Indels and imperfect duplication have driven the evolution of human complement receptor 1 (CR1) and CR1-like from their precursor CR1 alpha:: Importance of functional sets

被引:28
作者
McLure, CA
Williamson, JF
Stewart, BJ
Keating, PJ
Dawkins, RL
机构
[1] Univ Western Australia, Ctr Mol Immunol & Instrumentat, Canning Vale S, WA 6155, Australia
[2] CY OConnor ERADE Village, Canning Vale, WA, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
complement control protein; CR1; CR1-L; evolution; duplication; insertion and deletion;
D O I
10.1016/j.humimm.2005.01.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
This study examines the effects of duplication and insertions-deletions (indels) by comparing human complement receptor 1 (CR1) and human CRI-like (CR1L) with syntenic genes from four other vertebrates (chimpanzee, baboon, rat, and mouse). By phylogenetic analysis, the domains of these genes can be classified into 10 distinct subfamilies (a, b, c, d, e, f, g(-like), h, j, and k), which have been largely conserved throughout vertebrate and invertebrate evolution. In spite of many complex and diverse duplications and indels, the subfamily order of domains (a, j, e, f, b, k, d, g(-like)) has been maintained. The number of domain sets has increased progressively, thereby expanding the functional repertoire. (c) American Society for Histocompatibility and Immunogenetics, 2005. Published by Elsevier Inc.
引用
收藏
页码:258 / 273
页数:16
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