Comprehensive analyses of the BES1 gene family in Brassica napus and examination of their evolutionary pattern in representative species

Background The BES1 gene family, an important class of plant-specific transcription factors, play key roles in the BR signal pathway in plants, regulating various development processes. Until now, there has been no comprehensive analysis of the BES1 gene family in Brassica napus, and a cross-genome exploration of their origin, copy number changes, and functional innovation in plants was also not available. Results We identified 28 BES1 genes in B. napus from its two subgenomes (AA and CC). We found that 71.43% of them were duplicated in the tetraploidization, and their gene expression showed a prominent subgenome bias in the roots. Additionally, we identified 104 BES1 genes in another 18 representative angiosperms and performed a comparative analysis with B. napus, including evolutionary trajectory, gene duplication, positive selection, and expression pattern. Exploiting the available genome datasets, we performed a large-scale analysis across plants and algae suggested that the BES1 gene family could have originated from group F, expanding to form other groups (A to E) by duplicating or alternatively deleting some domains. We detected an additional domain containing M4 to M8 in exclusively groups F1 and F2. We found evidence that whole-genome duplication (WGD) contributed the most to the expansion of this gene family among examined dicots, while dispersed duplication contributed the most to expansion in certain monocots. Moreover, we inferred that positive selection might have occurred on major phylogenetic nodes during the evolution of plants. Conclusions Grossly, a cross-genome comparative analysis of the BES1 genes in B. napus and other species sheds light on understanding its copy number expansion, natural selection, and functional innovation. Electronic supplementary material The online version of this article (10.1186/s12864-018-4744-4) contains supplementary material, which is available to authorized users.

The BES1 gene family plays key roles in the BR signalling pathway. BES1 binds to the promoter region of SAUR-AC1, which has become a molecular tool to dissect brassinosteroid and auxin responses [2,10]. In addition, BES1 interacts with a bHLH protein BIM1 (BES1-interacting Myc-like1) to synergistically bind to E-box sequences that are present in many BR-induced gene promoters [2,11]. In A. thaliana, several members of the BES1 gene family have been identified, such as BES1, BZR1, and BEH1-4. These transcription factors have a gene function that is redundant in the BR signalling pathway [2]. The BES1 genes contain an NLS (Nuclear localization signal), followed by a highly conserved amino-terminal domain (N), phosphorylation domain (P), a PEST motif, and a carboxyl-terminal domain (C). The central P domain of BES1 genes is the target of BIN2 kinase, and the PEST motif is implicated in protein degradation [2,12].
There are few prior studies on the evolution of the BES1 gene family. Recent studies have found that the BES1 locus in A. thaliana encodes two isoforms, long and short BES1 (BES1-L and BES1-S). Among them, BES1-L has an additional 22 amino acids in the N terminal, and it has a stronger biological function than BES1-S. It can promote the nuclear localization of BZR1 and BES1-S [13]. BES1-L is an important isoform in the BR signalling pathway, and it uniquely exists in the majority of A. thaliana ecotypes. BES1-L is a more recently evolved isoform and may have contributed to the expansion and evolution of A. thaliana [13]. BES1 shows relaxed selection compared to BZR1, hallmark of suband neofunctionalization, and dynamic HSP90 client status across independent evolutionary paths [14]. By ChIP-chip and gene expression analyses, a comprehensive transcriptional network for BES1-regulated genes was constructed, which contained 1609 putative BES1 target genes [15]. For a member of the BES1 gene family, the phylogenetic tree indicates that angiosperm BZR1like genes form two groups, BZR1 and BZR2/3/4. However, only one BZR1-like gene was detected in the basal extant angiosperm (A. trichopoda). These two groups may be generated by a gene duplication event before the diversification of extant angiosperms, while A. trichopoda lost the BZR1 member during its evolution [16]. Previously, we also conducted a genome-wide analysis of the BES1 gene family in Chinese cabbage, and explored its structural and functional changes in the process of evolution [17].
In that it is pivotal in its importance to plant growth, the BES1 gene family has been identified and analysed in some plants, including A. thaliana [2], O. sativa [18], and B. rapa [17]. However, in B. napus, there is a lack of studies on the function and structure of the evolution of the BES1 gene family. B. napus is an important oilseed crop grown worldwide as a member of the genus Brassica. B. napus (AACC genome), an allopolyploid, originated from hybridization of B. rapa (AA genome) and B. oleracea (CC genome) [19]. The availability of these Brassica genomes, together with those of a model species, provided an opportunity to understand the formation and evolution of the BES1 gene family.
The aims of this study were to: (i) identify and characterize the BES1 gene family in B. napus and 18 other species to understand their evolutionary pattern across plant species; (ii) to characterize their phylogenetic relationships, origin and evolution, and infer duplicated genes; (iii) by inferring gene collinearity, to find how polyploidization has contributed to the evolution of this gene family; and (iv) to explore expression patterns of BES1 genes in two tissues based on the transcriptome and microarray data. This comprehensive analyses contributes to our understanding of the functional innovation of this important gene family, as well as the effect of gene loss, retention, and expansion, especially due to recursive polyploidization.

Retrieval of genome sequences
The B. napus and 18 representative genome sequences were used for comparative analyses. These species contained 6 dicots, 5 monocots, 1 basal angiosperm, 1 Pteridophyta, 1 Bryophyta, and 5 green algae (Fig. 1). The genome sequences of B. napus were downloaded from the Genoscope genome database [19]. The A. thaliana sequences were downloaded from TAIR, and the rice sequences were downloaded from RGAP [20]. The B. rapa sequences were from BRAD [21] and the B. oleracea sequences were from EMBL (http://www.ebi.ac.uk/). The A. trichopoda sequences were downloaded from the Amborella Genome Database [22]. The sequences of the other species were downloaded from phytozome [23].
Identification and characterization of the BES1 gene family.
The Pfam database (version 31.0) was used to identify BES1 genes from all protein sequences with a threshold of e-value <1e-5 [24]. BES1 genes have the typical BES1_ N domain (PF05687.9). The retrieved BES1 candidates were further verified by using the SMART and Conserved Domain Database with default parameters [25,26]. To eliminate possible pseudogenes, sequences with < 150 amino acids were removed for further analysis. MEME (version 4.12.0) was used to search for conserved motifs, and the number of motifs was set as 10 [27]. The protein structure was predicted using the Swiss-model database [28]. The interaction networks of A. thaliana BES1 genes were constructed using the STRING database (http://string-db.org). The RNA-seq data was used to analyse BES1 gene expression in leaves and roots in B. napus [19]. This dataset contained three replicates, and the RPKM value was log10 transformed. Expression data of A. thaliana genes were obtained from the BAR database (http://bar.utoronto.ca/) [29,30]. The expression analysis of BES1 genes under heat, cold and salt treatments by qRT-PCR was conducted according to our previously reported methods [31,32].

Sequence alignment and phylogenetic analyses
Multiple sequence alignment was performed using MUSCLE with default parameters [33]. Based on alignment, we generated a phylogeny using previously reported methods [34]. Phylogenetic analyses were conducted using three methods: Neighbour-joining (NJ), Maximum Likelihood (ML), and Bayesian. NJ trees were constructed using MEGA 6.0 with 1000 bootstrap and a Poisson correction model [35]. The MrBayes v3.2.6 software was employed to construct Bayesian trees using the fixed (Jones) model for amino acid substitutions that was run for 4 × 10 6 generations, with 6 Markov chains, sampled every 1 × 10 4 generations [36]. PhyML 3.0 was employed to construct ML trees, with the Jones, Taylor and Thorton (JTT) model, and 100 nonparametric bootstrap replicates [37]. The reconstructed BES1 gene trees were compared with real species trees by lineage using Notung 2.9 software with default parameters [38].

Orthologs, paralogs, duplicated type, and collinear blocks identification
Orthologous and paralogous BES1 genes were identified using OrthoMCl (v2.0, e-value: 1e-5), and then we counted the orthologous gene pairs for each A. thaliana BES1 gene manually [39]. Their relationships were constructed using Cytoscape (v3.6.0) [40]. First, wholegenome protein sequences from all species were searched against themselves using BLASTP with an Evalue of 1 × 10 − 5 . MCScanX v1.0 (−k 50, −s 5, −m 25) was then used to detect the duplicated type and collinear blocks according to a previous report [41]. Then, we extracted the BES1 genes located in the collinear blocks by Perl scripts.

Selective pressure detection in each group
To estimate the divergence time between collinear BES1 gene pairs, alignment of protein sequences was performed using ClustalW2.0, and then translated into CDS alignment. We applied likelihood ratio tests of positive selection based on ML methods and codon substitution models. Based on reported methods [42,43], to find evolutionary traces of selective pressures, we analysed each group to infer ω (the ratio of nonsynonymous to synonymous distances) using Codeml implemented from PAML4.9 [44,45]. We employed a complete deletion method when analysing alignments with gaps, and eliminated sequences that contained 40% of their length or more as InDels. We detected variation in ω among sites by employing a likelihood ratio test between the M0 and M1 and M7 and M8 models.

Identification and characterization of the BES1 gene family
We systematically identified BES1 genes by searching Pfam database in B. napus and 18 other representative species, including 5 dicots (B. rapa, B. oleracea, A. thaliana, A. lyrata, and C. rubella), 5 monocots (S. bicolor, Z. mays, S. italica, O. sativa, and B. distachyon), 1 basal angiosperm (A. trichopoda), 1 Pteridophyta (S. moellendorffii), 1 Bryophyta (P. patens), and 5 green algae species (Fig. 1). After filters, a total of 132 BES1 genes were identified among all species. Allotetraploid plant B. napus contained the most BES1 genes (28), being just the addition of its two diploid progenitors B. rapa (15) and B. oleracea (13) (Fig. 1). Generally, there were more BES1 genes in diploid Brassica genomes than others due to their shared genome duplication event. No BES1 gene was identified in the five green algae species. This result indicated that the BES1 genes were subjected to largescale expansion in higher plants.

Phylogenetic and classification analysis of BES1 genes
To conduct the classification of BES1 genes, we constructed a phylogenetic tree using all of the examined species by MEGA 6.0. The 132 BES1 genes of the 14 species were clearly grouped into six groups (A to F) according to the bootstrap values and phylogenetic topology (Fig. 2a). Furthermore, groups A and B were divided into 2 distinct subgroups (A1 and A2, B1 and B2), respectively. The group F was further divided into 3 subgroups corresponding to F1 to F3. In P. patens and S. moellendorffii, all BES1 genes were assigned into C, E, and F3 groups (Figs 1, 2a). However, there was no BES1 gene detected in group C among the angiosperm species, indicating that the genes of group C might have experienced an evolutionary divergence in structure or function.
Among B. napus and other 5 dicots, we found that more than 70% of genes belonged to groups A and B, and there was no BES1 gene in groups C, D, E, and F3 ( Fig. 1). Furthermore, the results showed that the expansion of BES1 genes in 3 Brassica species mainly occurred in groups A and B due to their genome duplication events. In the 5 monocots species, there was no gene in groups A2, B2, C, and F3 ( Fig. 1). Interestingly, we found that groups D and E contained BES1 genes in most of the monocots but not in the dicots. In addition, we noted that S. bicolor, Z. mays, and S. italica contained 3 genes in group D, while there was no gene in this group for O. sativa and B. distachyon. These results indicated that there have been lineage-specific expansion of BES1 genes after the divergence of dicots and monocots.

Positive selection analyses for the BES1 gene family
Strong positive selection was observed for the major nodes on the phylogenetic tree, which possibly contributed to the divergence of higher plants. To uncover whether and when natural selection had acted on the evolution of the BES1 gene family, we performed selection pressure analyses in each group using PAML program. Taking the F1 group as an example, 1 significantly nonsynonymous vs synonymous substitution (ω = 999.00, 2Δl = 61.92) was detected, showing a strong positive selection after the divergence of Brassica and other species (Fig. 2b). This branch contained 4 Brassica genes, such as Bol-BES1-004, Bna-BES1-019, Bra-BES1-012, and Bna-BES1-004.
Furthermore, we also detected positive selection for other groups (Additional file 1: Figure S1). The results showed that there were more positive selection nodes in groups A1, B1, and D than in the other groups, and the number reached 3 (Fig. 2c). In groups A2, B2, and E, 2 positive selection nodes were detected, and there was no positive selection node in group C. Generally, we found there were more positive selection nodes in dicots (12, groups A, B, F1, and F2), followed by monocots (5, groups D and E). This result indicated that BES1 genes in dicots underwent more positive selection than those in other lineages.

Conserved motif analysis of BES1 genes exploring their origin and evolutionary pattern
To further explore the origin and evolutionary pattern of BES1 genes, the most conserved 10 motifs (M) were detected by MEME program (Fig. 3a, Additional file 2: Figure S2). The M1 was located at the amino-terminal domain (N), and M2, M8, and M9 constituted BIN2 phosphorylation sites (P), and M3, M10 belonged to the carboxyl domain (C) (Fig. 3b). All genes had M1 and M2, while the other 8 motifs existed in some but not all groups (Additional file 2: Figure S3).
We found specific preservation and expansion of motifs in different plant lineages (Fig. 3c). Among F subgroups, F3 contained 5 genes, including 2 P. patens, 2 S. moellendorffii, and 1 A. trichopoda genes, while subgroups F1 and F2 only contained angiosperm genes. Interestingly, we found subgroups F1 and F2 contained M4 to M7, which were absent in F3 and other groups. For group E, only M1 and M2 were detected, and this group did not contain dicot genes. For group C, M1, M2, and M9 were identified, which only contained 2 P. patens, and 2 S. moellendorffii genes. Group D was specific for monocots, and contained M1, M2, M9, and M10, while M9 might have lost some genes. Two main groups, A and B, existed in most angiosperm species. Most genes in these two groups contained M1, M2, M8, M9, M3, and M10.
For genes in groups F1 and F2, we detected an additional domain, glyco_hydro_14, being contained in M4 to M8 (Additional file 2: Figure S3). To explore the sequence divergence of BES1 genes among F1, F2 and F3, we conducted sequence alignments using all genes belonging to the F group (Additional file 2: Figure S4).
The results showed that the first 70 amino acids of the BES1_N domain were very conserved among the three subgroups. We found 12, 36, 40, and 45 amino acids in the BES1_N domain were the same in the F1 and F2 subgroups, which were different from the F3 subgroup. For the Glyco_hydro_14 domain, we found that it was conserved between the F1 and F2 subgroups, while it was divergent or had lost parts in the F3 subgroup (Additional file 2: Figure S4). We further conducted protein structure analyses using the Swiss-model database. We found that its homology model was 1fa2.1.A, with a similarity of up to 46.59% (Additional file 2: Figure S5a). Further assessment also showed that this predicted model had high quality and accuracy (Additional file 2: Figure S5b-d).
Identification of orthologous and paralogous BES1 genes between B. napus and other species.
We identified orthologous gene pairs between B. napus, A. thaliana, O. sativa, A. trichopoda, S. moellendorffii, P. patens and other species, respectively using the OrthoMCL program (Additional file 3: Table S1). There were more orthologous pairs between B. napus and B. oleracea (32), followed by B. rapa (29) and A. thaliana (23) (Fig. 4a). Taking the orthologous genes between A. thaliana and other species as an example, we constructed an interaction network (Fig. 4b). There were more orthologous gene pairs for Ath-BES1, Ath-BZR1, Ath-BAM7, Ath-BEH3, and Ath-BMY2 in A. thaliana versus B. napus than versus others (Fig. 4c). For Ath-BEH2, only one orthologous gene pair was identified for A. thaliana versus each Brassica species, while there was no orthologous gene between A. thaliana and others. In O. sativa, there were more orthologous genes between O. sativa and monocots than other comparisons (Additional file 2: Figure S6a). For Osa-BES1-003, 4 orthologous gene pairs were detected between O. sativa and B. napus, which was more than for other comparisons (Additional file 2: Figure S6b). Furthermore, orthologous gene pairs were also detected between A. trichopoda, S. moellendorffii, P. patens, and other species (Additional file 2: Figure S7-9).
Whole-genome duplication (WGD) may have contributed to the expansion of the gene family. Additionally, 15 paralogous BES1 gene pairs were identified in B. napus, which was far more than in A. thaliana and other plants (Additional file 2: Figure S10, Additional file 3: Additional file 3: Table S2). This might be a result of additional WGDs after its split from A. thaliana. In addition, we found that 4 BES1 genes in B. napus had more than 1 paralogous gene, including Bna-BES1-007, Bna-BES1-004, Bna-BES1-019, and Bna-BES1-020 (Additional file 3: Figure S10). In A. trichopoda, there were no paralogous BES1 genes. Therefore, the number of paralogous information could partly reflect species genome duplication.

Duplicated type identification and synteny analyses of B. napus and other species
Various gene duplications may have contributed to the expansion of the gene family. We found evidence that WGD likely contributed the most to the expansion of this gene family in many plant lineages. We examined 5 types of gene duplications: singleton, dispersed, proximal, tandem, and WGD or segmental duplication by MCScanX program (  The correspondence relationship between schematic structures of BES1 and motifs. c The major evolutionary trajectories of the BES1 gene family. The white X indicated the motif was lost in some genes monocots, the dispersed duplication contributed the most to gene expansion. For A. trichopoda and S. moellendorffii, all BES1 genes belonged to the dispersed duplication. Actually, by checking gene collinearity within a genome, we found that more than 55.0% of BES1 genes in B. napus and the other 5 dicots were located in collinear blocks, showing their duplication during polyploidization (Additional file 3: Table S4). Especially for the 3 Brassica species, more than 75% of BES1 genes were located in collinear blocks. A percentage of 37.5, 37.5, and 33.3% of BES1 genes were located in collinear blocks for S. bicolor, Z. mays, and S. italica, respectively. Furthermore, we found that the percentage of BES1 genes located in the collinear blocks was larger than the average genome-wide level for all examined species except A. trichopoda and S. moellendorffii (Additional file 3: Table S4). The percentage for BES1 genes in colinearity was significantly larger than the average genome-wide level by χ 2 test, and P-values were 6.69E-18 and 1.21E-17 for dicots and monocots, respectively.

Differential BES1 gene losses and duplications during evolution
Expansion of BES1 genes in WGDs was also accompanied by gene losses. To clarify the evolution of the BES1 gene family, we conducted the gene loss and duplication analyses using Notung [46]. We obtained  Figure S11). In the lineage leading to the common ancestor of P. patens, S. moellendorffii, and angiosperms, 8 ancestral genes were duplicated, which occurred 439 Mya, while no gene was lost. In the lineage of the common ancestor for A. trichopoda and angiosperms, 2 ancestral genes were duplicated, and 3 genes were lost, which occurred during the Jurassic period. In the lineage leading to the common ancestor of dicots and monocots, 2 ancestral BES1 genes were duplicated and lost, respectively (Fig. 5a). For the branch of the common ancestor of B. napus and 5 dicots, 8 ancestral genes were duplicated, and 2 genes were lost. Since the divergence, the A. thaliana lineage lost 2 genes and there were no duplications. For 3 Brassica species, 15 ancestral genes were duplicated, and 3 genes were lost in the branch of their common ancestor. The B. oleracea and B. rapa lineage  The duplication or losses analyses of BES1 genes in A. thaliana and 3 Brassica species lost 11 and 10 genes, respectively, and no duplicated genes were detected. However, the B. napus lineage had no gene losses, and only 1 duplicated gene was detected.
For the 5 monocots, 5 ancestral BES1 genes were duplicated, and 2 genes were lost in their lineage of the common ancestor (Fig. 5a). In the common ancestor of O. sativa and B. distachyon, 2 ancestral genes were lost, and no ancestral gene was duplicated. Since the divergence, each of the B. distachyon and O. sativa lineages lost 3 genes, and there was no duplicated gene. In the common ancestor of Z. mays, S. bicolor, and S. italica, 3 ancestral genes were lost, and 2 ancestral genes were duplicated. In conclusion, there were more BES1 gene losses than duplications. The ratio of losses and duplications was 28 versus 2 in dicots, and this ratio was 16 versus 3 in monocots. These results will help us to understand the loss, retention and expansion of this gene family during the evolution of different species.
Exploring BES1 gene function in B. napus by comparing it with A. thaliana A comparison of sequence homologs between nonmodel and model species might aid in understanding the function of these BES1 genes in non-model species. Taking 3 Brassica species as an example, we constructed three phylogenetic trees for these species and A. thaliana. On the phylogenetic tree, 8 groups (G1 to G8) were obtained according to the BES1 genes of A. thaliana (Fig. 5b). There was no gene loss in G1, while there were 2 or 4 gene losses in the other 7 groups. The BES1 genes within the same taxonomic group with A. thaliana might have similar functions. Therefore, we conducted comprehensive analyses to further explore the function of BES1 genes. First, we constructed interaction networks between each BES1 gene and their corresponding target genes to uncover their regulatory pathways (Fig. 6, Additional file 3: Tables S5, S6). Most target genes were identified in the networks of Ath-BES1, Ath-ZR1, Ath-BEH4, and Ath-BMY2, and the number of target genes achieved 10. Among all eight groups, there were the most B. napus genes involved in Ath-BES1 networks. Interestingly, we identified 4 target genes (BRI1, BSU1, BIN2, and DWF4), which were involved in BES1 and BZR1 networks (Fig. 6). Furthermore, we conducted enrichment analyses for the genes involved in these networks, and found that most genes responded to the brassinosteroid signalling pathway (Additional file 3: Table S7).

Comparative expression pattern analysis of BES1 genes between A. thaliana and B. napus
To detect the functional divergence of BES1 genes, their expression was compared in different tissues, i.e., roots and leaves, between A. thaliana (Additional file 3: Table  S8) and B. napus (Fig. 7, Additional file 3: Table S9). The results showed that Ath-BEH1 had high expression (log2 (ratio) > 1.5) in leaves, whereas it showed low expression in roots. Four genes (Ath-BEH4, Ath-BEH3, Ath-BAM7, Ath-BMY2) were expressed at low levels in leaves (log2 (ratio) < 0). In roots, 3 of 8 genes showed high expression, including Ath-BAM7, Ath-BEH3, and Ath-BEH2. For B. napus, we found that several genes showed high expression in both leaves and roots, such as all 4 genes in group 4 (G4) and four genes in G1 (Bna-BES1-008,009,012, 026). Interestingly, we found there was similar expression of these genes in the same group between A. thaliana and B. napus. For example, the expression of Bna-BES1-005, and Bna-BES1-025 (G3) had similar patterns to Ath-BEH1 in both roots and leaves. However, Bna-BES1-028 and Bna-BES1-010 were also located in G3, but their expression pattern was significantly different from Ath-BEH1 (Fig. 7a). This might be due to the possibility of subfunctionalization or neofunctionalization after the divergence of A. thaliana and B. napus. In addition, we also found that the expression level of almost all genes in subgenome A was higher than that of subgenome C in roots (Fig. 8, Additional file 2: Figure S12). Furthermore, we collected and analysed the expression of BES1 genes in model species, which could be helpful for our understanding of homologous gene function in non-model species. Take the BES1 gene as an example, we investigated its expression pattern in A. thaliana under different stresses, such as cold, heat, and salt (Fig. 7b). To explore the expression pattern of the duplicated genes, we conducted the qRT-PCR analyses for BES1 genes in B. napus under cold, heat, and salt treatments. Among the G1 group, there were 6 duplicated genes in B. napus with the A. thaliana BES1 gene. The results showed that Bna-BES1-013 had a relatively low expression (Fig. 7b). This indicates that not all duplicated genes are highly expressed, and some genes may be de-functionalized after duplication.

Discussion
Origination, evolution and expansion of BES1 family genes The evolution and origin of BES1 genes in representative plants were analysed, and their evolutionary pattern was determined using phylogenetic and conversed motif analyses. As to our phylogenetic analysis, BES1 family genes may have first originated from the group F3, which contains only the M1 and M2 motifs. Then, it developed novel genes through acquiring other motifs, such as M2 to M10. Furthermore, several specific groups or subgroups were obtained for dicot and monocot species. In groups F1 and F2, we detected an additional domain contained M4 to M8, which did not exist in the other groups. The WGD or segmental duplication contributed the most to the expansion of this gene family among all 6 dicots [47,48]. However, the dispersed duplication contributed the most to its expansion in 3 monocots. The percentage of BES1 genes located in collinear blocks was significant larger than the average genome-wide level for nearly all examined species.
The Brassica genome has undergone genome duplication events since its divergence from A. thaliana [47,[49][50][51]. Furthermore, B. napus, an allopolyploid, originated by hybridization between B. rapa and B. oleracea only7 500 years ago [19]. Therefore, the A. thaliana gene should have 3 corresponding B. oleracea and B. rapa genes and have 6 B. napus genes if no gene was lost. However, there is a high possibility of gene loss after WGD events. For all 7 A. thaliana BES1 genes except Ath-BES1, the loss events occurred in B. rapa and B. oleracea (Fig. 5b). On inspection, B. napus BES1 genes were lost when comparing with A. thaliana genes. In fact, we thought the BES1 gene was not lost, because B. napus originated by hybridization of B. rapa and B. oleracea, and the loss occurred during the fusion of these two genomes.

BES1 gene expression pattern and network construction in B. napus and model species
The BR signalling pathway has been studied thoroughly at the genetic and molecular level in A. thaliana [52][53][54]. The studies showed that BZR1 and BES1 are important components of BR signal transduction [55,56]. Plants with impaired BR production exhibit many growth defects, such as dwarfism, or organ expansion reduction [57,58]. BES1 genes repress the expression of several BR biosynthesis enzymes, such as CPD and DWARF4 [59,60]. Based on the microarray and ChIP-chip data, 1609 and 953 BR-regulated target genes have been identified for BES1 and BZR1, respectively [15,61]. The construction of an expression detection or interaction network will aid in revealing the regulation of BES1 genes.
In this study, we conducted expression analyses of BES1 genes in B. napus and A. thaliana by using RNA-Seq and qRT-PCR datasets. In B. napus, most genes of the G1 and G4 groups showed higher expression in both roots and leaves. Interestingly, we found that not all duplicated genes were highly expressed. In the G1 group, there were 4 and 2 homologous genes with the A. thaliana BES1 gene in subgenome A and C, respectively. However, the Bna-BES1-013 (from subgenome A) and Bna-BES1-027 (from subgenome C) had a lower expression level than the other 4 genes in roots and leaves. Similarly, this phenomenon was also found under cold, heat, and salt treatments. The results indicated that some genes may be sub-, neo-or defunctionalized during the species' evolution. Furthermore, we conducted interaction networks for B. napus and A. thaliana. The network was more complex for BES1, BZR1, and BEH1 than for other genes. This indicated that they may play a more important core role in the regulation network. Comparative analysis of the expression pattern and construction of the regulatory network will provide a very favourable support for the study of BES1 gene function in B. napus and other related species.
Exploring BES1 gene function in non-model species The functions of most BES1 genes have been well characterized in A. thaliana. BES1 targets are not only auxin responsive genes, but are also auxin efflux facilitators (PIN4, PIN7), which have profound effects on auxin action [15,62]. Based on microarray and chromatin immune precipitation (ChIP), AtMYB30 was identified, which is a direct target gene of AtBES1 [63]. By spectrometry identification and genetic analysis, it was found that MAX2 mediates the ubiquitination and degradation of BES1 protein [64]. In addition, the BES1 gene is a direct substrate for MPK6 to regulate the immune response of plants [65]. BZR1 mediates a trade-off between plant innate immunity and growth [66]. Therefore, a comparison of sequence homologs between model and non-model species might aid in understanding the function of these BES1 genes in non-model species. Taking the Brassicaceae species as an example, we checked genes within the same taxonomic group on the phylogenetic tree, which could have similar functions (Fig. 5b).

Conclusions
In conclusion, we comprehensively analysed the evolutionary pattern, gene synteny, gene duplication or losses, orthologous and paralogous genes, positive selection, and interaction networks of BES1 genes involved in the BRs pathway. A total of 132 BES1 genes were identified among 19 representative species. This effort can serve as a first step in comprehensive functional characterization of BES1 genes by reverse genetic approaches and molecular genetics research. This study provides useful resources for future studies on the structure and function of BES1 and for identifying and characterizing these genes in other species. In addition, this study may also facilitate our understanding of the effect of duplication or losses during the evolution of polyploidy.

Additional files
Additional file 1: Figure S1. The positive selection analyses for each group of BES1 gene family in representative species. The ω on the clades is dn/ds value under M8 model of codeml, which indicates the positive selection nodes. (PDF 634 kb) Additional file 2: Figure S2. The sequences of motif 1 to motif 10 of BES1 gene family among examined species. Figure S3. The conversed motifs (M1 to M10) analyses for each group using the MEME program. Figure S4. The sequences alignment of F1, F2, and F3 subgroups among examined species. The Glyco_hydro_14 domain contained in F1 and F2 subgroups is marked using the blue dashed box in F3 subgroup. Figure  S5. The analyses of Glyco_hydro_14 domain, including (a) protein structure, (b) alignment with the homology model (1fa2.1.A), (c) prediction of local similarity to target, (d) comparison with non-redundant set of PDB structures. Figure S6. The analyses of orthologous BES1 genes between O. sativa and other examined species. (a) The interaction network constructed using the orthologous gene pairs between O. sativa and other species. (b) The number of orthologous genes in each species with 6 O. sativa BES1 genes. Figure S7. The analyses of orthologous BES1 genes between A. trichopoda and other examined species. (a) The interaction network constructed using the orthologous gene pairs between A. trichopoda and other species. (b) The number of orthologous genes in each species with 4 A. trichopoda BES1 genes. Figure S8. The analyses of orthologous BES1 genes between S. moellendorffii and other examined species. (a) The interaction network constructed using the orthologous gene pairs between S. moellendorffii and other species. (b) The number of orthologous genes in each species with 4 S. moellendorffii BES1 genes. Figure  S9. The analyses of orthologous BES1 genes between P. patens and other examined species. (a) The interaction network constructed using the orthologous gene pairs between P. patens and other species. (b) The number of orthologous genes in each species with 6 P. patens BES1 genes. Figure S10. The analyses of paralogous BES1 genes in each of the examined species. The green lines indicated the 4 B. napus BES1 genes, which had more than 1 paralogous genes. Figure S11. The reconstructed phylogenetic tree according to the duplication and losses of BES1 genes at different stages of plant evolution. Figure S12. The histogram of BES1 genes expression in root and leaf of B. napus. The genes marked with green located subgenome A, and red located subgenome C of B. napus. (PDF 4242 kb) Additional file 3: Table S1. The list of orthologous BES1 gene pairs between B. napus, A. thaliana, O. sativa, A. trichopoda, S. moellendorffii, P. patens and other examined species. Table S2. The list of paralogous BES1 gene pairs in each of other examined species. Table S3. The duplicated type of BES1 genes in B. napus and each representative species. Table S4. The comparative of synteny analyses for BES1 genes and all genes in B. napus and other representative species . Table S5. The domain and annotation of the BES1 genes and their target genes in A. thaliana network for comparative ananlysis with B. napus. Table S6. The nodes information and the assessment of the interaction network for BES1 genes in A. thaliana. Table S7. The enrichment ananlyses of the genes involved in the BES1 genes networks in A. thaliana for comparative ananlysis with B. napus. Table S8. The expression information of the BES1 genes in root and leaf for A. thaliana, and the gene expression was obtained from the BAR database. Table  Availability of data and materials All data generated or analysed during this study were included in this published article and the Additional files.