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人类 IRGM 基因“生或死”。

Human IRGM gene "to be or not to be".

机构信息

Department of Genome Sciences, University of Washington, Seattle, WA, USA.

出版信息

Semin Immunopathol. 2010 Dec;32(4):437-44. doi: 10.1007/s00281-010-0224-x. Epub 2010 Aug 25.

Abstract

The immunity-related GTPases (IRG proteins) are one of the strongest early resistance systems against intracellular pathogens. The IRG gene family contains 21 copies arranged as tandem gene clusters on two chromosomes in the C57BL/6 mouse genome but has been reduced to only two copies in humans: IRGC and IRGM. IRGC is not involved in immunity, but the human IRGM gene plays a role in autophagy-targeted destruction of Mycobacterium tuberculosis (BCG) and Salmonella typhimurium. Variant IRGM haplotypes have been associated with increased risk for Crohn's disease and correlated with differential expression of IRGM transcripts. This article reviews in detail the studies performed on human samples, in vitro, and in sequence analyses that provide evidence for the unusual evolutionary history of the IRGM locus and the important role of the IRGM gene in autophagy and Crohn's disease in response to pathogenesis.

摘要

免疫相关 GTPases(IRG 蛋白)是针对细胞内病原体的最强早期抗性系统之一。IRG 基因家族包含 21 个拷贝,在 C57BL/6 小鼠基因组的两条染色体上排列成串联基因簇,但在人类中已减少到仅 2 个拷贝:IRGC 和 IRGM。IRGC 不参与免疫,但人类 IRGM 基因在靶向自噬破坏结核分枝杆菌(BCG)和鼠伤寒沙门氏菌方面发挥作用。IRGM 单倍型变体与克罗恩病的风险增加有关,并与 IRGM 转录本的差异表达相关。本文详细回顾了在人类样本、体外和序列分析中进行的研究,这些研究为 IRGM 基因座的异常进化历史以及 IRGM 基因在自噬和克罗恩病对发病机制的反应中的重要作用提供了证据。

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