Mhc class IIB gene evolution in East African cichlid fishes

被引:47
作者
Figueroa, F
Mayer, WE
Sültmann, H
O'hUigin, C
Tichy, H
Satta, Y
Takezaki, N
Takahata, N
Klein, J
机构
[1] Max Planck Inst Biol, Immunogenet Abt, D-72076 Tubingen, Germany
[2] Grad Univ Adv Studies, Dept Biosyst Sci, Kanagawa 2400193, Japan
关键词
major histocompatibility complex; haplochromines; convergent evolution; gene conversion; Oreochromis;
D O I
10.1007/s002510000181
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A distinctive feature of essential major histocompatibility complex (Mhc) loci is their polymorphism characterized by large genetic distances between alleles and long persistence times of allelic lineages. Since the lineages often span several successive speciations, we investigated the behavior of the Mhc alleles during or close to the speciation phase. We sequenced exon 2 of the class II B locus 4 from 232 East African cichlid fishes representing 32 related species. The divergence times of the (sub)species ranged from 6000 to 8.4 million years. Two types of evolutionary analysis were used to elucidate the pattern of exon 2 sequence divergence. First, phylogenetic methods were applied to reconstruct the most likely evolutionary pathways leading from the last common ancestor of the set to the extant sequences, and to assess the probable mechanisms involved in allelic diversification. Second, pairwise comparisons of sequences were carried out to detect differences seemingly incompatible with origin by nonparallel point mutations. The analysis revealed point mutations to be the most important mechanism behind allelic divergences, with recombination playing only an auxiliary part. Comparison of sequences from related species revealed evidence of random allelic (lineage) losses apparently associated with speciation. Sharing of identical alleles could be demonstrated between species that diverged 2 million years ago. The phylogeny of the exon was incongruent with that of the flanking introns, indicating either a high degree of convergent evolution at the peptide-binding region-encoding sites, or intron homogenization.
引用
收藏
页码:556 / 575
页数:20
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