Genomic characterization of the European sea bass Dicentrarchus labrax reveals the presence of a novel uncoupling protein (UCP) gene family member in the teleost fish lineage
© Tine et al.; licensee BioMed Central Ltd. 2012
Received: 8 October 2011
Accepted: 11 May 2012
Published: 11 May 2012
Uncoupling proteins (UCP) are evolutionary conserved mitochondrial carriers that control energy metabolism and therefore play important roles in several physiological processes such as thermogenesis, regulation of reactive oxygen species (ROS), growth control, lipid metabolism and regulation of insulin secretion. Despite their importance in various physiological processes, their molecular function remains controversial. The evolution and phylogenetic distribution may assist to identify their general biological function and structure-function relationships. The exact number of uncoupling protein genes in the fish genome and their evolution is unresolved.
Here we report the first characterisation of UCP gene family members in sea bass, Dicentrarchus labrax, and then retrace the evolution of the protein family in vertebrates. Four UCP genes that are shared by five other fish species were identified in sea bass genome. Phylogenetic reconstitution among vertebrate species and synteny analysis revealed that UCP1, UCP2 and UCP3 evolved from duplication events that occurred in the common ancestor of vertebrates, whereas the novel fourth UCP originated specifically in the teleost lineage. Functional divergence analysis among teleost species revealed specific amino acid positions that have been subjected to altered functional constraints after duplications.
This work provides the first unambiguous evidence for the presence of a fourth UCP gene in teleost fish genome and brings new insights into the evolutionary history of the gene family. Our results suggest functional divergence among paralogues which might result from long-term and differential selective pressures, and therefore, provide the indication that UCP genes may have diverse physiological functions in teleost fishes. Further experimental analysis of the critical amino acids identified here may provide valuable information on the physiological functions of UCP genes.
Gene duplication via single gene, larger-scale fragment or whole genome duplication is known as a major evolutionary force for creating new genes [1–3]. While the “parental” copy conserves its original function, duplicated genes may undergo functional diversification by evolving new functions and therefore offer the organisms the ability to adapt to new environmental conditions [4–8]. Duplicated genes are hierarchically gathered in gene families in the genome whose expansion will depend on the number of duplication rounds and the force of selection pressures acting on duplicates resulting in their retention or loss . Unconstrained duplicates may accumulate degenerative mutations and will be therefore eliminated from the genome by purifying selection [10, 11].
Uncoupling proteins (UCP) are evolutionary conserved proteins involved in the coupling mechanism of the electron transport chain to ATP synthesis which is driven by a proton gradient over the mitochondrial inner membrane. The energy harvested from electrons generates a proton gradient that is used to produce ATP or, by influence of UCPs, may be dissipated as heat . Heat production by mammalian UCP1 is crucial for non-shivering thermogenesis and cold-survival of rodents, hibernators and human infants  while the physiological role of the UCP1 orthologue in ectotherms is unclear.
Several UCP1 homologues including UCP2 and UCP3 have been identified from various tissues in vertebrates. UCP2 with a ubiquitous expression pattern has been implicated in multiple functions including the regulation of reactive oxygen species (ROS) [14, 15], growth control [16, 17], lipid metabolism [18, 19] and regulation of insulin secretion . UCP3, adjacent to UCP2 in genomes and mainly expressed in the skeletal muscle, is related to oxidative and metabolic processes .
In fishes, three members of the UCP gene family (UCP1, UCP2 and UCP3) have been unequivocally identified in many species including zebrafish (Danio rerio), the puffer fish (Takifugu rubripes), the rainbow trout (Oncorhynchus mykiss) and the gilthead sea bream (Sparus aurata) [22–26]. Recent studies have indicated that zebrafish genome contains more than three UCPs. Hughes and Criscuolo  reported the presence of a fourth gene encoding a UCP protein (UCP4). The same authors further showed that the fourth zebrafish is flanked by the same genes like other vertebrate UCP1, which implies that this latter might be an isoform of UCP1 that resulted from alternative splicing or wrong annotation. Interestingly, the sequence of the fourth zebrafish UCP (present in GeneBank) corresponds exactly to one of the two isoforms predicted as UCP4 in Ensembl genome browser, which has been previously identified as UCP1 orthologue in fish by Jastroch et al. . More recently, Tseng et al.  indicated the presence of a fourth UCP (UCP4: different from that previously reported by Hughes and Criscuolo ) and a fifth UCP gene (UCP5) in zebrafish. While their phylogenetic analyses showed that zebrafish UCP4 and UCP5 are grouped in the same clades than their mammal counterparts, the authors found that these two carriers are distantly related to UCP1-UCP3 and the syntenies around are not conserved across mammals, birds, amphibians and fishes, even within teleost lineage. This indicates that names given in the literature to these genes as members of UCP family could be misleading. Hence, the exact number of uncoupling protein genes in fish genome and the evolutionary history of this protein family remain controversial and should be elucidated. The current availability of five sequenced teleost genomes offers the opportunity of performing a range of comparative and evolutionary analyses that would enable to clarify that question.
The accurate identification of unambiguous orthologue genes across species is a critical step for comparative studies aimed at inferring the molecular function of protein sequences and finding genes that are functionally related [29, 30]. The traditional approaches used to establish orthology relationships of gene families are mainly based on constructing multiple alignments of sequences identified by reciprocal best BLAST hits between multiple genomes, which are then used to infer phylogenetic relationships via maximum likelihood or parsimony methods [31, 32]. Although this revolutionary approach enables an accurate orthology assignment between genes, its reliability can be limited when dealing with complex genomes and large gene families, particularly in vertebrate where many genes are partial or imperfectly annotated due the complexity of gene organisation (coding sequences consisted of several exons alternating with intron sequences). Moreover, the BLAST hit searches often return the closest hits which may not have been evolved from a common ancestral gene . A common complementation of this procedure is using synteny-based methods which exploit synteny information to resolve ambiguous orthology assignment between genes in different species . It is worth noting that this approach has some limitations, especially related to large-scale genomic rearrangements and gain or loss of genes that can shuffle synteny information even between closely related species, but also to the incompleteness of many sequenced genomes that renders the detection of conserved synteny complex and difficult. Although the above mentioned methods appear to be somewhat limited, they benefit from a high degree of complementarity that makes them the most reliable and accurate approaches for orthology assignment when applied in parallel.
Our experimental research focuses on the European sea bass, Dicentrarchus labrax, which is a major marine aquaculture species in the European Union. Sea bass UCPs may provide potential targets to impact metabolism and growth, as studies of mammalian UCPs suggest major roles in energy balance and oxidative stress. To our knowledge, there has not been any report on the molecular characterisation of uncoupling protein genes in the sea bass. In this study, we have characterised four members of the uncoupling protein gene family in sea bass. The genomic structure of these four sea bass UCPs have been determined and their orthologues in the available teleost fish genomes have been identified by similarity and conserved synteny searches. Furthermore, we took advantage to the current availability of a large amount of sequence information in many species to re-annotate and retrace the evolution of UCPs in vertebrates. Our results revealed for the first time a fish-specific duplication of uncoupling protein genes.
Annotation and nomenclature of sea bass UCPs
Exon length of sea bass UCP genes
Identification of UCP orthologues in other teleost species
Listing and genomic location of uncoupling protein sequences used in this study
Sequence identity between sea bass and stickleback UCPs
Identity matrix between UCP genes from sea bass and stickleback
Identification of teleost UCP orthologues in other vertebrates
The search for UCP orthologues in vertebrates enabled their identification in a variety of species including mammalians, reptiles, birds and amphibians. The chromosomal location of UCPs and the protein ID in each species are shown in Table 2. The search for UCP1 ortologues in vertebrates enabled its identification in mammals (Human, Mouse, etc.). In amphibians (Xenopus tropicalis), UCP1 was found. However, no UCP1 orthologue sequence was found in birds and reptiles and the synteny search of the region containing flanking genes in the chicken (Gallus gallus) and the Anole lizard (Anolis carolinensis) did not allow identification of sequences similar to UCP1. UCP2 and UCP3 are present in mammals (Human, Elephant, Crow, Dog, Rat and Mouse) and reptiles (Anole lizard), and are adjacent as previously demonstrated in many reports. As in teleost fishes, they are flanked upstream by the same gene (DNAJB13) but they are bounded in their downstream part by C2CD3 located just before PPME1 (Figure 2). In amphibian genomes, only UCP2 was found and it is flanked by the same genes as reptile and mammalian UCP2/UCP3. The re-annotation of the region bounded by the flanking genes by GENSCAN did not enable prediction of another UCP gene, supporting the results of homology searches. Contrary to amphibians, birds have only UCP3 which flanked by the same genes as amphibian UCP2 (Figure 2). Our re-annotation of the region surrounded by the flanking genes did not allow the prediction of new genes. Our search for teleost UCP orthologues in lamprey allows the identification of one UCP gene only, a sequence that has been characterized UCP2 by Wang et al. . We then searched for UCP orthologues in the lancelet which is considered as the closest living invertebrate relative to vertebrates. This allowed the identification of a UCP-like sequence Accession number: ABR10900 in Branchiostoma belcheri. ClustalW multiple alignments revealed that the lancelet UCP-like sequence was 53%, 55% and 56% identical to sea bass UCP1, UCP2 and UCP3, respectively. Comparisons with all vertebrate UCP sequences revealed that the lancelet UCP-like shares more identity (57.6%) with cow (Bos taurus) UCP3. However, these results are in contradiction with those from the phylogenetic analysis including the UCP-like (results not shown) because the latter indicated that lancelet UCP is closer to vertebrate UCP1.
The ratios of nonsynonymous (dN) to synonymous (dS) substitution (ω = dN/dS) were calculated for each teleost UCP cluster. All pairwise comparisons of teleost orthologues are shown in Additional file 2. The average values of ω were 0.393, 0.469, 0.387 and 0.883 for UCP1, UCP2, UCP3 and UCP3L, respectively. According to ω values estimated from the four UCP sequences, we found that UCP3L has the highest dN/dS ratio (0.883) whereas UCP3 has the lowest ratio (0.387). The ω value of UCP3L is about twice the magnitude of the other UCP members. All UCP genes have a dN/dS ratio < 1 apart from UCP3L whose two pairwise comparisons (Seabass/Medaka and Takifugu/Medaka) showed dN/dS ratios > 1 (see Additional file 2). The global dN/dS ratio estimated using REL analysis showed similar results with higher value for UCP3L (ω = 0.890) compared to UCP1 (ω = 0.159), UCP2 (ω = 0.183) and UCP3 (ω = 0.135). The REL analysis found no positively selected sites for UCP1 and UCP3L. One site was positively selected from the REL analysis for UCP2 (codon 47) and UCP3 (codon 270) with a BF ≥ 50, but they were not confirmed as exhibiting very strong evidence for positive selection (BF ≥ 100). The REL analysis indicated that all UCP1 sites are under strong purifying section. The number of sites identified from REL analysis as being under strong purifying selection (BF ≥ 100) was 168, 112 and 71 for UCP2, UCP3 and UCP3L, respectively.
Type-I (θ I ± standard error, upper right diagonal) and type-II (θ II ± standard error, lower left diagonal) functional divergence between UCP clusters in teleost fishes
0.559 ± 0.126*
0.846 ± 0.123*
0.729 ± 0.126*
0.063 ± 0.046
0.205 ± 0.096*
0.291 ± 0.109*
0.128 ± 0.044
0.016 ± 0.045
0.242 ± 0.121*
0.113 ± 0.057
−0.003 ± 0.060
−0.007 ± 0.058
Moreover, critical amino acid residues that might be responsible for the functional divergence of the UCP family in teleost were predicted by calculating the site-specific profile based on posterior probability analysis. A posterior probability value higher than 0.7 (QI (k) > 0.7) was used as a cutoff to identify potential sites of type-I functional divergence in all pairwise comparisons between UCP clusters. Among 283 sites analysed in all pairwise comparisons, 235 amino acid residues (44 of which with QI (k) > 0.9) were predicted as being responsible for site-specific difference (type-I functional divergence) between UCP1/UCP3 clusters (see Additional file 3). The comparisons of UCP1 with UCP2 and UCP3L allowed the identification of 16 and 224 potential sites of type-I divergence, respectively. For the UCP2/UCP3L and UCP3/UCP3L comparisons, three potential sites that have undergone shifted rates have been identified whereas only one site is predicted to be highly functional divergence-related between UCP3 and UCP3L.
Overall, there was no clear evidence for type-II functional divergence but we did further investigate whether it exists any potential site for type-II functional divergence. We applied a cutoff of QII (k) > 1 for site-specific posterior probabilities. Thus, a total of 46 radical changes were identified between all pairwise comparisons (see Additional file 3). Amongst them, the largest number and highest posterior probability values were found in the comparisons with UCP1 (UCP1/UCP3, UCP1/UCP3L and UCP1/UCP2). Only two potential type-II sites were respectively detected in UCP2/UCP3 comparison. No radical change was found in UCP2/UCP3L and UCP3/UCP3L comparisons.
Five so-called UCP homologues UCP1-UCP5 annotated in mammals have been reported in the zebrafish, Danio rerio. While zebrafish UCP1-UCP3 are closely related, UCP4 and UCP5 do not group into the core UCP family . Accordingly, Nedergaard and Cannon  had already suggested that these carriers (UCP4 and UCP5) are wrongly annotated as UCP and do not belong to the uncoupling protein family. In this study, we have identified four different UCP genes closely related in the European sea bass D. labrax. Our further analyses revealed these UCP genes are shared by five other fish species, providing evidence for the existence of four unambiguous UCP gene family members in teleost organisms. Similarity searches revealed that teleost UCP1, UCP2 and UCP3 are clearly orthologues to the corresponding UCP genes in the other vertebrates including amphibians, birds, reptiles and mammals. The detailed analysis of conserved synteny of the region harbouring UCP loci confirmed the similarity results. Mammal, reptile, bird and amphibian UCP1 were flanked with the same genes (ELMOD2, upstream and TBC1D9, downstream) like in teleost fishes. The upstream flanking gene of UCP2/UCP3 was the same (DNAJB13) for teleosts and the other vertebrates, but their downstream flanking was different. Mammal, reptile, bird and amphibian UCP2/UCP3 were bounded upstream by C2CD3 located just before PPME1 that flanks teleost UCP2/UCP3, suggesting that C2CD3 has been lost in teleost fishes. The phylogenetic analyses of vertebrate UCP genes also support the similarity results, because they have enabled the unequivocal identification of the orthologues of these three teleost UCPs in a variety of other vertebrate species. The maximum likelihood analysis revealed that teleost UCP2 was monophyletic with UCP2 of other vertebrates including amphibians and reptiles. This monophyletic character together with the high level of sequence identity within vertebrate UCP2, suggests evolutionary conserved functions. This is in good agreement with the virtual zero of its functional branch length (Figure 6A) that indicates this cluster may have maintained a larger component of ancestral function. Likewise, teleost UCP1 was monophyletic with amphibian and mammalian UCP1 as previously reported by many authors [24, 27, 39]. The UCP1 clade is highly divergent from that of other UCP paralogues as evidenced by its longest branch length, which is indicative of strong selective constraints and functional shifts . This interpretation is in good agreement with our functional analyses that indicated large site-specific differences (type-I functional divergence) and higher posterior probability values (type-II functional divergence) in all pairwise comparisons including UCP1. The longer bF of UCP1 in vertebrates also suggests important functional shifts, which are more marked in teleosts. Mammalian, reptile and bird UCP3 are monophyletic, but their monophyly with their teleost orthologues was not resolved. These observations suggest that teleost UCP3 are highly divergent from that of the other vertebrates, divergence that may be due to an accelerated evolutionary rate of UCP3 either in teleost or in other vertebrates. The functional analyses showed a longer functional branch length in the other vertebrates compared to teleost (bF = 0.280 vs. 0. 060; Figure 6B), suggesting a functional shift during the evolution of UCP3.
After divergence, UCP3L may have diverged in function by adopting part of the roles of the original copy or acquiring an entirely new function. Functional divergence can occur after gene duplication via site-specific rate shift (type-I functional divergence) or radical change in amino acid property, which is called type-II functional divergence. In this study, UCP3/UCP3L comparison showed θI value significantly greater than zero and negative θII value, suggesting that these two genes are functionally divergent from each other and that site-specific shift changes in evolutionary rates would have been the main force for such functional divergence. This conclusion is supported by the posterior probability analysis, which did not find any radical change between UCP3 and UCP3L clusters. Furthermore, the high dN/dS ratio of UCP3L indicates that the protein is under few selective constraints and may have therefore evolved new functions. The overall dN/dS ratio of UCP3L is about 1 and at least twice that of UCP3, which can be due either to a relaxation of negative or purifying selection or to an action of diversifying or positive selection. The REL analysis found no positively selected sites for UCP3L among teleost orthologues and the number of negatively selected sites is much lower than that of the other UCP members including UCP3. These results indicate that the higher dN/dS ratios of UCP3L are due to a relaxation of purifying selection rather than positive selection. Such a relaxation of purifying selection can be attributed to a more recent origin of UCP3L, a finding which is consistent with the idea that recent duplicates tolerate more amino-acid substitutions than old duplicates . It has been demonstrated that members of duplicated genes often evolve at different rates after duplication and that the copy (s) of the duplicated gene that evolve faster have higher dN/dS ratios . The results of the functional distance analysis showed relatively long functional branch length (bF = 0.35; Figure 6) for UCP3L, which implies that this duplicate gene may have lost a larger component of ancestral function after duplication. However, further analyses including tissue-specific expression and studies on protein function are needed to determine whether teleost UCP3 and UCP3L share communalities in function.
The comparison of the number of synonymous and nonsynonymous substitutions per site between UCP orthologues revealed that the products of UCP1-3 genes are highly conserved by purifying selection. This strong purifying selection against mutations that result in replacement of amino acids suggests that these UCP genes play crucial roles in teleost fishes. The examination of site-specific selection pressures by REL analysis identified only one site under moderate positive selection (BF ≥ 50) for UCP2 and UCP3 and our further analyses using more strict criteria (BF ≥ 100) did not support strong evidence for positive selection at these sites. Therefore, no valid conclusions could be drawn regarding the functional significance of these changes.
Analyses of vertebrate UCP evolution by Hughes and Criscuolo  and Saito et al.  suggest that UCP1-3 were acquired through two rounds of gene duplication. The first duplication produced UCP1 and the ancestral gene of UCP2/UCP3 whereas the second duplication produced UCP2 and UCP3. The results presented in this study confirm the previous conclusions that vertebrate UCP1-3 evolved from two successive duplications. The phylogenetic and syntenic analyses suggest that the first duplication (Figure 7) gave rise to UCP1 and UCP2/UCP3 ancestral gene took place prior to the divergence of vertebrates as evidenced by the presence of a homologue of UCP2 in early vertebrates (lampreys). The second round of duplication (Figure 7) that resulted in UCP2 and UCP3 occurred early in vertebrate evolution probably after the divergence of lampreys. Subsequent to these two duplications, UCP1 was lost from the avian and reptile lineages whereas UCP2 and UCP3 were lost from birds and amphibians, respectively (Figure 7). In addition to the two above mentioned duplications, a third round of duplication (Figure 7) occurred only in teleost fishes after they split from the tetrapod ancestors as evidenced by the absence of UCP3L in lampreys, amphibians, reptiles, birds and mammals. By taking a closer look at the chromosomal distribution of UCP genes in fish genomes, we found that UCP3L and UCP2/UCP3 are located on paralogous chromosomes in T. nigroviridis[44, 45] and O. latipes. These paralogous chromosomes arose from the whole genome duplication that occurred in ray-finned fish lineage around 350 million years ago [46–49]. Based on these observations, we speculate that UCP3L was generated in the ray-finned fish lineage as a result of a single event (fish-specific whole genome duplication) and not because of independent gene duplications.
The absence of UCP3L in zebrafish genome could thus be attributed either to the incompleteness of the genome assembly or to an independent loss of UCP3L in this species. To determine which of these phenomenon might be responsible for the UCP3L loss in zebrafish genome, we searched whether its flanking genes (CAMKK1 and C2CD3) are located on one or different contigs. We found that CAMKK1 and C2CD3 loci are located on contig CR450848.13, whose mapping to the sea bass genome assembly revealed higher synteny with chromosome 13 where UCP3L is located. Moreover, the re-annotation of the region harbouring CAMKK1 and C2CD3 loci did not reveal the presence of a UCP gene. Taken together, these observations suggest that UCP3L has been independently lost in zebrafish genome. Speculating about the reasons why UCP3L was lost only in zebrafish but not in the other teleost species is difficult without knowing the functional role of this gene in teleost fishes.
By combining phylogenetic and detailed syntenic analyses, we unequivocally identified four UCP gene family members in teleost genomes, of which three (UCP1, UCP2 and UCP3) are shared by major vertebrate lineages. Phylogenetic results revealed that the gene duplication events that gave rise to these three genes occurred in the common ancestor of vertebrates, probably prior the divergence of lampreys. The fourth UCP (UCP3L) that has been identified only in fish, derived from teleost-specific third-round whole genome duplication that occurred in a common ancestor of teleost fishes. Functional divergence analysis among UCP family members indicated that substantial altered functional constraints have occurred on all UCP paralogues after gene duplication, which may have led to the evolution of new functions. These results suggest that UCP genes might be crucial for the adaptation of teleost to diverse ecological niches. The critical amino acid residues for functional divergence identified here provide new insights into the functional evolution and diversification of UCP genes, and since knowledge on UCP function is limited especially in fishes, they offer a starting point for further experimental validations.
Identification of scaffolds containing UCP genes and gene structure analysis
The methods applied for sequence data production of sea bass are described in full detail in [50, 51]. To identify the scaffolds containing UCP genes, UCP1 protein sequence from stickleback, Gasteroteus aculeatus was blasted (TBLASTN, default parameters) against the sea bass draft genome assembly [Unpublished]. The resulting alignments were checked manually to identify the best hits considering score and identity values as well as a nearly complete alignment from start to end of the query. The matching scaffold fasta-files were converted to Game.xml databases and subsequently loaded into APOLLO Genome Curation Tool (V 1.9.6). Ab initio gene prediction was done with GENSCAN  to predict the genomic UCP gene structures. A homology-based prediction was conducted in parallel using UCP protein sequences from G. aculeatus using the SPALN software  together with APOLLO annotation curation tool. The stickleback proteins were used as informant sequences because its genome was identified to be the closest sequenced genome . Since the SPALN output file is not compatible to APOLLO input format, the stickleback protein sequences were first splice-aligned to the genomic scaffold sequences with the SPALN software. Predicted exon coordinates of the SPALN output were then converted to a sim4 compatible format, which then was processed by APOLLO. The combination of both approaches provides more information that help to improve the accuracy of the final gene models. The modelling of genes in D. labrax was then performed manually by combining the results of GENSCAN and SPALN predictions and setting the start and stop codons. The gene models were tested and annotated (corresponding name) by BLASTP (default parameters) against nrprot database. The flanking genes of each UCP were predicted in each species by ab initio and homology-based prediction as described above for UCP genes. When an UCP orthologue could not be found in a given species, the region bounded by the flanking genes was extracted and re-annotated by ab initio and homology-based prediction to determine whether there was miss-annotation.
Identification of sea bass UCP orthologues in other vertebrates
To identify orthologues in teleost fish species, the four UCP members identified in sea bass were blasted against zebrafish, medaka, takifugu, tetraodon and stickleback genomic sequences using the Ensembl genome browser server (Ensembl BLASTN, “distant homologies” settings). The upstream and downstream genes of each UCP member were identified in each species to determine whether they are conserved. The conservation of the flanking genes was then used to confirm that they are real orthologues of sea bass UCP members. Protein sequences of UCP gene family members of other vertebrates were also obtained from Ensembl genome browser or GenBank by BLASTP (Ensembl/NCBI default parameters) search. When a vertebrate orthologue could not be identified unambiguously, we searched for the flanking genes from fish to identify potential syntenic regions where UCP gene members would be located.
The predicted sea bass UCP amino acid sequences together with other teleost UCP genes as well as those identified in other vertebrates were aligned by MAFFT v6.864b [http://mafft.cbrc.jp/alignment/server] using default parameters. Amino acid sequence alignments were subsequently improved by removing the ambiguous positions using Gblocks [http://molevol.cmima.csic.es/castresana/Gblocks_server.html]. The JTT + G was selected as the best amino acid model on the final dataset comprised of total of 285 positions for teleost and 277 positions for all vertebrate including teleost using ProtTest v3.0 [http://darwin.uvigo.es/software/prottest3/prottest3.html]. The aligned amino acid data sets were used to construct the phylogenetic trees with maximum likelihood approach using PhyML v3.0 [http://www.atgc-montpellier.fr/phyml]. The teleost tree was rooted with invertebrate (Ciona intestinalis, Ciona savignyi and Caenorhabditis elegans) UCP sequences and the vertebrate tree with midpoint rooting as implemented in PhyML. The robustness of the tree topology was assessed by non parametric bootstrap analysis with 1,000 resampling replicates.
Analysis of selection pressures
The selection pressure was estimated by comparing nonsynonymous (dN) and synonymous (dS) substitution rates (ω = dN/dS) for each individual UCP gene. A dN/dS ratio of 1 is assumed as indicative of neutrality, dN/dS > 1 is indicative of positive selection and dN/dS < 1 is considered as a signature of purifying selection. Such analysis is mainly used to estimate the selective force acting on different alleles of a gene, but it can be also applied to duplicated genes with relatively low evolution rate, and which are not saturated in terms of synonymous substitutions. The dN/dS ratios of all pair-wise comparisons of UCP genes were calculated using the yn00 program in PAML . Additionally, we tested for selection among sites using Datamonkey online interface http://www.datamonkey.org which includes three methods [single likelihood ancestor counting (SLAC), fixed effects likelihood (FEL) and random effects likelihood (REL)] for detecting sites under selection. Among these methods, REL is the most powerful for detecting sites under selection particularly when dealing with small sample size of sequences or low sequence divergence. The REL method is an extension of codon-based selection analyses implemented in PAML. We have used REL method via the Datamonkey website instead of the models collected in the package PAML, because it allows both synonymous and nonsynonymous substitution rates to vary among sites. It has been demonstrated that the failure of modeling of dN and dS rate variation in a model can lead to misidentification of sites as positively selected  and the models collected in the package PAML do not allow modeling such variations. REL analysis calculates two Bayes factors (BF), one in the case of purifying or negative selection (dN < dS) and another for positive selection (dN > dS). A BF ≥ 50 is generally considered as an evidence for a moderate selection whereas a BF ≥ 100 indicates sites that have strong evidence positive selection. We considered sites to be under positive selection, if they met the initial criteria (BF ≥ 50) and further confirmed them with the more strict criteria (BF ≥ 100) for the detection of positive selection. The REL method was run on a neighbour joining phylogenetic tree after using the best substitution model (HKY85).
The coefficients of type-I and type-II functional divergence (θI and θII) between any two UCP clusters were used to estimate the level of functional divergence among UCP paralogues (UCP1, UCP2, UCP3 and UCP3L). θI and θII were calculated for each amino acid position in the teleost UCP protein sequence alignment (see Additional file 4) using the method of Gu [56, 57], as implemented in the DIVERGE v2.0 package. This method uses a maximum likelihood approach to assess significant changes in site-specific shift of evolutionary rate or site-specific shift of amino acid properties when comparing two clusters of duplicate genes. Type-I refers to functional divergence that occurred shortly after gene duplication as a result of site-specific changes in evolutionary rates between two clusters generated by gene duplication. In other words, it denotes amino acid residues that are conserved in one cluster but highly variable in the other, which implies that these residues have been subjected to different functional constraints. Type-II refers to amino acids that are highly conserved in both clusters but with very different chemical properties (i.e. positive versus negative charge). Large value of θI or θII (e.g. significantly greater than 0) supports the occurrence of functional divergence whereas θI or θII ≈ 0 indicates no functional divergence.
To determine which UCP cluster is functionally more divergent, we estimated the type-I functional distance between any two clusters, which is defined as dF = −ln(1 - θI). Wang and Gu  have shown that under the assumption of independence between two clusters A and B, dF is additive i.e. dF (AB) = dF(A) + bF(B), where bF(A) and bF(B) are the functional branch length of clusters A and B, respectively. Large bF value for a duplicate cluster is indicative of altered functional constraints at many amino acid positions whereas bF ≈ 0 indicates that there was no significant shift in function from an ancestral function after gene duplication. The UCP functional branch lengths were also estimated in other vertebrates using their protein sequence alignment (see Additional file 4).
Furthermore, amino acid residues that might be crucial for type-I or type-II functional divergence among UCP paralogues were predicted using the site (k)-specific score QI (k) or QII (k). The site (k)-specific score corresponds to the posterior probability that site k is related to type-I or type II functional divergence.
The authors are grateful to the picking, sequencing- and template preparation teams at MPI Molecular Genetics for tirelessly working on the sequencing of bacterial WGS clones. They are also grateful to Bruno Guinand for the valuable comments and to Christoph Kneip for drawing their attention to UCPs. This work was supported financially by the Max Planck Institute for Molecular Genetics, Germany. We also thank two anonymous reviewers for their constructive criticism of the previous version of this article.
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