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30 个围绕 KIR2DL5 的等位基因水平单倍型定义了非裔美国人种群的多样性。

Thirty allele-level haplotypes centered around KIR2DL5 define the diversity in an African American population.

机构信息

Department of Pediatrics, Georgetown University Medical Center, Washington, DC 20057, USA.

出版信息

Immunogenetics. 2010 Aug;62(8):491-8. doi: 10.1007/s00251-010-0458-8. Epub 2010 Jun 29.

Abstract

KIR2DL5 alleles were physically linked to alleles at adjacent KIR loci to define this region of KIR haplotypes in 55 gene-positive random African Americans. The majority carried KIR2DL5B. Three KIR2DL5A and six KIR2DL5B alleles that have been previously described and 11 novel KIR2DL5 alleles were identified by DNA sequencing. Novel alleles included variation that may impact promoter activity; two alleles carried nonsynonymous coding region variation. Based on linkage with KIR2DS1, KIR2DS3, KIR2DS5, KIR2DL2, KIR2DL3, and KIR3DS1 alleles, seven haplotypes of KIR2DL5A and 23 haplotypes of KIR2DL5B were observed. The phylogenetic relationships among the KIR2DL5 alleles predicted their association with either KIR2DS3 (six alleles) or KIR2DS5 (seven alleles). All of the KIR2DL5A alleles were linked either to KIR3DS101301 or KIR3DS1049N. The majority of the KIR2DL5B alleles were linked to seven KIR2DL2 alleles; two were linked to a novel allele of KIR2DL3. These findings underscore the diversity of KIR haplotypes present in this population.

摘要

KIR2DL5 等位基因与相邻 KIR 基因座的等位基因物理相连,从而定义了 55 个随机非洲裔美国人中 KIR 单倍型的这一区域。大多数人携带 KIR2DL5B。通过 DNA 测序,鉴定了之前描述过的 3 个 KIR2DL5A 和 6 个 KIR2DL5B 等位基因,以及 11 个新的 KIR2DL5 等位基因。新的等位基因包括可能影响启动子活性的变异;两个等位基因携带非同义编码区变异。根据与 KIR2DS1、KIR2DS3、KIR2DS5、KIR2DL2、KIR2DL3 和 KIR3DS1 等位基因的连锁,观察到 KIR2DL5A 的 7 种单倍型和 KIR2DL5B 的 23 种单倍型。KIR2DL5 等位基因之间的系统发育关系预测了它们与 KIR2DS3(6 个等位基因)或 KIR2DS5(7 个等位基因)的关联。所有的 KIR2DL5A 等位基因要么与 KIR3DS101301 要么与 KIR3DS1049N 连锁。大多数 KIR2DL5B 等位基因与 7 个 KIR2DL2 等位基因连锁;两个与 KIR2DL3 的一个新等位基因连锁。这些发现强调了该人群中存在的 KIR 单倍型的多样性。

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