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灵长类主要组织相容性复合体的Alu元件

Alu elements of the primate major histocompatibility complex.

作者信息

Mnuková-Fajdelová M, Satta Y, O'hUigin C, Mayer W E, Figueroa F, Klein J

机构信息

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

出版信息

Mamm Genome. 1994 Jul;5(7):405-15. doi: 10.1007/BF00357000.

DOI:10.1007/BF00357000
PMID:7919653
Abstract

The chromosomal region constituting the major histocompatibility complex (MHC) has undergone complex evolution that is often difficult to decipher. An important aid in the elucidation of the MHC evolution is the presence of Alu elements (repeats) which serve as markers for tracing chromosomal rearrangements. As the first step toward the establishment of sets of evolutionary markers for the MHC, Alu elements present in selected MHC haplotypes of the human species, the gorilla, and the chimpanzee were identified. Restriction fragments of cosmid clones from the libraries of the three species were hybridized with Alu-specific probes, Alu elements were amplified by the polymerase chain reaction, and the amplification products were sequenced. In some cases, sequences of the regions flanking the Alu elements were also obtained. Altogether, 31 new Alu elements were identified, representing six Alu subfamilies. The average density of Alu elements in the MHC is one element per four kilobases (kb) of sequence. Alu elements have apparently been inserted steadily into the MHC over the last 65 million years (my). On average, one Alu element is inserted into the primate MHC every 4 my. Analysis of the human DR3 haplotype supports its origin by duplication from an ancestral haplotype consisting of DRB1 and DRB2 genes. The sharing of an old Alu element by the DRB1 and DRB2 genes, in turn, supports their divergence from a common ancestor more than 55 my ago.

摘要

构成主要组织相容性复合体(MHC)的染色体区域经历了复杂的进化过程,往往难以解读。阐明MHC进化的一个重要辅助手段是存在Alu元件(重复序列),它们可作为追踪染色体重排的标记。作为建立MHC进化标记集的第一步,已鉴定出人类、大猩猩和黑猩猩选定MHC单倍型中存在的Alu元件。来自这三个物种文库的黏粒克隆的限制性片段与Alu特异性探针杂交,通过聚合酶链反应扩增Alu元件,并对扩增产物进行测序。在某些情况下,还获得了Alu元件侧翼区域的序列。总共鉴定出31个新的Alu元件,代表六个Alu亚家族。MHC中Alu元件的平均密度为每4千碱基(kb)序列中有一个元件。在过去6500万年(my)中,Alu元件显然一直在稳定地插入到MHC中。平均而言,每400万年就有一个Alu元件插入到灵长类动物的MHC中。对人类DR3单倍型的分析支持其起源于由DRB1和DRB2基因组成的祖先单倍型的复制。DRB1和DRB2基因共享一个古老的Alu元件,反过来又支持它们在5500多万年前从一个共同祖先分化而来。

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2
Primate DRB genes from the DR3 and DR8 haplotypes contain ERV9 LTR elements at identical positions.来自DR3和DR8单倍型的灵长类DRB基因在相同位置含有ERV9长末端重复序列元件。
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引用本文的文献

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2
Similar patterns of genetic diversity and linkage disequilibrium in Western chimpanzees (Pan troglodytes verus) and humans indicate highly conserved mechanisms of MHC molecular evolution.西部低地大猩猩(Pan troglodytes verus)和人类的遗传多样性和连锁不平衡具有相似模式,表明 MHC 分子进化的高度保守机制。
BMC Evol Biol. 2020 Sep 15;20(1):119. doi: 10.1186/s12862-020-01669-6.
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本文引用的文献

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Primate DRB genes from the DR3 and DR8 haplotypes contain ERV9 LTR elements at identical positions.来自DR3和DR8单倍型的灵长类DRB基因在相同位置含有ERV9长末端重复序列元件。
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Different modes of Mhc evolution in primates.灵长类动物中主要组织相容性复合体(Mhc)的不同进化模式。
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6
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Mamm Genome. 1993;4(3):159-70. doi: 10.1007/BF00352232.
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Map of the human MHC.人类主要组织相容性复合体图谱。
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