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主要组织相容性复合体的分子谱系

The molecular descent of the major histocompatibility complex.

作者信息

Klein J, Satta Y, O'hUigin C, Takahata N

机构信息

Max-Planck-Institut für Biologie, Abteilung Immungenetik, Tübingen, Germany.

出版信息

Annu Rev Immunol. 1993;11:269-95. doi: 10.1146/annurev.iy.11.040193.001413.

Abstract

In the last few years, more than 500 primate major histocompatibility complex (Mhc) genes or parts thereof have been sequenced. The extraordinary sequence information is used here to draw conclusions about the manner of Mhc evolution. The Mhc genes are found to evolve at a relatively slow rate with the regularity of a clock. It takes from 1 to 6 million years for a new mutation to be incorporated into an Mhc allele, and the mutation rate is comparable to that of most other primate genes. The nonsynonymous sites coding for the peptide-binding region (PBR) are under relatively weak positive selection pressure (selection coefficient of a few percent only); the nonsynonymous non-PBR sites are under moderate negative selection pressure. The positive pressure is probably provided by parasites and is responsible for the trans-species persistence of allelic lineages at functional Mhc loci for more than 40 million years.

摘要

在过去几年里,超过500个灵长类动物主要组织相容性复合体(Mhc)基因或其部分已被测序。此处利用这些非凡的序列信息来推断Mhc的进化方式。发现Mhc基因以相对较慢的速度像时钟一样有规律地进化。一个新突变纳入Mhc等位基因需要100万到600万年,其突变率与大多数其他灵长类基因相当。编码肽结合区域(PBR)的非同义位点受到相对较弱的正选择压力(选择系数仅为百分之几);非同义非PBR位点受到中等程度的负选择压力。正选择压力可能由寄生虫提供,并导致功能性Mhc位点的等位基因谱系跨物种持续存在超过4000万年。

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