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布氏锥虫抗原变异的分子调控

The molecular control of antigenic variation in Trypanosoma brucei.

作者信息

Horn David

机构信息

Infectious & Tropical Diseases, London School of Hygiene & Tropical Medicine, Keppel Street, London WC1E 7HT, UK.

出版信息

Curr Mol Med. 2004 Sep;4(6):563-76. doi: 10.2174/1566524043360078.

Abstract

The African trypanosome, Trypanosoma brucei, is a protozoan that causes sleeping sickness in humans and N'gana in livestock. These flagellated parasites are directly exposed to immune defences as they circulate in the mammalian host bloodstream but they maintain persistent infections by undergoing antigenic variation. Central to this process is mono-allelic transcription and switching of the expressed variant-surface glycoprotein (VSG) gene which encodes the vast majority of their dense surface coat. The active telomeric VSG is transcribed by RNA polymerase I in an 'expression site body' (ESB) while transcription attenuation occurs at 'inactive' telomeres. Here, I review what is known about the molecular mechanisms involved in achieving antigenic variation and outline how we intend to exploit genome sequence and new tools, particularly RNA interference, to identify and characterise factors required for VSG regulation.

摘要

非洲锥虫,即布氏锥虫,是一种原生动物,可导致人类患昏睡病以及家畜患那加那病。这些具鞭毛的寄生虫在哺乳动物宿主血液中循环时直接暴露于免疫防御之下,但它们通过抗原变异维持持续性感染。这一过程的核心是单等位基因转录以及表达的可变表面糖蛋白(VSG)基因的转换,该基因编码其绝大多数致密表面被膜。活跃的端粒VSG由RNA聚合酶I在“表达位点体”(ESB)中进行转录,而转录衰减则发生在“非活跃”端粒处。在此,我综述了关于实现抗原变异所涉及的分子机制的已知信息,并概述了我们打算如何利用基因组序列和新工具,特别是RNA干扰,来鉴定和表征VSG调控所需的因子。

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