BMC Evolutionary Biology BioMed Central

The integrins of the urochordate Ciona intestinalis provide novel insights into the molecular evolution of the vertebrate integrin family Abstract Background: Integrins are a functionally significant family of metazoan cell surface adhesion receptors. The receptors are dimers composed of an alpha and a beta chain. Vertebrate genomes encode an expanded set of integrin alpha and beta chains in comparison with protostomes such as drosophila or the nematode worm. The publication of the genome of a basal chordate, Ciona intestinalis, provides a unique opportunity to gain further insight into how and when the expanded integrin supergene family found in vertebrates evolved.


Background
The yellowfin tuna, Thunnus albacares, has a global distribution in tropical and sub-tropical oceans. Annual catches of yellowfin tuna have averaged 1.2 million metric tons since 1998 with sizes ranging from 5 to 20 kg [1]. If the average size of a harvested fish is 10 kg, then the harvest of 1.3 million metric tons in 2002 represents approximately 130 million individual fish.
In an earlier study, Scoles and Graves [2] were unable to find evidence of genetic differentiation between small samples of yellowfin tuna (Thunnus albacares) from the Atlantic (n = 20) and Pacific Oceans (n = 100) using an RFLP analysis of whole mitochondrial DNA (mtDNA). Subsequently, Ward et al. [3] found significant differentiation at the GPI-A* allozyme locus but only weak evidence for genetic differentiation with an RFLP analysis of whole mtDNA. In the whole mtDNA study, much larger sample sizes were employed to increase the sensitivity of the mtDNA assay, but only two restriction enzymes were used and consequently, only a few restriction sites were analyzed. The GPI-A* data were consistent with earlier studies that demonstrated genetic differentiation between Eastern and Western Pacific samples [4,5].
Skipjack tuna (Katsuwonus pelamis) are found in tropical and warm temperate waters of the world's oceans. They are present in the three major oceans in large numbers and comprise approximately 40% of the annual catch of the world's tunas. Annual catches are on the order of 2 million metric tons or approximately 670 million individuals per year [1]. Despite their huge numbers, the skipjack tuna are not as well studied as most members of the genus Thunnus. Tagging studies have demonstrated limited seasonal movements, but not much transoceanic movement. Thus, they probably do not spawn at discrete locations [6].
In the Pacific, genetic studies using isozymes have demonstrated an East-West cline in a serum esterase allele [7][8][9]. Fujino et al. [10] also demonstrated differences in esterase allele frequencies in samples from the Atlantic, Indian, and Pacific Oceans. However, small samples of Atlantic (n = 7) and Pacific (n = 9) skipjack appeared identical when mtDNA was examined [11].
After the formation of the Isthmus of Panama, the potential contact between Atlantic and Indo-Pacific populations was limited to the waters around southern Africa. It appears that this separation of the Atlantic and Pacific Oceans resulted in significant genetic drift for many large pelagic fishes since these subpopulations are now genetically differentiated. Examples include bigeye tuna [12,13], albacore [14,15], swordfish [16,17], blue marlin [18] and sailfish [19]. In addition, even more pronounced differentiation produced species pairs of Atlantic and Pacific bluefin tunas and the Atlantic white marlin and the Pacific striped marlin [19][20][21][22].
To measure the degree of genetic differentiation between the Atlantic and Pacific sub-populations of either yellowfin or skipjack tuna, we examined the hypervariable control region I (CR-I) and a segment of a coding region gene of the respective mitochondrial DNAs. Genetic differences were observed between the Atlantic and Pacific yellowfin tuna samples with PCR-RFLP data of the ATCO gene region, but not with CR-I sequence data. In contrast, no differences between the Atlantic and Pacific skipjack tuna samples were detected with either type of data. Information contained in the CR-I reveals very different demographic histories for yellowfin tuna and skipjack tuna. However, very large long-term female effective population sizes (N e ) were estimated for both species, which may explain the observed levels of inter-oceanic genetic partitioning.

Control region nucleotide sequence analysis
A total of 333 bp of the nucleotide sequence of the mitochondrial DNA (mtDNA) control region was determined for 148 yellowfin tuna (Table 1 and GenBank accession numbers AY899520 -AY899681). For the pooled sample of yellowfin tuna, 110 variable sites defined 130 haplotypes (h = 0.997) and a nucleotide diversity (π) of 3.5%. Diversity indices for each locality sampled were also high, although values of π and h were slightly lower for the NW Atlantic yellowfin sample where five haplotypes were repeated twice. For skipjack tuna, a total of 394 bp was determined for 115 individuals ( Table 2 and GenBank accession numbers AY899405 -AY899519). In the pooled skipjack tuna sample, there were 157 variable sites defining 111 haplotypes, resulting in a very high value of haplotypic diversity (h = 0.999). Nucleotide diversity (π = 8.4%) was more than twice as high in skipjack tuna as in yellowfin tuna. All of the sampling localities of skipjack tuna had very high diversity values (π >7.7%; h > 0.998). For both species, the high haplotypic diversity values are consistent with the observed large census population sizes (N c ). Phylogenetic analyses resulted in very different trees for each species. The CR-I gene-tree topology of skipjack tuna is much larger and better structured than the yellowfin tuna phylogeny, and contains multiple branches with high bootstrap proportion support ( Figure 1). However, there is no obvious phylogeographic association in either species, with CR-I lineages from different basins scattered throughout the phylogenetic trees. As a consequence, in both yellowfin tuna (Table 3) and skipjack tuna (Table 4), the majority of the genetic variation corresponds to differences between individuals within populations, and only a minor fraction of the variation corresponds to differences among-groups. Thus, in both species, the control region sequences provide no evidence of genetic differentiation between Atlantic and Indo-Pacific sub-populations.

RFLP analysis of the mitochondrial ATCO gene region
We hypothesized that the high mutation rate of the control region might have resulted in homoplasy and high levels of haplotypic diversity that masked the actual genetic divergence of Atlantic and Pacific mtDNAs in these species. Analysis of a gene that has a lower mutation rate than that of the control region has been used to reveal genetic divergence in bigeye tuna [13]. Therefore, we performed a nucleotide sequence analysis on the yellowfin tuna mitochondrial ATCO gene region since variation had been shown previously for this gene [23,24]. We found mutations at two positions that resulted in the loss of restriction sites for the enzymes DdeI and HpyCH4III, respectively. When amplified Atlantic and Indo-Pacific yellowfin ATCO DNAs were analyzed with these two enzymes, most DNAs were cut with both enzymes (Table  5). However, DNAs that had lost either one of the two restriction sites were more common in the Atlantic sample than in the Indo-Pacific sample. When the haplotype dis-      tributions were compared, the differences were found to be significant with 7% of the variation occurring between samples (Table 6). Thus, low levels of genetic differentiation have occurred between the two yellowfin sub-populations. When the haplotypes were mapped to a neighbour-joining tree of the control region sequences, the mutations affecting the restriction sites were clustered, suggesting that each mutation had occurred once prior to separation of the two sub-populations (data not shown). This result is consistent with a slower rate of mutation in the ATCO gene region compared to that of the control region.
Similar experiments were performed with the skipjack tuna samples. Two variable sites had been observed in the mitochondrial cytochrome b (cytB) gene by Terol et al. [25]. Since one of these sites could not be assayed with restriction enzymes, we determined the nucleotide sequence of this portion of the cytB gene for each DNA in the Atlantic and Pacific skipjack tuna samples. Little additional variation was observed, and allele frequencies were similar in the two samples (Table 7). When the haplotype distributions were compared, all of the variation occurred within samples. Thus, there is no evidence for genetic differentiation between the Atlantic and Pacific sub-populations of skipjack tuna.

Demographic history and effective population size
The unimodal mismatch distribution for the pooled sample of yellowfin tuna ( Figure 2) and a significant Tajima D test (Table 1) both suggest the historical expansion of this population. In sharp contrast, the skipjack mismatch distribution is bimodal ( Figure 2) and the neutrality test is not significant ( Table 2), suggesting that the effective size of the skipjack population has been large and stable for a long period. In fact, the value of θ 0 suggests that the number of females in the skipjack population was originally large (N e0 = 320,000) whereas the effective number of yellowfin tuna females prior to expansion was small (N e0 = 823). However, the values of θ 1 suggest large long-term numbers of effective female breeders (N e1 ) of about 98 million for skipjack tuna and about 10 million for yellowfin tuna.

Discussion
Compared to other scombroid species with cosmopolitan distributions, we found substantially less genetic differentiation between Atlantic and Pacific sub-populations of yellowfin tuna and no inter-oceanic genetic differentiation of skipjack tuna. For instance, in bigeye tuna, there are two highly divergent mtDNA clades, one is cosmopolitan and the other is endemic to the Atlantic [12,13]. This asymmetric distribution of Atlantic and Pacific clades has been observed in other large pelagic fishes as well, including swordfish [16,17], blue marlin [18], and sailfish [19,26]. Similarly, the striped marlin (Pacific) and white marlin (Atlantic) and the Atlantic bluefin tuna and the Pacific bluefin tuna are considered to be pairs of sister species [19][20][21]26]. Thus, significant differentiation has occurred between the Atlantic and Pacific populations of many large pelagic species. Why are skipjack and yellowfin tuna populations different? One possibility is that in contrast to other large pelagic species, sufficient gene flow occurs to prevent inter-oceanic genetic differentiation. However, this explanation is contrary to the distribution patterns of tunas and billfish [27,28]. For instance, bigeye tuna has a distribution of catches that would suggest a population continuum from the Indian Ocean to South Atlantic waters along the east and west coasts of Africa. However, bigeye samples show   Mismatch distributions for the entire sample of a) yellowfin tuna and b) skipjack tuna Yellowfin tuna Skipjack tuna a marked inter-oceanic differentiation [12,13]. In the Indian Ocean, the presence of skipjack and yellowfin tuna south of 20° S, is confined to the warm waters associated with the Agulhas currents. Seasonal movements do occur around the Cape of Good Hope via the Agulhas current, but it appears that the migrant tuna and other pelagic species return to the Indian Ocean as the seasons change [13,29]. In fact, the distribution patterns of these two species in the South Atlantic along the African coast of are remarkably similar to both blue marlin and sailfish, two species that show a pronounced differentiation between Indo-Pacific and Atlantic populations. It should be noted, however, that the presence of "Pacific" mitochondrial DNA clades in Atlantic subpopulations of many tuna species indicates that inter-oceanic migration has occurred in the past. However, contemporary levels of inter-oceanic genetic differentiation for these species indicate that current levels of gene flow are absent or severely reduced. Thus, current distribution patterns of skipjack tuna and yellowfin tuna are not consistent with substantial levels of inter-oceanic gene flow. Certainly, there is no evidence to suggest that gene flow is occurring or has occurred at levels higher in these two species than in any of the other pelagic species where interoceanic differentiation has been demonstrated.
An alternative explanation to account for the lack of interoceanic differentiation in skipjack tuna and yellowfin tuna, is that the time since population expansion began has not been sufficient to allow for the populations to become differentiated. Assuming the very conservative mutation rate for CR-I of 4.9% per million years, a generation time 3.5 years, and the tau value 8.52, expansion of yellowfin tuna occurred about 522 Ky ago. By comparison, the estimated time for genetic differentiation of the Atlantic and Pacific populations of swordfish and of the Atlantic and Pacific bluefin tunas, using the same mutation rate, is very similar (450-470 Ky), and an even shorter time (170 Ky) is sufficient to explain the substan-tial genetic differentiation between the Atlantic and Mediterranean swordfish populations [30]. Thus, time since expansion cannot explain the absence of inter-oceanic differentiation in these species. Therefore, we propose that much larger effective population sizes are the primary factor responsible for the similarity of the Atlantic and Pacific sub-populations of skipjack and yellowfin tuna.
Among large pelagic species, the female effective population size can be estimated from the demographic estimates obtained from the CR-I sequences of Atlantic bluefin tuna and swordfish. Assuming a mutation rate of 4.9% per million years and a generation time of 6 years, the female N e estimates are 900,000 for bluefin tuna and 800,000 for swordfish [30]. Effective population sizes have not been estimated for other species of tunas, but annual harvest data are generally used as a proxy for abundance since the commercial harvest of large fish has become quite efficient throughout the world's oceans and harvest restrictions have only incremental impact on the total harvest of any species. Furthermore, haplotypic diversities of tuna mitochondrial DNAs are approximately 99% in all tuna species [12,31], suggesting that female reproductive variance is small. Accordingly, census population size can be expected to be proportional to effective population size in tuna species. The estimated number of skipjack and yellowfin caught in the year 2002 is 670 million and 130 million, respectively ( Table 8). The catch of all other tunas was 24 million individuals or less. Thus, the abundance of skipjack tuna is approximately 5 times that of yellowfin, and more than 300 times that of Atlantic bluefin tuna and swordfish. These estimates of abundance from fisheries data appear to correspond well with the estimated female N ef values. The observed correspondence does not take into consideration dramatic changes in abundance of some of these species over the last 20 years, nor sex ratio differences, or the age distribution of the catch (e.g., number of mature females). However, the comparison supports the hypothesis that skipjack tuna and yellowfin tuna, which are the two most abundant species, also have the largest effective population sizes, and the lowest amounts of genetic partitioning compared to other scombroid fishes.
Bigeye tuna, and bluefin tuna have much greater levels of genetic differentiation between Atlantic and Pacific subpopulations when mitochondrial DNA control region sequences are compared [12,31]. However, their population sizes are 6 and 15 times lower than that of yellowfin and 30 and 75 times lower than that of skipjack, respectively. Furthermore, since bluefin tuna are a more temperate species, their effective population sizes may have been significantly lower than those observed in recent times whenever the northern hemisphere experienced glacial maxima. Thus, the relative differentiation of the Atlantic and Pacific subpopulations is consistent with the demographics of these species of tuna.
One exception to the patterns described above is albacore tuna. The distribution of albacore tuna mitochondrial DNAs does not appear to fit the patterns described above for the other temperate tuna species. Albacore abundance is similar to that of bigeye tuna and both species have two mtDNA clades. However, in albacore the two clades are not as well differentiated nor do they display the phylogeographic association observed for the bigeye tuna clades [12]. Instead, the bimodal mismatch distribution of pairwise differences in albacore mtDNA is concordant with very large long-term effective population sizes in contrast to the contemporary population size.

Conclusion
Much lower levels of genetic differentiation were found among sub-populations of yellowfin tuna compared to those observed for other large tunas, probably due to the large population size of yellowfin tuna. Since skipjack tuna appear to have even larger population sizes than yellowfin tuna, it is not surprising that no genetic differentiation was observed between Atlantic and Pacific samples of these fish.

Methods
Samples of yellowfin tuna were obtained from the eastern Pacific Ocean (near the equator at 110° W; n = 41), the Indian Ocean (n = 63), the Gulf of Mexico and the East Coast of Florida (n = 38) and the Gulf of Guinea (n = 100). Samples of skipjack tuna were obtained from the Northwest Atlantic (n = 31), off the coast of Brazil (n = 19), the eastern Pacific Ocean (n = 43), and the south Pacific near the Solomon Islands (n = 37). DNA isolation, mitochondrial DNA D-loop region amplification, and nucleotide sequence analyses have been described previously [12,32]. The number of segregating sites (S) was estimated with MEGA. Values of haplotypic diversity (h) [33], nucleotide diversity (π) [34] and the mean number of pairwise differences (K) were computed in ARLEQUIN ver. 2.0 [35]. Mitochondrial DNA haplotype phylogenies were estimated using neighbour-joining analyses [36] with Tamura-Nei distances (α = 0.5)) in MEGA [37]. The pair-deletion option was used when missing data, insertions, or deletions were present. Maximum-Parsimony (MP) [38,39] was carried using heuristic searches with the default options in PAUP* 4.0b10 [40]. Statistical support for the nodes was estimated with 1000 non-parametric bootstrap replicates [41]. All trees were rooted at midpoint. Analyses of molecular variance (AMOVA) [42] were performed to estimate the partitioning of genetic variation in regional hierarchical arrangements using ARLEQUIN.
The demographic history contained in the mtDNA CR-I sequence data was inferred using two approaches. First, the null hypothesis of neutrality may be rejected when a population has experienced population expansion [43]. Accordingly, Tajima's D test of neutrality [43,44] and its significance levels were estimated using DnaSP 4.00 [45] based on 1000 simulated re-samplings replicates. Alternatively, a population that has experienced a rapid expansion in the recent past shows smooth wave-like mismatch distribution [46,47]. Thus, mismatch distribution analyses, under the assumption of selective neutrality, were also used to evaluate possible historical events of population growth and decline [47,48]. Past demographic parameters, including τ [49], θ 0 and θ 1 and their probabilities [47] were estimated in ARLEQUIN taking into account the heterogeneity of mutation rates [35].
For the analysis of the mitochondrial cytochrome b gene, a 650 bp fragment of the skipjack tuna cytochrome b gene was amplified using primers CB3 (GGCAAATAGGAAR-TATCATTC) and GLUDG (TGACTTGAARAACCAY-CGTTG) [50]. Alleles were identified by determining the nucleotide sequence of the amplified fragment. For yellowfin tuna, the ATCO gene region was amplified using primers H9342 (GCCATATCGTAGCCCTTTTTG) and L8562 (CTTCGACCAATTTATGAGCCC) [24]. The amplified fragments were digested with either DdeI or HpyCH4III and the digestion products were resolved by electrophoresis in a 1.2% agarose gel.