The significance of alternative transcripts for Caenorhabditis eleganstranscription factor genes, based on expression pattern analysis
© Craig et al.; licensee BioMed Central Ltd. 2013
Received: 29 December 2012
Accepted: 9 April 2013
Published: 15 April 2013
Sequence-specific DNA-binding proteins, with their paramount importance in the regulation of expression of the genetic material, are encoded by approximately 5% of the genes in an animal’s genome. But it is unclear to what extent alternative transcripts from these genes may further increase the complexity of the transcription factor complement.
Of the 938 potential C. elegans transcription factor genes, 197 were annotated in WormBase as encoding at least two distinct isoforms. Evaluation of prior evidence identified, with different levels of confidence, 50 genes with alternative transcript starts, 23 with alternative transcript ends, 35 with alternative splicing and 34 with alternative transcripts generated by a combination of mechanisms, leaving 55 that were discounted. Expression patterns were determined for transcripts for a sample of 29 transcription factor genes, concentrating on those with alternative transcript starts for which the evidence was strongest. Seamless fosmid recombineering was used to generate reporter gene fusions with minimal modification to assay expression of specific transcripts while maintaining the broad genomic DNA context and alternative transcript production. Alternative transcription factor gene transcripts were typically expressed with identical or substantially overlapping distributions rather than in distinct domains.
Increasingly sensitive sequencing technologies will reveal rare transcripts but many of these are clearly non-productive. The majority of the transcription factor gene alternative transcripts that are productive may represent tolerable noise rather than encoding functionally distinct isoforms.
Knowledge of the control of gene expression by complex regulatory networks acting at multiple levels is central to an understanding of metazoan development. Transcription factors, with the ability to distinguish between genes through their sequence-specific DNA-binding activity, have a key role at the primary level of gene expression, transcription. The large proportion of the genome devoted to encoding transcription factors increases as the size of the genome increases, highlighting their significance to biological complexity, and is around 5% for metazoans . Alternative transcripts from these genes may increase the complexity of the transcription factor complement still further . Increasingly sensitive sequencing technologies are revealing increasing numbers of alternative transcripts but it is unclear how much these add to transcription factor functionality. Transcription factor regulation of transcription factor genes is at the very heart of regulatory networks controlling expression of the genome. The complexity of interactions within transcription factor regulatory networks , further complicated by alternative isoforms, means that their comprehension depends on a more holistic view than the investigation of a single transcription factor can provide. The anatomical simplicity of the model system Caenorhabditis elegans provides a good subject for such systems scale analyses.
An extensive bioinformatics study, based on gene ontology and on DNA sequence predicted to encode known DNA-binding domains, identified 938 potential transcription factor genes in the C. elegans genome [4, 5]. Many of these loci, however, are annotated as producing more than one transcription factor isoform and so significantly more than 938 transcription factors may potentially be encoded in the C. elegans genome. A gene can have alternative promoters, alternative transcription termination or undergo alternative splicing to encode discrete transcripts with distinct protein-coding regions. Approximately 15% of C. elegans transcription factor genes were identified as alternatively spliced . This may be an under-estimate as the proportion of all C. elegans genes predicted or confirmed to encode alternative transcripts has increased from around 10% [6, 7] to 25%  in recent years as the sensitivity of techniques has increased. The number of potential alternative transcripts for transcription factor genes is likely to increase still further, although how many of these transcripts actually encode functional distinct transcription factor isoforms or are simply noise in the system is not yet clear.
It may be anticipated that alternative transcription factor isoforms would be produced for distinct purposes. The different modes of transcript production could allow distinct expression patterns with consequent distinct distributions of the transcription factor isoforms encoded by a single gene, for distinct functions in different sets of cells. Alternatively, the different isoforms encoded by a single gene might have different functions in the same cells. Through interactions with different co-factors, mediated by alternative protein domains, or even through differences in the sequence recognition specificity of the DNA-binding domain, the different isoforms may regulate different sets of genes. In this case the different transcripts encoded by the transcription factor gene would show overlapping expression.
Gene expression patterns are most easily determined with single cell resolution, in terms of the largely invariant developmental cell lineage described for C. elegans, using reporter gene fusion technology. Historically this has involved the creation of reporter gene fusions with parts of the gene of interest within a plasmid context, as recently when specifically targeting alternative splicing in C. elegans. However, genes with alternative transcripts are typically larger than genes without as they include alternative exons and associated regulatory elements. To maximize the chances of preserving the alternative modes of expression the whole of the gene and its genomic environs should be included, with minimal alteration, in any reporter gene fusion meant to tackle this subject. Seamless recombineering  of fosmids is an approach that addresses these issues.
Recombineering allows the precise insertion of a reporter gene into approximately 40 kb genomic DNA fragments cloned in fosmids. The compact genome of C. elegans means such fosmids typically contain the gene of interest along with several flanking genes and therefore the gene is present within the broader DNA context present endogenously. Specific exons can be tagged with the reporter to reveal the cells in which particular alternative transcripts can be found. Furthermore, such manipulated fosmids can be subjected to subsequent further recombineering steps to change single base pairs and thereby specifically eliminate contributions of certain transcripts to reporter expression patterns with minimal alteration [11, 12].
C. elegans transcription factor genes thought to encode multiple transcription factor isoforms were selected for analysis. Prior evidence for the existence of alternative transcripts for these genes was assessed. Recombineering was then applied for each gene selected to create a range of corresponding reporter gene fusion arrangements. Reporter expression patterns were determined in C. elegans transformed with these fosmids to reveal if alternative transcripts tend to exhibit alternative spatio-temporal distributions in this species.
Results and discussion
Assessment of prior evidence for alternative transcription factor isoforms
Numbers of transcription factor genes encoding alternative isoforms
Number of transcription factor genes
No evidence for alternative transcripts
Alternative transcripts encode same protein
Alternative transcripts annotated to encode different isoforms
Alternative unique starting exon - strong evidence
Alternative unique starting exon - weak evidence
Nested alternative starts
Alternative terminal exon - strong evidence
Alternative terminal exon - weak evidence
Non-constitutive internal exon - strong evidence
Non-constitutive internal exon - weak evidence
Non-constitutive internal intron - strong evidence
Non-constitutive internal intron - weak evidence
Alternative splice site selection - strong evidence
Alternative splice site selection - weak evidence
Alternative transcripts by multiple mechanisms - strong evidence
Alternative transcripts by multiple mechanisms - weak evidence
Alternative transcript evidence considered invalid
In contrast to alternative transcriptional initiation, no convincing examples of transcription factor genes with variation in transcript end as the sole mechanism for generating alternative transcripts were found. The strongest examples of genes annotated as such in WormBase, 23 in number, proposed a single alternative exon, either internal or terminal, but typically based on a single EST. When the alternative exon is internal the theoretical open reading frame rapidly reaches a termination codon, well before the end of the annotated transcript, either within the alternative exon or because the translational reading frame is shifted from the correct reading frame in the immediate downstream exon. Nonsense-mediated decay (NMD) would be expected to degrade such transcripts . More commonly there is a single alternative terminal exon that is simply an extension of an exon, internal to the gene, into what would otherwise be intron. Two foreshortened transcripts of this type are annotated for nhr-104 (Figure 1C), one based on a single EST but the other based on several. Strikingly, however, for both foreshortened nhr-104 transcripts the final exons are closely followed by non-coding RNA genes (R11E3.14 and R11E3.16) that are transcribed from the opposite direction. It is tempting to speculate that colliding transcription complexes could lead to premature termination of nhr-104 transcription and the ESTs found. Similar scenarios are seen in many other C. elegans genes. Another striking example of alternative transcript ends is provided by nhr-88. The alternative transcript termination for nhr-88 is simply due to the presence of a transposable element that is sometimes included, leading to premature termination of the translational reading frame, and sometimes spliced out of the transcript. Again, to emphasize, the proteins encoded by such low abundance, aberrant, foreshortened transcripts may still be functionally important.
A number of C. elegans transcription factor genes are annotated with alternative transcripts generated solely by alternative splicing. Amongst these genes, the most distinct isoforms would arise through inclusion versus exclusion of entire internal introns or exons, e.g. pqn-21 and nhr-117 respectively (Figure 1D and E). The evidence for any transcription factor gene using a non-constitutive exon as the sole mechanism for creating an alternative transcript is weak, with just five examples and only one or two ESTs in support of the alternative transcript in each case. There are, however, six transcription factor genes where non-constitutive introns are annotated as the sole source of transcript variation and for three of these, F23F12.9, zip-1 and atfs-1, the evidence is strong with many ESTs in support. Alternative splicing that gives more subtle isoform differences occurs where it is simply splice site selection that appears to vary. There are 24 transcription factor gene annotations with donor or acceptor splice site selection as the sole mechanism of transcript variation, but for almost all of these the alternative splice sites are just 3, 6, 9 or 12 nucleotides apart, thereby retaining the translational reading frame. Furthermore, for most of these, and for all three genes with alternative splice sites slightly further apart, there are only one or two ESTs to support the existence of the alternative transcript. There is good EST evidence, however, for alternative transcripts for hmg-1.2, nhr-14, bed-1 and Y65B4BR.5, with just 3 or 6 nucleotide differences between the alternative splice sites for each. Although such small distinctions may lead to inclusion or omission of only one or two amino acids in the protein product, the structural and functional consequences could still be highly significant. Alternatively, these examples of splice site selection variation may still simply reflect tolerable noise in the expression of these genes. The fact that for all 24 examples the distinct transcripts differ by a number of whole codons, such that the translational reading frame is maintained, may only reflect fully translated transcripts not being substrates for NMD ; i.e. transcripts generated with alternative splice sites that do shift the translational reading frame would not be translated along their length, would be degraded by NMD and consequently would not have been detected.
For some C. elegans transcription factor gene annotations the derivation of alternative transcripts is more complex, involving combinations of the mechanisms above. The experimental evidence is strong for 9 such genes, although there are a further 25 for which the evidence is weaker. Strikingly, amongst the instances that are well supported, there are 7 genes with alternative exons and 4 with alternative transcript ends. As there are no well-supported instances of these mechanisms being the sole mechanisms for alternative transcript generation, perhaps such variations in C. elegans gene expression are interdependent or dependent upon alternative transcript initiation. Might selection of an alternative exon be dependent upon the transcript secondary/tertiary structure, with this in turn dependent upon the alternative transcript starts?
This left another 55 transcription factor genes for which the WormBase annotation as encoding distinct isoforms was discounted. Gene annotations with examples from each of the mechanisms for generating alternative isoforms were placed in this category. The generally low level of expression of transcription factor genes  does mean there is often little of the EST evidence needed to strongly support gene structures and makes it harder to distinguish biologically relevant transcription from background transcriptional noise. Therefore, the distinctions between a transcription factor gene likely encoding or possibly encoding or discounted from encoding alternative isoforms will not be sharp. Nevertheless, many genes were placed in the discounted category for good reason. For some the EST upon which an alternative transcript was based was most unlikely to be translated into a protein because of out-of-frame translation initiation codons in the proposed 5′UTR. For others, translation of the proposed transcript required use of a different translational reading frame from that encoding the transcription factor. Finally, for several genes the alternative annotated transcript simply corresponded to the primary unspliced transcript. But it remains possible that functionally significant isoforms may arise from genes in the discounted category, or even from those not yet even annotated as encoding distinct isoforms, either at low abundance or only under certain environmental conditions.
Transcription factor genes investigated
Molecular gene name
Genetic gene name
Alternative transcript annotation in WormBase
Alternative isoform encoding assessment
Comment on annotation
DNA binding domain *
WH - Fork, AT Hook
Complex; alternative promoters & exon +/−
EST evidence for alternative promoters, single EST for alternative internal exon
WH - RFX
nested transcripts only
ZF - DM
Complex; alternative promoters & splice site variation
nested transcripts only
ZF - C2H2 - 1 finger, WH - Fork
nested transcripts only
WH - Fork
Complex; alternative promoters, intron +/− & exon +/−
RT-PCR primer derived alternative start
ZF - C2H2 - 3 fingers
two ESTs for alternative internal exon
ZF - NHR
ZF - NHR
ZF - NHR
ZF - NHR
Complex; alternative promoters & transcript ends
nested transcripts only
WH - Fork
single EST for extra intron
ZF - C2H2 - 1 finger
nested transcripts only
ZF - C2H2 - 3 fingers
nested transcripts only
single EST for extra intron
ZF - C2H2 - 7 fingers
Complex; alternative promoters, exon +/− & splice site variation
nested transcripts, single EST for extra exon & splice site variant
ZF - C2H2 - 4 fingers
Complex; alternative promoters & exons +/−
HD - TALE
single EST for alternative internal exon
HD - POU
HD - PRD
ZF - C2H2 - 3 fingers
single EST for alternative unique exon
ZF - C2H2 - 3 fingers
Alternative promoters with distinct starting exons
For each transcription factor gene examined, alternative promoters with distinct starting exons drove fosmid based reporter expression in only partly similar patterns, patterns neither all identical nor all discrete. The simple model of alternative promoters being present to allow expression of either functionally equivalent transcription factors in different cells or functionally distinct transcription factor isoforms in the same cells did not apply. Different promoters in a single transcription factor gene had different strengths, contributing to different degrees to the level of expression, and appeared to be under the influence of the same enhancers. It is also possible that the common components arise independently from the alternative promoters operating in isolation, through distinct sets of cis-acting regulatory elements. Some of the promoters in transcription factor genes drove expression only in subcomponents of the expression pattern driven by other promoters of the same gene. Often the expression from these transcription factor gene promoters was very broad, in multiple tissue types and throughout development.
The significance of distinct promoters for a transcription factor gene was most easily assessed when the promoters were identified from the presence of distinct starting exons for the alternative transcripts. Reporter genes were inserted immediately after the initiation codon in the starting exon of each transcript and also before the termination codon common to all transcripts (Figure 1A). Expression patterns of the former were expected to sum to the expression pattern of the latter.
All three alternative transcripts annotated for vab-3, i.e. vab-3a, vab-3b and vab-3c, have unique starting exons. When gfp was inserted immediately before the termination codon shared by all three transcripts, reporter expression was observed quite broadly, throughout development in the hypodermis, in body wall muscle in the anterior, in head and ventral cord neurons, in the intestine and in the distal tip cells (WBID Expr9742). A similar if not identical expression pattern, but weaker, was observed when gfp was inserted immediately after the initiation codon for transcript b (WBID Expr9731). While the common exons of the three vab-3 transcripts lie in just over 2 kb of genomic DNA and the unique starts of transcripts b and c lie within the 1 kb upstream, the specific start of transcript a lies more than 10 kb away. Nevertheless, the promoter for transcript a appears to have a similar activity to the promoter for transcript b, but weaker again. When gfp was inserted after the initiation codon for transcript a, expression in head muscle and hypodermis were observed (WBID Expr9765). The absence of intestine and distal tip cell components may be due to the weakness of expression. Isolated promoter regions, as cloned in the Promoterome , typically drive much stronger reporter expression for transcription factors in comparison to insertion of the reporter into the whole gene . The Promoterome fragment for vab-3 transcript a  drove expression in the same components as observed with the other recombineered vab-3 reporter gene fusions, including the intestine and distal tip cells (WBID Expr7504). The common expression pattern is particularly noteworthy given that the Promoterome fragment assayed is just 2 kb of DNA from upstream of the transcript a start, well away from the common exons shared by all three transcripts and the start of the other two transcripts. Meanwhile, the promoter for transcript c, located between the common exons and the start of the other transcripts, drove stronger although still weak reporter expression but with a much more restricted distribution, in just a few head nerve cells (WBID Expr9757).
For several other transcription factor genes examined, at least one of the promoters defined by a unique starting exon also appeared to drive expression in the same pattern as the gene in its entirety. For both atf-7 and nhr-46, there are two promoters defined by unique starting exons, the most upstream of each looking dislocated from the rest of what are otherwise compact genes. Nevertheless, when gfp was inserted into either of the unique starting exons for atf-7, the same, strong, very broad specificity, reporter expression pattern, peaking in the L1 stage, was observed (WBIDs Expr9790/9808). For nhr-46, gfp inserted after the transcript a specific start codon, in the proximal of the two unique exons, gave the same expression pattern as when gfp was inserted before the termination codon common to all transcripts; again a broad distribution but peaking this time in the L2 stage (WBIDs Expr9816/9835).
For ztf-26 and egl-13, gfp inserted after the initiation codon of the a transcripts, in the more distal unique exon, gave apparently the same reporter expression as when gfp was inserted before the shared termination codon of each gene. While the expression of ztf-26 was broad, including nerve cells, hypodermis and muscle peaking in the L4 stage (WBID Expr9838), that for egl-13 was more restricted, limited to a few nerve cells in the head and tail, and weakly in body wall muscle, but through all postembryonic stages (WBIDs Expr9735/9745). Again, the Promoterome fragment for egl-13 transcript a  drove the same but much stronger reporter expression with detectable GFP production in vulval muscle as well as body wall muscle (WBID Expr7672). The recombineered reporter gene fusion to assay egl-13 transcript d, however, gave weak but clear expression in the region of the developing gonad, probably the developing vulval muscle (WBID Expr9746). The impression given is that promoters for egl-13 transcripts a and d both drive expression in the same cells, but with different strengths in different places, the very weak expression from promoter d being detectable in the developing vulva but not elsewhere, with the assay performed. For ztf-26 the recombineered reporter gene fusion for the second promoter, that for transcript b, reveals a subtle distinction in promoter activity that may be more temporal rather than spatial, with GFP expression peaking in the L1 stage (WBID Expr9844).
Alternative promoter activity was confirmed for two genes, F13H6.1 and klf-3, for which the EST evidence for the alternative promoter was considered weak. The unique starting exon of F13H6.1a was based on a single EST clone, yet gfp insertion after the initiation codon (WBID Expr 9727) gave the same strong reporter expression as insertion before the termination codon common to both F13H6.1 transcripts (WBID Expr9843). Although not specifically assayed F13H6.1b would not appear to contribute any additional components to this gene’s expression pattern. Exon 1 of transcript a of klf-3 (called mua-1 in earlier versions of WormBase) starts just a few nucleotides before exon 2 of transcript b, after which the two transcripts are identical. The experimental evidence for the transcript a start is an RT-PCR derived ORFeome  clone generated using a 5′ PCR primer that included nucleotides corresponding to that transcript start (WormBase). Nevertheless, insertion of gfp after either initiation codon or before the termination codon yielded reporter expression and with closely related patterns (WBIDs Expr9810/9814). The absence of the intestinal component for the transcript a specific fusion was the only difference suggesting the transcript b promoter drives the full expression pattern for klf-3.
The jun-1 gene has five promoters defined by unique starting exons and is probably expressed in all cells. The strong and broad expression driven by the jun-1 transcript a Promoterome fragment  (WBID Expr7681) made it difficult to be certain that there were no cells lacking GFP, but the reporter was expressed more strongly in some tissues than others. All five promoters were assayed by recombineering-mediated insertion of gfp immediately after each of the unique initiation codons (WBIDs Expr9763/9764/9768/9780/9782). Once more, and for every promoter, the recombineered reporter gene fusions gave much weaker GFP expression than observed previously with the corresponding Promoterome construct. However, for fusions reporting on the different jun-1 promoters, including that for transcript a, different components were emphasized with higher levels of expression and many components were shared in different combinations. The promoters for transcripts a and d appeared the strongest, while those for transcripts b and e were the weakest. Insertion of gfp upstream of the common termination codon gave the most widespread reporter expression for the recombineered fusions (WBID Expr9740). The impression given is that the broad expression of jun-1 is generated in an overlapping piecemeal fashion, different isoforms lacking specific distributions of functional significance and possibly expressed to some level in all cells.
For two of the genes assayed, nhr-23 and nhr-66, the two promoters defined by alternative starting exons did not appear to provide all the expression pattern components observed when the reporter was introduced before the common termination codon. While the hypodermal and neural expression was observed for the promoters of nhr-23 transcripts c/d and a (WBIDs Expr9749/9781), the intestinal expression component of the terminal fusion was lacking (WBID Expr9736). Fusions for the promoters of nhr-66 transcripts b and c (WBIDs Expr9750/9804) appeared to fail to drive the expression in the spermathecae or in the hypodermis and muscle throughout the body observed for other fusions (WBIDs Expr9766/9771). Weak reporter expression may again mean absence of expression components is simply due to the signal falling beneath background. The gene models for both of these genes do, however, have additional nested transcripts that could provide the missing components.
The daf-16 gene is annotated as having 4 different unique starting exons. However, daf-16 stretches over nearly 25 kb and was not contained fully in a single fosmid. Therefore, two overlapping fosmids were joined together by recombineering creating a fosmid with daf-16 at the centre of a 65 kb insert. Although working with such a large clone was not straightforward, gfp was successfully inserted in two places. First, an insertion immediately before the stop codon tagged all annotated transcripts. Second, an insertion immediately after the transcript d start codon tagged transcripts d, f and h, the three longest transcripts, with clustered 5′ ends 12 kb upstream of the rest of the gene. Both of these reporter gene fusions and a previous conventional transcriptional reporter gene fusion to just the 2 kb region immediately upstream of the start of transcript a, only 3 kb from the 3′ end of the gene , yielded at least very similar GFP expression patterns (WBIDs Expr9815/9833/7644). Broad GFP expression in many tissues but most strongly in nerve cells was observed from early embryogenesis through to the adult.
Alternative promoters with transcript starts located within exons of longer transcripts
Alternative promoters are also implied by gene model transcripts annotated to start within internal exons of longer transcripts (Figure 1B). Like transcripts with alternative unique first exons, such nested transcripts again share downstream exons and the termination codon. To assess the expression patterns of a nested transcript, gfp was inserted immediately after the proposed initiation codon. However, an extra base pair was simultaneously inserted upstream of the targeted initiation codon to shift the translational reading frame of, and eliminate reporter expression arising from, other transcripts within which the transcript of interest was nested. Alternatively or additionally, the recombineered fusion with gfp inserted before the termination codon was secondarily modified with single nucleotide changes in starting exons to successively eliminate reporter expression arising from alternative transcripts.
Typically, nested transcripts appeared expressed in the same pattern as the transcripts within which they were nested. For ref-2, insertion of gfp before the common termination codon or after the initiation codon for the longer transcript b or after the initiation codon for the nested transcript a but with translation from the upstream start disrupted, gave apparently identical reporter expression patterns (WBIDs Expr9812/9813/9829). This was quite a specific expression pattern consisting of the P blast cells and some of their immediate descendants, and a few nerve cells in the head and tail. For three other assayed genes with only nested alternative transcripts, sox-2, dmd-6 and pes-1, the expression pattern appeared to be the same for all recombineered reporter gene fusions created for each (WBIDs Expr9798/9801/9841, Expr9817/9820/9821 and Expr9729/9753). Although not every possible reporter gene fusion arrangement was investigated in these cases, the absence of differences implies that nested transcripts do not provide additional expression pattern components beyond those provided by the transcripts within which they are nested. Nevertheless, the nested transcripts do appear productive. The reporter expression patterns of sox-2 and dmd-6 were broad, including several tissue types, while that for the forkhead gene pes-1 was more developmentally restricted like ref-2.
The gene model for fkh-7 appears very similar to that for fkh-9. Most fkh-7 ESTs correspond to transcript b starting from exon 2. There is a small exon 1 far upstream starting transcript a and a small transcript c from the end of the gene. (A single-exon transcript, transcript d, is also annotated for the very end of fkh-7 but with a different translational reading frame altogether and was therefore ignored.) When gfp was inserted before the termination codon common to transcripts a, b and c, reporter expression was seen from embryo to adult, and in nerve cells, hypodermis, pharynx, muscle, spermathecae, vulva and intestine (WBID Expr9732); again very broad expression as for fkh-9. Levels of the nuclear-localized GFP varied between tissues with the weaker components only seen in the transgenic strains with the strongest expression. Reporter expression was observed but at a lower level when gfp was inserted after the initiation codon of transcript a (WBID Expr9733), or after the initiation codon of transcript b with insertion of an extra base pair to eliminate translation from further upstream such as for transcript a (WBID Expr9822). Nevertheless, the GFP distributions arising ostensibly from the promoters specific for transcripts a or b appeared the same as when all transcripts were terminally tagged. When exon 5 was disrupted in the terminally tagged reporter fusion, to block expression arising from transcripts a and b, broad expression of GFP continued to be observed, but with the nuclear localization lost (WBID Expr9831). The only remaining annotated transcript, transcript c, would encode a protein lacking the DNA-binding forkhead domain, consistent with the loss of nuclear-localization. However, when expression due to transcripts a and b was disrupted with a two base pair deletion in exon 2, in the terminally tagged construction, broad nuclear-localized reporter expression was retained (WBID Expr9773). These observations suggest an alternative promoter can drive production of another un-annotated transcript for this gene, including more exons than found in transcript c, at least if expression from upstream promoters is perturbed. But again the different isoforms arising from the nested transcripts of fkh-7 appear to be expressed in the same cells and the alternative promoters do not exist to confer expression in different locations.
Additional nested transcripts are identified in WormBase models for some of the genes considered in the preceding section, with alternative promoters identified from unique starting exons. Although not specifically assayed, the similarity of expression patterns for reporter gene fusions that were recombineered suggests that the nested transcript c for both nhr-46 and ztf-26 would not contribute any novel expression pattern components. The expression patterns for nested transcripts for three other genes of this type, egl-13, nhr-23 and nhr-66, were specifically investigated. Again gfp was inserted immediately after the proposed initiation codon by recombineering with simultaneous insertion of a single extra base pair to eliminate translation arising from further upstream. From this approach, the egl-13 transcript c appears to be expressed in the same pattern as transcript a within which it is nested (WBIDs Expr9800/9745). For nhr-23, gfp inserted into the unique starting exons of transcripts a and c/d failed to yield the clear intestinal component observed when gfp was inserted into the common final exon (WBIDs 9736/9749/9781). An assay aimed specifically at transcript b/f, nested within transcript a, did yield intestinal GFP, but inconsistently (WBID Expr9760). We considered the evidence for annotated nhr-23 transcript e, nested within all the other transcripts, to be very weak so this transcript was not specifically assayed but presumably there is another transcript for nhr-23 that is responsible for the intestinal component and this could be transcript e. However, for nhr-66 the specific assay of transcript a yielded reporter expression (WBID Expr9771) very similar to that for gfp insertion in the shared terminal exon (WBID Expr9766) and much stronger than the extremely faint expression observed for transcript c (WBID Expr9804) in which transcript a is nested. EST support is also much stronger for transcript a than transcript c suggesting that the nested transcript a is actually the primary transcript.
The nested transcripts of egl-44 were investigated, although the alternative splice site selection also in the annotation for this gene was not. Insertion of gfp, either before the termination codon common to all transcripts or after the start codon of the longest transcript (transcript a), yielded broad nuclear-localized expression (WBID Expr9761/9769). In contrast, insertion of the reporter immediately after the start codon for transcripts starting with the second exon, transcripts b/c, yielded very weak expression of much more limited distribution and lacking sub-cellular localization (WBID Expr9752). The extra base pair to disrupt reporter expression arising from translation from further upstream, had to be inserted immediately between the splice acceptor and the initiation codon and, therefore, could have perturbed expression for transcripts b/c more dramatically, as for fkh-9b. Nevertheless, nested transcripts for egl-44 do not appear to add significantly to the expression of this gene.
Optional internal introns and exons
While the bioinformatic analysis yielded few likely examples of alternative transcription factor isoforms being derived solely from alternative splicing, a sample of these were selected for investigation. The significance of alternative transcripts derived from alternative splicing could be tested by disrupting reporter expression that is specifically dependent upon translation across the optional protein-coding region. The reporter gene was inserted by recombineering at the start and end of the gene to observe expression due to all transcripts. Subsequently, single base pairs could then be inserted by recombineering into the optional exon or optional intron within the recombineered reporter fusion with gfp inserted before the termination codon. Such minimal manipulation should shift the translational reading frame and disrupt reporter expression arising from inclusion of that optional region in the transcript. Expression resulting from transcripts with the optional exon skipped or the optional intron spliced out should remain. Comparison of the remaining reporter expression to the expression observed for all transcripts could reveal the significance of the alternative splicing.
Three genes with potentially non-constitutive introns, atfs-1, spr-3 and pqn-21, were selected. While gfp inserted immediately before the stop codon for spr-3 only drove infrequent nuclear-localized reporter expression in individual embryonic cells (WBID Expr9762), the same type of fusion for atfs-1 gave reproducible and broad non-nuclear-localized GFP (WBID Expr9743). A lack of reporter expression for conventional full-length spr-3 fusions was also observed previously . The atfs-1 result is consistent with the similar expression pattern described for a conventional reporter gene fusion and this transcription factor only becoming nuclear-localized in response to stress . However, no reporter expression was observed when gfp was inserted immediately after the start codon of atfs-1 and spr-3 (WBID Expr9728/9770). As a consequence, the significance of the alternative transcripts for these two genes was not explored further.
Few examples of transcription factor isoforms being generated solely by alternative splicing were apparent from the bioinformatic analysis and the evidence therein was quite weak. Experimental investigation of five such genes failed to yield any evidence in support of such mechanisms being in operation for these genes.
Alternative transcripts generated by multiple mechanisms
In contrast, there were 8 transcription factor genes for which there was good prior evidence for alternative splicing occurring in combination with the use of alternative promoters, and a further 19 for which the evidence for such was weaker. Expression patterns of 3 of the former and 2 of the latter genes were investigated. A few further genes appeared to combine alternative splicing with alternative termination but these were not examined experimentally.
The gene model for daf-19 also proposes three alternative transcriptional starts (Figure 6B). The shortest transcript (transcript c encoding DAF-19M) arises from the most downstream promoter and begins with a unique exon. The transcript from the middle promoter (transcript d encoding DAF-19C), however, starts in an exon designated as optional for the longest transcripts (transcript b with the exon, transcript a without) and is therefore nested. GFP expression was observed upon insertion of the reporter after each of the three alternative start codons (WBID Expr9747/9767/9796). The fusion to assay the nested transcript, transcript d, included a frame-shifting base pair insertion before the initiation codon to shift the reading frame and eliminate contributions to reporter expression from the most upstream promoter. Activity was therefore revealed for all three promoters, although the reporter expression for the nested transcript’s promoter was weak. The reporter expression patterns arising from the three promoters also appeared nested in that, in hermaphrodites, the most upstream promoter drove broad expression in neural and, weakly, in non-neural cells, the middle promoter drove expression in only neural cells but in the head and tail, while the most downstream promoter drove only neural expression and only in the head. Any subtle distinctions in these expression patterns within the neural system corresponding to the distinct daf-19 transcript distributions described by others [24, 25] would have needed more thorough analysis. The previously described male-specific head neuron expression for transcript c , the daf-19 transcript labelled simply as male-specific in WormBase, was observed with the recombineered fusion specific for F33H1.1c (WBID Expr9747). However, strong male specific neural expression was also seen with fusions recombineered specifically for F33H1.1a/b, but in the tail (WBID Expr9767). Nevertheless, the distinct distributions of isoforms revealed previously by immuno-histochemistry using antibodies specific to the DAF-19 N and C-terminal regions  could be entirely due to differences in expression of the non-nested transcripts.
There are four transcript starts annotated for hlh-30 (Figure 6C). One, for transcripts d/e, is nested from the second exon of the longest transcripts, transcripts b/c. Transcripts a/f/g start with an exon in the long intron of, and not included in, those four transcripts starting further upstream. Even further downstream in the gene model, there is an optional exon, included in transcripts a/c/d/g in which another nested transcript, transcript h, also begins. Finally, the second to last intron is optional, creating an alternative earlier translation termination when this splicing event is skipped, in transcript g. The annotation proposes 8 transcripts in total, as not every permutation is included.
When gfp was inserted before the final stop codon of hlh-30 or after the start codons of the non-nested transcripts, i.e. transcripts b/c and a/f/g, the same broad, strong, nuclear-localised reporter fluorescence was observed in many tissues and from early embryogenesis onwards (WBID Expr9739/9774/9785). When the reporter was inserted after the initiation codon of transcripts d/e, the nested transcripts starting from the second exon, GFP was again expressed, and with a broad distribution, but was no longer nuclear-localized (WBID Expr9775). However, this fusion would also have tagged expression from transcripts b/c starting further upstream. Therefore, the non-nuclear-localization may arise from disruption of functionality of HLH-30b/c::GFP fusion proteins and, as the cellular distribution is indistinguishable, this expression does not provide support for transcripts d/e. An attempt to test if the alternative splicing was responsible for distinct distributions of HLH-30 isoforms was equivocal; insertion of gfp into the optional exon yielded no reporter expression (WBID Expr9776), suggesting that this exon is not included in functional transcripts, despite strong EST evidence of frequent inclusion of this exon. Nevertheless, the two distinct hlh-30 promoters clearly drove strong expression of two HLH-30 isoforms in apparently the same cells throughout the soma.
There is good EST evidence for two alternative starting exons and two mutually exclusive internal seventh exons for unc-62 (Figure 6D). The EST evidence in support of the three further nested transcripts in the gene model, each with their own transcription start points, is weaker. There were no fosmids available with the 13.5 kb gene centrally located with which to examine unc-62 expression. Therefore the reporter was inserted by recombineering into two different fosmids, one extending further upstream of unc-62, the other further downstream, but both including at least 2 kb either side of the protein coding region. Both fosmids appeared to contain all essential cis-acting regulatory elements controlling unc-62 expression as equivalent constructions in the two fosmids gave apparently the same reporter expression patterns. Insertion of the reporter immediately upstream of the termination codon common to all transcripts yielded nuclear-localized GFP in multiple discrete components including nerve cells, muscle cells, the vulva, the hypodermal seam cells and the intestine, and from embryogenesis to the adult (WBID Expr9786/9837). However, the relative strength of signal in the different expression components was noted to vary between different independent transgenic lines created with any particular fosmid-based reporter gene fusion. A possible interpretation is that unc-62 is subject to complex self-regulation such that reporter fusion expression is sensitive to subtle variations in configuration of a few of the transgene copies present in the tandem extra-chromosomal arrays generated during C. elegans transformation. To examine expression arising specifically from the different transcripts the gfp reporter was inserted into one of the alternative first or seventh exons, or these non-constitutive exons were specifically disrupted by insertion of a single extra base pair in the 3′ reporter gene fusion fosmid constructions. All such fusions drove gfp expression in multiple locations suggesting that the different unc-62 transcripts are not responsible for discrete expression pattern components and all are expressed in many locations (WBID Expr9777/9778/9787/9793/9811/9818/9819/9825/9839/9845). Indeed reporter expression was still observed in multiple components when both unique first exons were disrupted by recombineering of the 3′ reporter fusion (WBID Expr9832/9797), so these are not the only functional transcriptional starts. One other transcript, nested transcript g, was shown to be functional as when gfp was inserted immediately after the start codon, with a single base pair insertion to disrupt any translation arising from further upstream, multiple reporter expression components were again observed (WBID Expr9840). There appear to be many alternative unc-62 transcripts each expressed in multiple components that are substantially, if not completely, overlapping.
The nurf-1 gene model annotation (Figure 6E) has been modified repeatedly within WormBase (with some consequent confusion in transcript names) and has a particularly complex structure with 11 annotated transcripts, multiple promoters and two points of transcript termination. The 17kb nurf-1 protein coding region was not contained in any single fosmid and so, as with daf-16, two fosmids were joined together by recombineering to reconstitute the whole unit before inserting the reporter. In addition to transcripts running through the entire gene model, there are transcripts for both halves of the gene that overlap in the two central exons. Insertion of gfp after the most upstream nurf-1 start codon (in WS230), for transcripts a/b/c/i/k, yielded very broad nuclear-localized fluorescence (WBID Expr9824). This expression pattern represents expression arising for the transcripts from just the 5′ half of the gene plus the transcripts running the entire length of the gene. An essentially equivalent pattern of reporter expression was observed with gfp inserted at the end of the central alternative terminal exon (WBID Expr9826), which only tags transcripts b/i/k from the 5′ half of the gene, suggesting that transcripts running the whole length of the gene add little to the gene’s expression. Furthermore, insertion of gfp after the second annotated start codon, which initiates translation for transcripts d/h from across the 3′ half of the gene, also gave the same expression pattern (WBID Expr9827). As this construction would report on expression of transcripts from across just the 5′ as well as just the 3′ gene halves and the full-length transcripts, this observation suggests that the transcripts across the whole 3′ half of the gene also contribute little to the gene’s expression. There are a series of alternative transcription starts annotated close to the 3′ end of the gene, for transcripts e, f/g and j. Insertion of gfp after the initiation codon in the exon unique to transcript e yielded no detectable reporter expression (WBID Expr9828). Similarly, no expression was observed upon insertion of gfp immediately before the stop codon of transcript h, with the last exon in a different reading frame from all other transcripts for the 3′ half of the gene due to a proposed alternative splice. Transcripts e and h may not be functionally significant. Insertion of gfp after the initiation codon in the exon unique to transcripts f/g, however, yielded a strong signal that, in contrast to the other positive results for nurf-1, was not nuclear-localized, with a slightly more restricted tissue distribution (WBID Expr9842). The implication is that nurf-1 primarily encodes two gene products, one corresponding to the 5′ half of the gene, which is nuclear-localized, and one to only the last 5 exons, which is not nuclear-localized, but occasional failure to terminate transcription centrally leads to rare transcripts across the entire gene. This interpretation is consistent with the distribution and abundance of nurf-1 ESTs (WormBase). Nevertheless, the conservation of the entire nurf-1 transcription unit organization in other animals suggests that the rare full-length transcripts are functionally significant, even if not very abundant.
Although the majority of GFP fusions made in this study gave detectable expression in vivo, neither of those tagging an alternative translational reading frame did. In both cases assayed, for syd-9 and nurf-1, the alternative reading frame runs through the final exon, is based on a single EST, and could simply reflect a rare splicing error. Functional alternative translational reading frames are seen frequently in viral genomes, with severe size constraints, but rarely in animal genomes where there is much less pressure to use the genome in an efficient manner.
The significance of alternative transcripts for the expression of C. elegans transcription factor genes was explored. Expression patterns were determined in vivo for 121 gfp reporter fusions, constructed in fosmids by recombineering to maintain the broad genomic DNA context, for 29 genes. We began with a thorough assessment of the gene models as annotated in WormBase. A gfp reporter was inserted seamlessly at specific points in each gene, with or without subsequent minimal manipulations, so as to assess the contributions of different transcripts to the complete expression pattern of each gene.
The alternative transcripts of C. elegans transcription factor genes encoding multiple isoforms differ most frequently in their starting points, their 5′ ends. Transcripts with distinct first exons presumably arise from distinct promoters. Strikingly almost all such genes yielded either a very broad or constitutive reporter gene fusion expression pattern, in marked contrast to the spatially and/or temporally restricted expression patterns seen more frequently in a prior, unfocussed screen of C. elegans transcription factor gene expression patterns . Only egl-13, amongst the 17 examples examined, yielded a more restricted expression pattern but this still included nerve cells, body wall muscle cells and vulval muscle cells, through postembryonic development. The full broad gene expression pattern of each gene appeared driven by at least one of the promoters in every example, with other promoters driving expression in sub-components. There are hints from close observation of the reporter expression that this may actually reflect each promoter driving expression in all of the different components for a particular gene but at markedly different levels. Such a mode of expression could arise from the promoters being quite general, but regulated by multiple enhancer elements for different expression components distributed across the gene, their influence on each promoter varying, perhaps with proximity.
The other way in which transcripts for a gene can differ at their 5′ ends is when the transcripts are nested, with the starts of shorter transcripts lying within internal exons of longer transcripts. Again, five of the seven genes examined which had purely nested alternative transcripts yielded broad expression. It may have been anticipated that often such nested transcript annotations would simply reflect artefactual ESTs arising from truncated first strand cDNA synthesis with no biological relevance. However, each assay specific for a nested transcript, with elimination of expression arising from further upstream, yielded reporter expression. This suggests that typically the nested transcripts do indeed contribute to the expression of a gene and could have their own promoters. Nevertheless, the expression patterns observed for the nested transcripts typically appeared the same as for the transcripts within which they were nested. The single exception to this was nhr-23 although the additional intestinal component observed with the reporter fusion for the nested transcript was only seen infrequently. In general, therefore, the nested transcripts may arise simply from transcription starting from the shared upstream promoter, with trans-splicing onto an internal, downstream splice acceptor to generate the shorter transcript(s). Such nested transcripts would not provide differential expression of transcription factor isoforms.
Dramatically distinct transcription factor isoforms would be generated if alternative transcripts arose from inclusion versus exclusion of optional introns or exons. However, examination of all our reporter expression patterns failed to provide evidence to support such an arrangement as the sole mechanism operating for a transcription factor gene. While alternative splicing of C. elegans genes has received considerable attention (reviewed in ) this mode of generating alternative isoforms appears of less importance for transcription factor genes and indeed few C. elegans transcription factor genes are annotated with such an organization. Furthermore, for 3 of the 5 genes specifically investigated here in this regard, insertion of the reporter after the annotated initiation codon failed to yield reporter expression, a result not seen for any of the other genes examined. The concerns over the gene models that such results raise was vindicated, at least for unc-86, with the subsequent revision of this gene’s start in WormBase revealing that the reporter had actually been inserted upstream, outside of the real protein coding region. But this only serves to emphasize the lack of certainty in gene structures that exists for genes, like those encoding transcription factors, with low levels of expression and consequent poor EST evidence. The gene models have been revised for 10 of the 29 assayed genes in the four years between WS190 and WS230. In addition, reporter expression observed for pqn-21 and nhr-117, the other 2 genes of the 5 examined here, yielded no support for alternatively spliced transcripts. In both cases, the coding region annotated as optional appeared to be used constitutively, whether this is an exon (nhr-117) that is spliced into, or an “intron” (pqn-21) that is not spliced out of, the final transcript.
Reporter analysis did show alternative exons were utilised for unc-62, but in combination with other modes of alternative transcript generation and, uniquely, the alternative internal exons were mutually exclusive rather than optional. Further complexity in unc-62 expression, beyond generation of the four previously characterized transcripts , is implicated: first, from the variability of expression pattern between different transgenic lines created with the same reporter gene fusion; second, from the continuation of reporter expression even after the coding regions of both of the mutually exclusive alternative first exons were disrupted. The latter expression could have arisen from one or more of the nested transcripts, one of which was confirmed to be functional. The promoter driving expression of the nested transcript could lie upstream of any of the first three exons, the uncertainty introduced by the complications of trans-splicing. Despite the range of transcripts encoded, unc-62 expression was broad with multiple components and the components attributed to different transcripts appeared substantially overlapping if not identical. It was impossible to associate specific transcripts with specific components suggesting whatever the importance of having alternative transcripts, it is not to allow different UNC-62 isoforms to be expressed in distinct sets of cells.
Similarly, none of the other genes, with alternative transcripts generated by multiple mechanisms that were examined, yielded evidence for non-overlapping expression patterns for different isoforms. For daf-19, the expression patterns for the downstream promoters and nested transcript appeared to overlap substantially with the broad expression domain of the upstream promoter. For hlh-30, both distinct promoters gave the same broad expression, with the nested transcripts encoding fusion proteins that were no longer nuclear-localized. The complexity of the syd-9 annotation may be misleading in that only one transcript appeared to yield reporter expression. Even for nurf-1, with its clearly distinct yet linked halves, expression is very broad, at least for the first half of the gene.
The general impression gained from this extensive analysis of a significant sample of C. elegans transcription factor genes is that structural qualities of this class of proteins, combined with the broad expression of certain members, simply allows alternative gene transcripts to be tolerated. It has been noted previously that, compared to mammals, C. elegans tends to have fewer genes with alternative transcripts and fewer alternative transcripts per gene . This distinction is now emphasized with the interpretation that, even when multiple transcripts are expressed from a single C. elegans gene, these may all be expressed similarly and lack distinct functions in distinct cells, at least for transcription factor genes. In Drosophila melanogaster shadow enhancers have been identified, apparently to improve precision and reproducibility of gene expression patterns . While these shadow enhancers are not envisaged to cause expression of alternative transcripts encoding distinct protein isoforms, the alternative promoters for C. elegans transcription factor genes could have a similar value for robustness of gene expression.
The low level of expression of transcription factor genes means that background noise makes up a larger fraction of the transcripts produced and increases the difficulty of distinguishing physiologically relevant transcripts for gene models. Simple detection of alternative transcripts, with the increasingly sensitive techniques available [29, 30], need not mean that a transcript is functional or that production of alternative transcripts by a gene is physiologically important. This consideration applies to other organisms beyond C. elegans. Claims of functionality of alternative transcripts should depend on observation of phenotypes specifically dependent on the integrity of the proposed coding region of the alternative isoforms. Indeed reporter expression alone also does not reveal biological function for an alternative isoform. However, notwithstanding the difficulties arising from functional redundancy, complementation of gene knockouts with the subtly manipulated fosmids described here could address these questions of functional significance.
Fosmid clones were obtained from a C. elegans fosmid library (Source BioScience Life Sciences) of approximately 30-40 kb genomic DNA inserts cloned in the pCC1FOS vector. Fosmids, maintained at low copy number in EPI300 E. coli, were grown in overnight LB cultures containing 0.01% arabinose to induce clone copy number. DNA was extracted using either the FosmidMAX kit (Epicentre) or the QIAprep Spin Miniprep kit (Qiagen) and fosmid identity was confirmed by restriction digest.
Recombineering was carried out using a slightly modified protocol to that described previously . Fosmid DNA was electroporated into either EL350 (Invitrogen) or MW005  strains of E. coli and electrocompetent cells were prepared with incubation at 42°C to induce the Red functions. For each gfp insertion, a specific rpsL-tetA(C) cassette (RT cassette) was generated by PCR from a template containing the cassette flanked by the first and last 50 nucleotides of the GFP coding sequence (fUL#SB29 ) and maintained in the pCC1FOS vector without copy control induction. The primers consisted of 50 nucleotides of gene-specific sequence flanking the desired site of insertion, known as the homology arms (HAs), plus 20 nucleotides directed at the very 5′ or 3′ ends of the gfp present in the template. An extra nucleotide was inserted immediately before the initiation codon when the translational reading frame was to be shifted for assaying nested transcripts. For unc-62, substitutions were used to create in-frame stop codons in the alternative first exons that would knock out expression from transcripts containing the exon. To eliminate expression arising from transcripts containing the alternative internal exons in unc-62, a single base pair was inserted within that exon to create both an in frame stop codon and a translational frame shift. For introducing point mutations, the RT cassette was amplified in the same manner and with the same template except that: the primers consisted of 50 nucleotide HAs plus the first or last 20 nucleotides of the RT cassette sequence rather than the flanking GFP; and the HAs matched genomic DNA segments 200–300 base pairs apart, resulting in the replacement of this section by the RT cassette. PCR was performed with Platinum Taq DNA Polymerase High Fidelity (Invitrogen) and the products purified with a QIAquick Gel Extraction Kit (Qiagen). After electroporation and selection for RT cassette insertion, potential positive clones were re-streaked and screened directly by PCR with primers flanking the insertion point.
Single tetracycline-resistant RT-positive clones were used to prepare electrocompetent cells for the second recombineering step, again with Red functions induced. GFP coding sequence (with introns) was prepared by EcoRI digestion of a plasmid (pUL#SB94). Fragments of genomic DNA containing point mutations were amplified by PCR using the original purified fosmid as the template. The forward primer consisted of the same 50 nucleotide HA used to amplify the RT cassette with the desired mutation directly 3′ of the HA, followed by a further 18–22 nucleotides corresponding to the target. The reverse primer was a short 18–22 nucleotide oligonucleotide corresponding to the 5′ end of the reverse HA used to amplify the RT cassette. Cells were electroporated with the appropriate DNA, purified using a QIAquick Gel Extraction Kit (Qiagen), with selection for streptomycin resistance to detect the loss of the RT cassette. Potential positive clones were re-streaked and PCR screened. When using the EL350 strain, DNA was extracted and electroporated into the Copy Control strain EPI300. (MW005 contains both Red functions and Copy Control capability, and so transfer to EPI300 is then not necessary). Fosmid DNA was prepared and integrity confirmed by restriction enzyme digestion and/or sequencing. All primers were synthesized by IDT and long primers were PAGE-purified.
Recombineering-mediated fosmid ‘stitching’
Recombineering was used to generate single fosmids, containing the whole of daf-16 or nurf-1, from pairs of overlapping fosmids, each partially covering the gene, WRM0610bB12 and WRM065dE01 for daf-16, WRM0629dF11 and WRM0610dH04 for nurf-1. The recombineering technology was as described above but following the scheme presented in Additional file 4. An RT cassette was recombineered into the first fosmid named for each gene, within the region of overlap between the fosmids, for subsequent replacement with the second half of the gene from the second fosmid, in the second recombineering step. For daf-16, the inserts in both fosmids were in the same orientation with respect to the vector backbone, simplifying the manipulations. Due to the reverse orientation of the inserts for nurf-1, the RT cassette was generated by two PCR reactions to add in a 50 bp region corresponding to the end of the insert in the second fosmid. This then allowed the second half of nurf-1 to be introduced into the first fosmid by recombineering. To address the reduced efficiency of recombineering with large fragments, a kanamycin cassette, amplified by PCR using primers with appropriate homology arms and pENTR201 (Invitrogen) as template, was inserted downstream of the target gene segments in the second fosmid, again by recombineering, selecting directly for kanamycin resistance. Fosmid DNAs containing the inserted kanamycin cassette were prepared and digested by restriction enzymes to release the target gene segments, SbfI and AfiII for daf-16 and SmaI for nurf-1. The gene segments were purified using the Qiaex II Gel Extraction Kit (Qiagen) for use in the second recombineering step. Replacement of the RT cassette with the downstream gene segment was selected for with kanamycin resistance. Potential clones were screened by PCR and the integrity of the resulting fosmids was confirmed by restriction enzyme digestion.
C. elegansculture and transformation
C. elegans strains were maintained as previously described . The wild type Bristol N2 strain  was transformed by microinjection  with fosmid DNA at 5–20 ng/ml and pRF4 plasmid DNA at 100 ng/ml. pRF4 contains rol-6(su1006), conferring a rolling phenotype, allowing detection of transformants and maintenance of transgenic lines. The extrachromosomal arrays created in the transformation events typically contain both plasmid and fosmid DNA. Each transgenic line was derived from a different microinjected animal to ensure independence. GFP expression patterns were observed by epifluorescence microscopy with Chroma Technology Corp. filter set 41012 or Zeiss filter set 47 on a Zeiss axioplan microscope or on a Leica DMR microscope, respectively, equipped with DIC optics. Images were collected with a Photometrics CoolSNAP camera and Improvision Openlab software.
This research was supported by Wellcome Trust Grant 082603/B/07/Z and BBSRC grant BB/E008038/1.
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