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一群中国恒河猴(猕猴)中主要组织相容性复合体II类DQB(MhcMamu - DQB1)等位基因的特征分析。

Characterization of the major histocompatibility complex class II DQB (MhcMamu-DQB1) alleles in a cohort of Chinese rhesus macaques (Macaca mulatta).

作者信息

Qiu Chen-Li, Yang Gui-Bo, Yu Kai, Li Yue, Li Xiao-Li, Liu Qiang, Zhao Hui, Xing Hui, Shao Yiming

机构信息

State Key Laboratory for Infectious Disease Prevention and Control, National Center for AIDS/STD Control and Prevention, Beijing 100050, People's Republic of China.

出版信息

Hum Immunol. 2008 Aug;69(8):513-21. doi: 10.1016/j.humimm.2008.05.014. Epub 2008 Jun 26.

Abstract

Rhesus macaques have long been used in animal models for various human diseases, the susceptibility and/or resistance to some of which have been associated with the major histocompatibilty complex (MHC). To gain insight into the MHC background and to facilitate the experimental use of Chinese rhesus macaques, the second exon of MhcMamu-DQB1 genes in 105 rhesus macaques were characterized by cloning and sequencing. A total of 37 MhcMamu-DQB1 alleles were identified, illustrating a marked allelic polymorphism at DQB1 in these monkeys. In addition to 10 alleles were novel sequences that had not been documented in earlier reports, at least 14 alleles reported in earlier studies were not detected in this study. Most of the sequences (73%) observed in this study belong to DQB1 06 (13 alleles) and DQB1 18 (14 alleles) lineages, and the rest (27%) belong to DQB1 15, DQB1 16 and DQB1 17 lineages. The most frequent allele detected among these monkeys was MhcMamu-DQB1 06111 (22%), followed by DQB1 1503 (19%); and most of the novel alleles were present at a frequency of less than 2.5%. As for individual animals, 24 of 105 (23%) were homozygous whereas 81 of 105 (77%) were heterozygous at the MhcMamu-DQB1 locus. These data indicated significant differences in MhcMamu-DQB1 allele distribution between the Chinese rhesus macaques and the previously reported rhesus macaques, which were mostly of Indian origin. This information will not only promote the understanding of rhesus macaque MHC diversity and polymorphism but will also facilitate the use of Chinese rhesus macaques in human disease studies, especially those that may be associated with HLA-DQB genes.

摘要

恒河猴长期以来一直被用于各种人类疾病的动物模型,其中一些疾病的易感性和/或抗性与主要组织相容性复合体(MHC)有关。为了深入了解MHC背景并促进中国恒河猴的实验应用,对105只恒河猴的MhcMamu - DQB1基因的第二个外显子进行了克隆和测序。共鉴定出37个MhcMamu - DQB1等位基因,表明这些猴子的DQB1存在明显的等位基因多态性。除了10个等位基因是早期报告中未记录的新序列外,本研究中未检测到早期研究报告的至少14个等位基因。本研究中观察到的大多数序列(73%)属于DQB1 06(13个等位基因)和DQB1 18(14个等位基因)谱系,其余(27%)属于DQB1 15、DQB1 16和DQB1 17谱系。在这些猴子中检测到的最常见等位基因是MhcMamu - DQB1 06111(22%),其次是DQB1 1503(19%);大多数新等位基因的频率低于2.5%。至于个体动物,105只中有24只(23%)在MhcMamu - DQB1位点是纯合子,而105只中有81只(77%)是杂合子。这些数据表明中国恒河猴与先前报道的主要为印度起源的恒河猴在MhcMamu - DQB1等位基因分布上存在显著差异。这些信息不仅将促进对恒河猴MHC多样性和多态性的理解,还将有助于中国恒河猴在人类疾病研究中的应用,特别是那些可能与HLA - DQB基因相关的研究。

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