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恶性疟原虫var基因家族内的激活、沉默和相互排斥表达。

Activation, silencing and mutually exclusive expression within the var gene family of Plasmodium falciparum.

作者信息

Frank Matthias, Deitsch Kirk

机构信息

Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021, USA.

出版信息

Int J Parasitol. 2006 Aug;36(9):975-85. doi: 10.1016/j.ijpara.2006.05.007. Epub 2006 Jun 9.

Abstract

The var gene family of the human malaria parasite Plasmodium falciparum remains a topic of intense research focus due to the key role these antigen-encoding genes play in the ability of parasites to cause disease and avoid the human immune response. In recent years, as molecular tools for investigating the mechanisms that coordinate var gene expression have become more sophisticated, numerous insights have been acquired into how parasites manage to regulate transcription of this large gene family such that only a single gene is expressed at a time. The results of different experimental approaches have implicated mechanisms of chromatin modification, subnuclear localisation, promoter/promoter interactions and sterile RNAs in the silencing and activation of individual var genes, however, the roles that each of these different aspects play remain ill defined. In addition, some conflicting data regarding silencing and monoallelic expression of recombinant var promoters have recently been published, thus adding to the difficulty of understanding this complex phenomenon. In this review, we hope to present some of the existing data regarding this controversial topic in a way that will be both informative and constructive in our efforts to understand the molecular aspects of antigenic variation by malaria parasites.

摘要

由于这些编码抗原的基因在疟原虫致病及逃避人体免疫反应的能力中发挥关键作用,人类疟原虫恶性疟原虫的var基因家族仍是深入研究的焦点。近年来,随着用于研究协调var基因表达机制的分子工具变得更加精密,人们对疟原虫如何设法调控这个大基因家族的转录从而一次仅表达单个基因获得了诸多见解。不同实验方法的结果表明染色质修饰、亚核定位、启动子/启动子相互作用和无义RNA在单个var基因的沉默和激活中起作用,然而,这些不同方面各自所起的作用仍不清楚。此外,最近发表了一些关于重组var启动子沉默和单等位基因表达的相互矛盾的数据,从而增加了理解这一复杂现象的难度。在本综述中,我们希望以一种既信息丰富又具建设性的方式呈现关于这个有争议话题的一些现有数据,以助力我们理解疟原虫抗原变异的分子层面。

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