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东南亚三个种群中的新型食蟹猴MHC-DPB1多态性

Novel cynomolgus macaque MHC-DPB1 polymorphisms in three South-East Asian populations.

作者信息

Sano K, Shiina T, Kohara S, Yanagiya K, Hosomichi K, Shimizu S, Anzai T, Watanabe A, Ogasawara K, Torii R, Kulski J K, Inoko H

机构信息

Department of Molecular Life Science, Division of Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1143, Japan.

出版信息

Tissue Antigens. 2006 Apr;67(4):297-306. doi: 10.1111/j.1399-0039.2006.00577.x.

Abstract

Cynomolgus macaques (Macaca fascicularis, Mafa), alias the crab-eating monkeys or long-tailed macaques, live across a vast range of South-East Asia. These non-human primates have emerged as important animal models in infectious and chronic diseases and transplantation studies, necessitating a more extensive characterization of their major histocompatibility complex polymorphic regions. The current information on the polymorphic variation or diversity of the Mafa-DPB1 locus is largely limited in comparison with the more commonly studied rhesus macaque DPB1 locus. In this article, to better elucidate the degree and types of polymorphisms and genetic differences of Mafa-DPB1 locus among three South-East Asian populations and to investigate how the allele differences between macaques and humans might affect their respective immune responses, we identified 40 alleles within exon 2 of the Mafa-DPB1 locus by DNA sequencing using 217 individuals. We also performed evolutionary and population analyses using these sequences to reveal some population-specific alleles and trans-species allelic conservation between the cynomolgus macaques and the rhesus macaques. Of the 40 new alleles, eight belong to a newly identified lineage group not previously found in the rhesus macaque species. This allele information will be useful for medical researchers using the cynomolgus macaques in disease and immunological studies.

摘要

食蟹猕猴(Macaca fascicularis,Mafa),别名食蟹猴或长尾猕猴,广泛分布于东南亚地区。这些非人灵长类动物已成为传染病、慢性病及移植研究中的重要动物模型,因此需要对其主要组织相容性复合体多态性区域进行更广泛的特征描述。与研究更为普遍的恒河猴DPB1基因座相比,目前关于食蟹猕猴DPB1基因座多态性变异或多样性的信息非常有限。在本文中,为了更好地阐明东南亚三个种群中食蟹猕猴DPB1基因座的多态性程度、类型及遗传差异,并研究猕猴与人类之间的等位基因差异如何影响各自的免疫反应,我们通过对217只个体进行DNA测序,在食蟹猕猴DPB1基因座的第2外显子中鉴定出40个等位基因。我们还利用这些序列进行了进化和群体分析,以揭示一些种群特异性等位基因以及食蟹猕猴和恒河猴之间的跨物种等位基因保守性。在这40个新等位基因中,有8个属于一个新鉴定的谱系组,该谱系组在恒河猴物种中未曾发现。这些等位基因信息将有助于医学研究人员在疾病和免疫学研究中使用食蟹猕猴。

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