certain that different anomalies that may come up when analyzing the complete gene family in a teleost species are pointing out potential assembly errors. These types of analyses share some common grounds with Core Eukaryotic Gene Mapping Approach (CEGMA)  and Benchmarking Universal Single Copy Orthologs (BUSCO) [64, 65], in that selected genes are investigated for their presence in a genome to verify the completeness of a newly assembled genome. They differ in that the connexins are a family of genes, consisting of several subfamilies, as well as that these genes have two conserved domains that have some reciprocal similarities.
In the context of genome assembly and gene annotation, the connexins are a randomly selected gene family. It is curious how, even in very recent high-quality genome assemblies, such as those of Atlantic herring and cod, these genes can indicate certain potential misassemblies. This situation can possibly be extended to other gene families and single genes, as the number of missing BUSCOs in the herring genome in the herring genome increased from 2.9% (131/4584) in the draft herring genome assembly  to 8.1% (374/4584) in the chromosome level assembly  according to our analysis .
It is possible to analyze an un-annotated genome for a specific genes or gene families when it is known exactly what to look for, but the value of a genome assembly increases considerably if it is well annotated. Poor annotations may mislead, and certainly may make different kinds of comparisons more difficult. For example, a synteny analysis could potentially give wrong conclusions if the gene names do not indicate the proper genetic relationships. Our results suggest that it should be fully possible to improve the annotation of the connexin gene family. We would be surprised if the inconsistencies pointed out here only concern the connexin gene family.
The practice of naming connexin genes in teleosts exhibits many inconsistencies. Commonly, distinct genes are assigned the same name, and there are examples of clearly incorrect names, even in mammals, including that of a human pseudogene (NG_026166). By using many different phylogenetic models, we could classify the teleost sequences that had a dichotomous relationship with the corresponding mammalian sequences, and thereby point out the sequences that should have the same name as their mammalian orthologous counterpart. Conversely, if there was no mammalian counterpart they should have a unique name. It was further settled which of the teleost sequences that existed in ohnologous pairs, and thereby should have their names followed by “a” or “b”. To quite some extent, it is possible to predict at which chromosome a teleost connexin should be located. We investigated two very recent high-quality chromosome assemblies (herring and cod), finding that roughly 5% of the expected connexin sequences were absent (two in cod and three in herring). We found likely misassemblies or gaps at the expected positions for the missing connexins in the chromosome assemblies.
Collection of sequences
The major procedures are schematically outlined in Suppl. Fig. 18. The collecting of sequences was done by several approaches. First, previously collected sequences [23, 24, 29] were checked against the present and updated versions of the genomes to include potential revisions of the gene sequences. This was done by searching GenBank (nucleotide collection, whole genome contigs, transcriptome shotgun assemblies, and specific genome assemblies), using nucleotide BLAST [66, 67], and Ensembl, using the corresponding BLAST/BLAT option built into Ensembl, in both cases obtaining pairwise alignments between our old sequences and the present sequences in the databases. Second, annotated and named sequences were found by using “connexin”, “gap junction protein”, “gja”, “gjb”, “gjc”, “gjd”, “gje” and the relevant species names as search terms in GenBank and Ensembl. If there was a lack of certain expected sequences in a certain species, the genome assemblies for the species in question were searched using the corresponding (assumed) orthologs from other species. When needed, multiple alignments by MUSCLE  were done, e.g., to settle the probable borders between introns and exons and to determine the percentages of identities between different sequences (e.g., in Suppl. Figs. 13A and 13B). By the combination of approaches described above, we found several connexin sequences presently not predicted in the databases, and they were included in our analyses (marked by NP as described below under Naming terminology).
If the experimentally confirmed or predicted sequences were available in GenBank, their accession numbers were also collected (to ensure the unique naming of the sequences). Depending on species and gene in question, we have used the NCBI Reference Sequences whenever possible. Otherwise, gene/RNA names or numbers were collected from Ensembl. All sequences, with GenBank accession numbers or Ensembl gene numbers if relevant, are provided in Supplement Figs. 1–12.
Among teleosts, we have collected sequences from zebrafish (Danio rerio, abbreviated Dr), stickleback (Gasterosteus aculeatus, Ga) , Japanese pufferfish (Takifugu rubripes, often called Fugu rubripes, called Fugu in the text, and abbreviated Fr) [50, 70], green spotted pufferfish (Tetraodon nigroviridis, Tn) , Atlantic herring (Clupea harengus, Ch) [17, 62], Atlantic cod (Gadus morhua, Gm) [48, 72] and European, American or Japanese eel (Anguilla anguilla, Aa; Anguilla rostrata, Ar; or Anguilla japonica, Aj). For eel, we have chosen to refer to an improved Anguilla japonica assembly [73, 74] because it has by far the longest scaffolds, aided by other genome shotgun assemblies of A. japonica , A. anguilla  and A. rostrata , as well as transcriptome shotgun assemblies from A. anguilla [76,77,78] and A. japonica .
As a comparison for the fish sequences, and to follow the Zebrafish Nomenclature Conventions , we collected sequences from humans (Homo sapiens, Hs; Suppl. Fig. 1), mouse (Mus musculus, Mm; Suppl. Fig. 2), and opossum (Monodelphis domestica, Md; Suppl. Fig. 3), and supplemented them with certain single sequences from platypus (Ornithorhynchus anatinus, Oa), koala (Phascolarctos cinereus), Tasmanian devil (Sarcophilus harrisii, Sh), wallaby (Notamacropus eugenii), large flying fox (Pteropus vampyrus, Pv), black flying fox (Pteropus alecto, Pa), Egyptian rousette (Rousettus aegyptiacus, Ra), aardvark (Orycteropus afer afer, Afer), manatee (Trichechus manatus, Tm), African elephant (Loxodonta africana, La) and armadillo (Dasypus novemcinctus, Dn) (Suppl. Figs. 4 and 12). All sequences are given in the Supplemental Information, where also the relevant database can be inferred according to the name/identity we have given the sequence.
Suggested deviations from the predicted sequences are indicated in the Supplemental Information. If the predicted sequences did not contain potential start and stop codons, we analyzed the genomes to extend the sequences to those codons, following the pattern established by connexins orthologs in other species. If the predicted sequences contained introns, we investigated whether moving the exon-intron borders improved the similarity between sequences and the established sequence patterns, even by including the whole intron as a part of the exon. In a few cases, we also suggested other types of modifications, following the patterns established for these sequences in other species. Furthermore, any unpredicted sequences (i.e., those not predicted in Ensembl or GenBank) we found during the present searches, were included.
Several pseudogenes exist in the gap junction gene family, also in humans . With a single exception, obvious pseudogenes are not included in the analyses shown. The one exception is a novel human pseudogene (GenBank NG_026166; claimed as GJA4 pseudogene) that we did not detect in our previous analyses [23, 24, 29]. Additionally, orthologs to NG_026166 were extracted from the genomes of several mammalian species (Suppl. Fig. 12).
To distinguish between human genes and other species, it is generally recommended that abbreviations for human gene names are spelled in upper case letters, while using lower case letters for other species. For the purpose of the present paper, this would be inconvenient as we often are referring to the gene groups, and we are here using upper case when referring to human genes and mammalian orthologous gene groups, while teleost genes in general are indicated by lower case letters. We also use upper case letters when we are referring to a whole orthologous group (i.e., mammalian plus teleost genes). There are some exceptions to the upper/lower case spelling, because when we refer to specific single genes, we use (as far as possible) the gene names given in GenBank or Ensembl.
To ensure uniqueness of every name used in the present work, we added the GenBank accession number or an abbreviated form of the Ensembl gene number to the names for which predictions were available in the present databases. Specific gene names were generally abbreviated as indicated by the database, or the abbreviations can be inferred from the database name. E.g., for XM_003965660, the full name (“definition”) is “Takifugu rubripes gap junction protein, alpha 9, 59 kDa (gja9), mRNA”. In this case, the name is given with both the Greek and size nomenclature, and the name is abbreviated in lower case in parentheses. Thus, we have here used the gene name Fr-gja9-cx59-XM_003965660. For XM_021466745, the full name is “Danio rerio connexin 55.5 (cx55.5), transcript variant X1, mRNA”. We here abbreviated the name to Dr-cx55.5-XM_021466745. For XM_011619942, the full name is “Takifugu rubripes gap junction alpha-10 protein-like (LOC1010664818), mRNA”, and it was abbreviated Fr-gja10like-XM_011619942. Where several transcript variants are experimentally shown or predicted, we only used transcript variant X1.
If the gene was predicted in the Ensembl database, but no name was available, we used a relevant gene name to indicate the correct group of sequences. For example, the Tetraodon gjb2/6-like sequence ENSTNIG00000010340 (with the corresponding transcript prediction ENSTNIT00000013438) had no name or description. We abbreviated the gene Tn-NN-cx30.3-G10340 (where NN = No Name). This is an example of a gene for which our transcript prediction differed from the database, as indicated in the Supplemental Information.
If the gene was not predicted in a species, but found in our Blast searches, it was suitably named but with the prefix NP (Not Predicted). One example is Tn-NP-cx30.3. Thus, Tetraodon has a total of four genes in the Cx30.3 group, two that have been predicted and are named in Ensembl, one that has been predicted but not named, and one that has not been predicted by the database (but by us).
To be able to follow certain very closely related groups of sequences in an easy manner, previously un-named (or unpredicted) sequences in the cx30.3 and gjd2 groups were named with the postfixes *1/*2/*3 for the purposes of the present manuscript.
The phylogenetic analyses were performed in MEGA7  or MEGA-X  using the conserved domains essentially as described in Cruciani and Mikalsen  because of the distant evolutionary relationship between mammals and fish. Here, we extended the previously defined conserved domains by 15 nucleotides in 3′-direction for the first conserved domain (i.e., into the sequence corresponding the intracellular loop), and by 15 nucleotides in both 5′- and 3′-direction for the second conserved domain. All sequences and the limits of the sequences used in the phylogenetic analyses are presented in the Suppl. Fig. 1–12, where previously defined conserved sequences  are marked in yellow, and the 15 nucleotide extensions are marked in grey.
The main questions for the phylogenetic analyses were related and also partly overlapping, and were as follows: (i) The connection between the naming of the teleost sequences (naming taken from the main databases GenBank and Ensembl) and their position in a specific orthologous group, i.e., do teleost orthologs have the same name? (ii) The (orthologous) relationships between the teleost sequences and the corresponding mammalian sequences. Is there a (reasonably) stable structure in the connexin gene family across the teleosts, i.e., do teleost connexins distribute into orthologous groups in a manner more or less similar to the mammalian sequences? (iii) The ohnologies among the teleost sequences. Note that our present questions do not concern the relatedness within the whole tree (i.e., the complete evolutionary history of the connexin gene family). The present knowledge of evolutionary history of the connexin gene family is graphically summarized in Fig. 4 in ref. . The needed translation between the nomenclature systems is found in Table 3. This translation also includes the recently suggested “alphabetical” nomenclature in mammals .
Model selection was run in MEGA X using amino acid models. Settings were automatic tree building using Neighbor-Joining model and partial deletion using a site coverage cutoff of 95%. Minimal differences were found between the models estimated with similar Bayesian Information Criterion, but in general simpler models were preferred (Jones-Taylor-Thornton, Le-Gascuel and Dayhoff substitution matrices). We therefore ran the phylogenetic analyses with different construction methods (Maximum Likelihood, Maximum Parsimony and the two distance methods Neighbor-Joining and Minimum Evolution) using different substitution models as indicated in Suppl. Table 2. Several construction methods were used as they have different strengths and weaknesses with regard to the degree of relatedness of the sequences, the differences in evolutionary rates in different branches, how highly divergent sequences are behaving, etc. Settings for each particular analysis are available in Suppl. Table 2. Each method was used at both amino acid and nucleotide levels (the latter using only positions 1 and 2 in the codon), and in many cases with both bootstrap and interior branch statistics. In total, 21 statistical analyses were performed, and they are summarized in Suppl. Table 1, with the corresponding parameter settings in Suppl. Table 2. All these methods are included in the MEGA phylogenetic software. If all, or most, of the statistical comparisons supported a specific dichotomous relationship, we deemed the results more robust.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional files. All sequences, with all required information, are in the Additional File 1. Please note that the data have been handled manually, and human error and inconsistencies may have occurred. If significant errors are detected, we would be grateful to receive a notification.
Please note that the naming of each single sequence in most of the figures and tables follows as closely as possible the naming and orthography (including lower and upper case letters) in the respective databases from where the sequences were collected (see also detailed explanation in the Methods section and in legend to Fig. 2).
Benchmarking Universal Single Copy Orthologs
Core Eukaryotic Gene Mapping Approach
Gap junction protein alpha gene
Gap junction protein beta gene
Gap junction protein gamma gene
Gap junction protein delta gene
Gap junction protein epsilon gene
Gaasterland T, Oprea M. Whole-genome analysis: annotations and updates. Curr Opin Struct Biol. 2001;11:377–81.
Stein L. Genome annotation: from sequence to biology. Nat Rev Genet. 2001;2:493–503.
Rouze P, Pavy N, Rombauts S. Genome annotation: which tools do we have for it? Curr Opin Plant Biol. 1999;2:90–5.
Human Gene Nomenclature Committee [https://www.genenames.org/about/guidelines/]. Accessed 11 Feb 2019.
Zebrafish Information Network [https://wiki.zfin.org/display/general/ZFIN+Zebrafish+Nomenclature+Conventions]. Accessed 25 Mar 2019.
Fitch WM. Distinguishing homologous from analogous proteins. Syst Zool. 1970;19:99–113.
Fitch WM. Homology. A personal view on some of the problems. Trends Genet. 2000;16:227–31.
Hartl DL, Cochrane BJ. Genetics. Analysis of genes and genomes, 9th Ed. Burlington, MA: Jones and Bartlett Learning; 2018.
Putnam NH, Butts T, Ferrier DE, Furlong RF, Hellsten U, Kawashima T, Robinson-Rechavi M, Shoguchi E, Terry A, Yu JK, et al. The amphioxus genome and the evolution of the chordate karyotype. Nature. 2008;453:1064–71.
Smith JJ, Kuraku S, Holt C, Sauka-Spengler T, Jiang N, Campbell MS, Yandell MD, Manousaki T, Meyer A, Bloom OE, et al. Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution. Nat Genet. 2013;45:415–21.
Ohno S. Evolution by gene duplication. Berlin: Springer Verlag; 1970.
Taylor JS, Braasch I, Frickey T, Meyer A, Van de Peer Y. Genome duplication, a trait shared by 22000 species of ray-finned fish. Genome Res. 2003;13:382–90.
Meyer A, Van de Peer Y. From 2R to 3R: evidence for a fish-specific genome duplication (FSGD). Bioessays. 2005;27:937–45.
Vandepoele K, De Vos W, Taylor JS, Meyer A, Van de Peer Y. Major events in the genome evolution of vertebrates: paranome age and size differ considerably between ray-finned fishes and land vertebrates. Proc Natl Acad Sci U S A. 2004;101:1638–43.
Wolfe K. Robustness--it's not where you think it is. Nat Genet. 2000;25:3–4.
Postlethwait JH. The zebrafish genome in context: ohnologs gone missing. J Exp Zool B Mol Dev Evol. 2007;308:563–77.
Martinez Barrio A, Lamichhaney S, Fan G, Rafati N, Pettersson M, Zhang H, Dainat J, Ekman D, Hoppner M, Jern P, et al. The genetic basis for ecological adaptation of the Atlantic herring revealed by genome sequencing. eLife. 2016;5:e12081.
Cai H, Li Q, Fang X, Li J, Curtis NE, Altenburger A, Shibata T, Feng M, Maeda T, Schwartz JA, et al. A draft genome assembly of the solar-powered sea slug Elysia chlorotica. Sci Data. 2019;6:190022.
Vezzi F, Narzisi G, Mishra B. Reevaluating assembly evaluations with feature response curves: GAGE and assemblathons. PLoS One. 2012;7:e52210.
Gurevich A, Saveliev V, Vyahhi N, Tesler G. QUAST: quality assessment tool for genome assemblies. Bioinformatics. 2013;29:1072–5.
Amores A, Force A, Yan YL, Joly L, Amemiya C, Fritz A, Ho RK, Langeland J, Prince V, Wang YL, et al. Zebrafish hox clusters and vertebrate genome evolution. Science. 1998;282:1711–4.
Eastman SD, Chen TH, Falk MM, Mendelson TC, Iovine MK. Phylogenetic analysis of three complete gap junction gene families reveals lineage-specific duplications and highly supported gene classes. Genomics. 2006;87:265–74.
Cruciani V, Mikalsen SO. The vertebrate connexin family. Cell Mol Life Sci. 2006;63:1125–40.
Cruciani V, Mikalsen SO. Evolutionary selection pressure and family relationships among connexin genes. Biol Chem. 2007;388:253–64.
Glasauer SMK, Neuhauss SCF. Whole-genome duplication in teleost fishes and its evolutionary consequences. Mol Gen Genomics. 2014;289:1045–60.
Premzl M. Comparative genomic analysis of eutherian connexin genes. Sci Rep. 2019;9:16938.
Sasakura Y, Shoguchi E, Takatori N, Wada S, Meinertzhagen IA, Satou Y, Satoh N. A genomewide survey of developmentally relevant genes in Ciona intestinalis. X. Genes for cell junctions and extracellular matrix. Dev Genes Evol. 2003;213:303–13.
Bennett MV, Zheng X, Sogin ML. The connexins and their family tree. Soc Gen Physiol Ser. 1994;49:223–33.
Cruciani V, Mikalsen SO. The connexin gene family in mammals. Biol Chem. 2005;386:325–32.
Harris AL. Emerging issues of connexin channels: biophysics fills the gap. Q Rev Biophys. 2001;34:325–472.
Procida K, Jorgensen L, Schmitt N, Delmar M, Taffet SM, Holstein-Rathlou NH, Nielsen MS, Braunstein TH. Phosphorylation of connexin43 on serine 306 regulates electrical coupling. Heart Rhythm. 2009;6:1632–8.
Kidder GM, Winterhager E. Physiological roles of connexins in labour and lactation. Reproduction. 2015;150:R129–36.
Mesnil M. Connexins and cancer. Biol Cell. 2002;94:493–500.
Genet N, Bhatt N, Bourdieu A, Hirschi KK. Multifaceted roles of connexin 43 in stem cell niches. Curr Stem Cell Rep. 2018;4:1–12.
Sorgen PL, Trease AJ, Spagnol G, Delmar M, Nielsen MS. Protein-protein interactions with connexin 43: regulation and function. Int J Mol Sci. 2018;19:1428.
Sundset R, Ytrehus K, Mikalsen SO. Connexin, connection, conductance: towards understanding induction of arrhythmias? Heart Rhythm. 2009;6:1639–40.
Bennett MV, Contreras JE, Bukauskas FF, Saez JC. New roles for astrocytes: gap junction hemichannels have something to communicate. Trends Neurosci. 2003;26:610–7.
Wang N, De Bock M, Decrock E, Bol M, Gadicherla A, Vinken M, Rogiers V, Bukauskas FF, Bultynck G, Leybaert L. Paracrine signaling through plasma membrane hemichannels. Biochim Biophys Acta. 1828;2013:35–50.
Orellana JA, Saez JC, Bennett MV, Berman JW, Morgello S, Eugenin EA. HIV increases the release of dickkopf-1 protein from human astrocytes by a Cx43 hemichannel-dependent mechanism. J Neurochem. 2014;128:752–63.
Kongsstovu S, Mikalsen SO, Homrum EI, Jacobsen JA, Flicek P, Dahl HA. Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly. Sci Rep. 2019;9:17716.
Near TJ, Eytan RI, Dornburg A, Kuhn KL, Moore JA, Davis MP, Wainwright PC, Friedman M, Smith WL. Resolution of ray-finned fish phylogeny and timing of diversification. Proc Natl Acad Sci U S A. 2012;109:13698–703.
Betancur RR, Broughton RE, Wiley EO, Carpenter K, Lopez JA, Li C, Holcroft NI, Arcila D, Sanciangco M, Cureton II JC et al The tree of life and a new classification of bony fishes. PLoS Curr. 2013; 5:ecurrents.tol.53ba26640df26640ccaee26675bb26165c26648c26288.
Igarashi Y, Zhang H, Tan E, Sekino M, Yoshitake K, Kinoshita S, Mitsuyama S, Yoshinaga T, Chow S, Kurogi H, et al. Whole-genome sequencing of 84 Japanese eels reveals evidence against panmixia and support for sympatric speciation. Genes (Basel). 2018;9:474.
Jansen HJ, Liem M, Jong-Raadsen SA, Dufour S, Weltzien FA, Swinkels W, Koelewijn A, Palstra AP, Pelster B, Spaink HP, et al. Rapid de novo assembly of the European eel genome from nanopore sequencing reads. Sci Rep. 2017;7:7213.
Henkel CV, Dirks RP, de Wijze DL, Minegishi Y, Aoyama J, Jansen HJ, Turner B, Knudsen B, Bundgaard M, Hvam KL, et al. First draft genome sequence of the Japanese eel, Anguilla japonica. Gene. 2012;511:195–201.
Pavey SA, Laporte M, Normandeau E, Gaudin J, Letourneau L, Boisvert S, Corbeil J, Audet C, Bernatchez L. Draft genome of the American eel (Anguilla rostrata). Mol Ecol Resour. 2017;17:806–11.
Howe K, Clark MD, Torroja CF, Torrance J, Berthelot C, Muffato M, Collins JE, Humphray S, McLaren K, Matthews L, et al. The zebrafish reference genome sequence and its relationship to the human genome. Nature. 2013;496:498–503.
Star B, Nederbragt AJ, Jentoft S, Grimholt U, Malmstrom M, Gregers TF, Rounge TB, Paulsen J, Solbakken MH, Sharma A, et al. The genome sequence of Atlantic cod reveals a unique immune system. Nature. 2011;477:207–10.
Jones FC, Grabherr MG, Chan YF, Russell P, Mauceli E, Johnson J, Swofford R, Pirun M, Zody MC, White S, et al. The genomic basis of adaptive evolution in threespine sticklebacks. Nature. 2012;484:55–61.
Aparicio S, Chapman J, Stupka E, Putnam N, Chia JM, Dehal P, Christoffels A, Rash S, Hoon S, Smit A, et al. Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes. Science. 2002;297:1301–10.
Jaillon O, Aury JM, Brunet F, Petit JL, Stange-Thomann N, Mauceli E, Bouneau L, Fischer C, Ozouf-Costaz C, Bernot A, et al. Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype. Nature. 2004;431:946–57.
Zebrafish Information Network [http://zfin.org/]. Accessed 25 Mar 2019.
Baldauf SL. Phylogeny for the faint of heart: a tutorial. Trends Genet. 2003;19:345–51.
Bergsten J. A review of long-branch attraction. Cladistics. 2005;21:163–93.
Ensembl: Fugu (Takifugu rubripes) genome database [http://www.ensembl.org/Takifugu_rubripes/Info/Annotation]. Accessed 15 Mar 2019.
GenBank: Atlantic cod (Gadus morhua) chromosome level assembly, GFC_902167405 [https://www.ncbi.nlm.nih.gov/assembly/GCF_902167405.1/]. Accessed 15 Oct 2019.
Ensembl: Atlantic herring (Clupea harengus) chromosomal level assembly; database version 98.202; genebuild released Sept 2019; assembly Ch_v2.02, Apr 2019. [http://www.ensembl.org/Clupea_harengus/Info/Index]. Accessed 25 Oct 2019.
GenBank: Atlantic herring (Clupea harengus) genome assembly GCA_900323705 [https://www.ncbi.nlm.nih.gov/assembly/GCA_900323705.1]. Accessed 20 Sept 2019.
GenBank: Atlantic herring (Clupea harengus) chromosome level assembly GCA_900700415 [https://www.ncbi.nlm.nih.gov/assembly/GCA_900700415.1]. Accessed 1 Oct 2019.
Pettersson ME, Rochus CM, Han F, Chen J, Hill J, Wallerman O, Fan G, Hong X, Xu Q, Zhang H, et al. A chromosome-level assembly of the Atlantic herring - detection of a supergene and other signals of selection. Genome Res. 2019;29:1919–28.
O'Brien J, Al-Ubaidi MR, Ripps H. Connexin 35: a gap-junctional protein expressed preferentially in the skate retina. Mol Biol Cell. 1996;7:233–43.
GenBank: Atlantic herring (Clupea harengus) genome assembly GCA_000966335.1 [https://www.ncbi.nlm.nih.gov/assembly/GCF_000966335.1]. Accessed 1 Sept 2019.
Parra G, Bradnam K, Korf I. CEGMA: a pipeline to accurately annotate core genes in eukaryotic genomes. Bioinformatics. 2007;23:1061–7.
Simao FA, Waterhouse RM, Ioannidis P, Kriventseva EV, Zdobnov EM. BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics. 2015;31:3210–2.
Waterhouse RM, Seppey M, Simao FA, Manni M, Ioannidis P, Klioutchnikov G, Kriventseva EV, Zdobnov EM. BUSCO applications from quality assessments to gene prediction and phylogenomics. Mol Biol Evol. 2017;35:543–8.
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990;215:403–10.
BLAST [https://blast.ncbi.nlm.nih.gov/Blast.cgi]. Accessed 15 Oct 2019.
MUSCLE [https://www.ebi.ac.uk/Tools/msa/muscle/]. Accessed 5 Sept 2019.
Ensembl: Three-spined stickleback (Gasterosteus aculeatus) genome database; database version 98.1; genebuild last updated 2010; assembly Broad S1, Feb 2006. [https://www.ensembl.org/Gasterosteus_aculeatus/Info/Index]. Accessed 10 Sept 2019.
Huse SM, Huber JA, Morrison HG, Sogin ML, Welch DM. Accuracy and quality of massively parallel DNA pyrosequencing. Genome Biol. 2007;8:R143.
Ensembl: Tetraodon (Tetradon nigroviridis) genome database; database version 98.8; genebuild last updated May 2010; assembly Tetraodon 8.0, Mar 2007. [https://www.ensembl.org/Tetraodon_nigroviridis/Info/Index]. Accessed 28 Aug 2019.
Ensembl: Atlantic cod (Gadus morhua) genome database; database version 98.1; Genebuild released Aug 2011; assembly gadMor1, Jan 2010. [https://www.ensembl.org/Gadus_morhua/Info/Index]. Accessed 1 Sept 2019.
Nomura K, Fujiwara A, Iwasaki Y, Nishiki I, Matsuura A, Ozaki A, Sudo R, Tanaka H. Genetic parameters and quantitative trait loci analysis associated with body size and timing at metamorphosis into glass eels in captive-bred Japanese eels (Anguilla japonica). PLoS One. 2018;13:e0201784.
GenBank: Japanese eel (Anguilla japonica) genome assembly GCA_0035977225 [https://www.ncbi.nlm.nih.gov/assembly/GCA_003597225.1]. Accessed 15 Aug 2019.
Nakamura Y, Yasuike M, Mekuchi M, Iwasaki Y, Ojima N, Fujiwara A, Chow S, Saitoh K. Rhodopsin gene copies in Japanese eel originated in a teleost-specific genome duplication. Zoological Lett. 2017;3:18.
Bracamonte SE. Anguilla anguilla spleen and head kidney transcriptome [https://www.ncbi.nlm.nih.gov/bioproject/PRJNA419718]. Accessed 15 Aug 2019.
Pasquier J, Cabau C, Nguyen T, Jouanno E, Severac D, Braasch I, Journot L, Pontarotti P, Klopp C, Postlethwait JH, et al. Gene evolution and gene expression after whole genome duplication in fish: the PhyloFish database. BMC Genomics. 2016;17:368.
Perrier F, Bertucci A, Pierron F, Feurtet-Mazel A, Simon O, Klopp C, Candaudap F, Pokrovsky O, Etcheverria B, Mornet S, et al. Transcriptomic profiling responses in liver and brain tissues of European eel Anguilla anguilla after a gold nanoparticle trophic exposure [https://www.ncbi.nlm.nih.gov/bioproject/PRJNA432560]. Accessed 15 Aug 2019.
Tse WK, Sun J, Zhang H, Law AY, Yeung BH, Chow SC, Qiu JW, Wong CK. Transcriptomic and iTRAQ proteomic approaches reveal novel short-term hyperosmotic stress responsive proteins in the gill of the Japanese eel (Anguilla japonica). J Proteome. 2013;89:81–94.
Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016;33:1870–4.
Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: Molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol. 2018;35:1547–9.
SíK was supported by grants from the Faroese Research Council, the Fisheries Research Fund of the Faroe Islands, Statoil Føroyar, the Faroese Pelagic Organisation and the Danish Innovation Fund.
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All sequences were obtained from pre-existing databases and genome assemblies. No animals, or samples from animals, were handled in the context of the present work, and no approvals were required for this work.
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The authors declare that they have no competing interests.
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Human (Homo sapiens) connexins. Suppl. Figure 2. Mouse (Mus musculus) connexins. Suppl. Figure 3. Opossum (Monodelphis domestica) connexins. Suppl. Figure 4. GJC1like and GJA9 connexin sequences from other marsupials and platypus. Suppl. Figure 5. Zebrafish (Danio rerio) connexins. Suppl. Figure 6. Japanese pufferfish (Fugu; Takifugu rubripes) connexins. Suppl. Figure 7. Green spotted pufferfish (Tetraodon nigroviridis) connexins. Suppl. Figure 8. Three-spined stickleback (Gasterosteus aculeatus) connexins. Suppl. Figure 9. Atlantic herring (Clupea harengus) connexins. Suppl. Figure 10. Atlantic cod (Gadus morhua) connexins. Suppl. Figure 11. Japanese eel (Anguilla japonica) connexins. Suppl. Figure 12. Connexin39.2 (“gjd2like”) from mammals. Suppl. Figure 13. Comparisons of human “GJA4P” against connexin39.2 and GJA4. A. Alignment of conserved domains in human “GJA4P” (NG_026166) against connexin39.2 (“gjd2like”) in various species at protein level. B. Alignment of conserved domains in human “GJA4P” (NG_026166) against GJA4 (connexin37) from human and eel at protein level. Suppl. Figure 14. Expanded branches from the phylogenetic tree shown in Fig. 1. A. Expanded view of the mammalian and teleost GJA1 branch. B. Expanded view of mammalian and teleost GJA3 branch, and the associated teleost cx39.9. C. Expanded view of the mammalian and teleost GJA4 branch. D. Expanded view of the mammalian and teleost GJA5 branch. E. Expanded view of the mammalian and teleost GJA9 and GJA10 branches. F. Expanded view of the teleost cx34.5 and cx32.2 branches. G. Expanded view of the mammalian and teleost GJB1 branch. H. Expanded view of mammalian and teleost GJB2 and GJB6 branch, and teleost cx30.3 branches. I. Expanded view of the mammalian GJB3 and teleost cx35.4 branches. J. Expanded view of mammalian GJB4 and GJB5, and teleost cx34.4. K. Expanded view of the mammalian and teleost GJB7 branch. L. Expanded view of the teleost cx28.6 group, and its relationship with GJB3/GJB4/GJB5. M. Expanded view of eutherian GJC3 and marsupial GJC1like and GJC2like branches. N. Expanded view of mammalian and teleost GJC1 and teleost cx43.4 branches. O. Expanded view of mammalian and teleost GJC2, and its relationship with GJC1 and cx43.4. P. Expanded view of mammalian and teleost Cx39.2 branch. Q. Expanded view over the central GJD2 complex. R. Expanded view of mammalian and teleost GJD3 branch. S. Expanded view of mammalian and teleost GJD4 branch. T. Expanded view of teleost cx36.7 branch. Suppl. Figure 15. Compressed phylogenetic tree illustrating long-branch attraction between gjc3, gjd4 and gje1 groups. Suppl. Figure 16. Searching for positions of connexins lacking in chromosome assemblies. A. Problem in cod assembly of chromosome 20 at assumed position of gja5. B. Alignments with sequences from herring and stickleback point to the same area on cod chromosome 21, indicated expected position of gja10-cx52.6. C. Alignments of herring and stickleback scaffolds containing cx52.6. Suppl. Figure 17. A homogeneous and consistent nomenclature for gap junction protein genes. Suppl. Figure 18. Schematic outline of the major procedures.
Statistical support for clade grouping. Suppl. Table 2. Parameter overview for statistical analyses of phylogenetic trees. Suppl. Table 3. Comparison between zebrafish connexin sequences from Ensembl and GenBank. Suppl. Table 4. Comparison between Fugu connexin sequences from Ensembl and GenBank. Suppl. Table 5. Comparison between cod connexin sequences from the Ensembl and GenBank assemblies. Suppl. Table 6. Comparison between herring connexin sequences from the GenBank genome assembly predictions and the Ensembl chromosomal level assembly predictions. Suppl. Table 7. Naming of connexin genes in Ensembl and GenBank. Suppl. Table 8. Percentages of amino acid identities between conserved domains in mammalian Cx39.2, including human “GJA4P”-NG_026166, and eel cx39.2 (one of the “gjd2like” sequences). Suppl. Table 9. Human GJA4P is more similar to GJD2like (connexin39.2) than GJA4 at nucleotide level. Suppl. Table 10. Ohnology among teleost connexins.
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Mikalsen, SO., Tausen, M. & í Kongsstovu, S. Phylogeny of teleost connexins reveals highly inconsistent intra- and interspecies use of nomenclature and misassemblies in recent teleost chromosome assemblies. BMC Genomics 21, 223 (2020). https://doi.org/10.1186/s12864-020-6620-2
- Genome duplication
- Phylogenetic trees