Lu C C, Ye Y, She J X, Bonhomme F, Wakeland E K
Department of Pathology, College of Medicine, JHMHC, University of Florida, Gainesville 32610-0275, USA.
Immunogenetics. 1996;43(3):115-24. doi: 10.1007/BF00176672.
Major histocompatibility complex (Mhc) class II Ab genes have evolved into three distinct lineages. While lineage 2 alleles differ from lineage 1 alleles by the insertion of a retroposon in intron 2, the basis for the extremely large intron 2 in lineage 3 alleles has heretofore been undetermined. In this report, we demonstrate by nucleotide sequencing that the genomic sequences of prototypic alleles from all three lineages diverge significantly and that lineage 3 is derived from lineage 2 by two insertional events in intron 2. One insert, composed of a member of B1 short interspersed repetitive elements (SINEs), occurs 508 base pairs (bp) 3' of exon 2, and the other, 1141 bp 3' of exon 2 within the retroposon that distinguishes lineage 2 from lineage 1. To assess the evolutionary stability of these lineages and the extent of ancestral polymorphisms of Ab within Mus species, we extended our restriction site polymorphism analysis to include 86 alleles from 120 independently derived H2 haplotypes from 12 separate species and subspecies of Mus. A phylogenetic tree revealing the relationships of these Ab alleles with respect to restriction site polymorphisms, but excluding the retroposon insertions, demonstrated that these lineages have distinctive genomic structures beyond the retroposon polymorphisms. In summary, these mouse Ab genes were produced from successive retroposon insertion events. Lineage 1 and 2 were detected in a variety of Mus species, including Mus caroli, indicating that these lineages diverged more than 2 million years ago. Lineage 3 alleles were found only in the Mus musculus subspecies, suggesting that it diverged from lineage 2 more recently. These results indicate that all three lineages of Ab have persisted through several speciation events in the genus Mus.
主要组织相容性复合体(Mhc)II类抗体基因已进化为三个不同的谱系。虽然谱系2等位基因与谱系1等位基因的区别在于内含子2中插入了一个反转录转座子,但谱系3等位基因中极大的内含子2的形成基础迄今尚未确定。在本报告中,我们通过核苷酸测序证明,所有三个谱系的原型等位基因的基因组序列存在显著差异,并且谱系3是通过内含子2中的两次插入事件从谱系2衍生而来的。一次插入由B1短散在重复元件(SINEs)的一个成员组成,发生在外显子2下游508个碱基对(bp)处,另一次插入在外显子2下游1141 bp处,位于区分谱系2和谱系1的反转录转座子内。为了评估这些谱系的进化稳定性以及小家鼠属内抗体祖先多态性的程度,我们扩展了限制性酶切位点多态性分析,纳入了来自小家鼠属12个不同物种和亚种的120个独立衍生的H2单倍型中的86个等位基因。一棵揭示这些抗体等位基因在限制性酶切位点多态性方面关系(但不包括反转录转座子插入)的系统发育树表明,这些谱系除了反转录转座子多态性外,还具有独特的基因组结构。总之,这些小鼠抗体基因是由连续的反转录转座子插入事件产生的。在包括稻鼠在内的多种小家鼠属物种中检测到了谱系1和2,这表明这些谱系在200多万年前就已经分化。仅在小家鼠亚种中发现了谱系3等位基因,这表明它是最近才从谱系2分化出来的。这些结果表明,抗体的所有三个谱系在小家鼠属的几次物种形成事件中都得以保留。