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成簇规律间隔短回文重复序列(CRISPR)基因多样性研究作为一种手段来重建结核分枝杆菌复合群的进化。

Clustured regularly interspersed short palindromic repeats (CRISPR) genetic diversity studies as a mean to reconstruct the evolution of the Mycobacterium tuberculosis complex.

作者信息

Sola Christophe

机构信息

Institut de Biologie Intégrative de la Cellule (I2BC), CEA, CNRS, Université Paris-Saclay, Orsay, France.

出版信息

Tuberculosis (Edinb). 2015 Jun;95 Suppl 1:S159-66. doi: 10.1016/j.tube.2015.02.029. Epub 2015 Feb 14.

Abstract

The natural history of tuberculosis may be tackled by various means, among which the record of molecular scars that have been registered by the Mycobacterium tuberculosis complex (MTBC) genomes transmitted from patient to patient for tens of thousands years and possibly more. Recently discovered polymorphic loci, the CRISPR sequences, are indirect witnesses of the historical phage-bacteria struggle, and may be related to the time when the ancestor of today's tubercle bacilli were environmental bacteria, i.e. before becoming intracellular parasites. In this article, we present what are CRISPRs and try to summarize almost 20 years of research results obtained using the genetic diversity of the CRISPR loci in MTBC as a perspective for studying new models. We show that the study of the diversity of CRISPR sequences, thanks to «spoligotyping», has played a great role in our global understanding of the population structure of MTBC.

摘要

结核病的自然史可以通过多种方式来研究,其中包括记录结核分枝杆菌复合群(MTBC)基因组中留存的分子印记,这些印记在患者之间传播了数万年甚至更久。最近发现的多态性位点——CRISPR序列,是历史上噬菌体与细菌斗争的间接证据,可能与当今结核杆菌的祖先作为环境细菌的时期有关,即它们成为细胞内寄生虫之前的时期。在本文中,我们介绍了CRISPRs是什么,并试图总结近20年来以MTBC中CRISPR位点的遗传多样性为视角研究新模型所取得的研究成果。我们表明,借助“间隔寡核苷酸分型”对CRISPR序列多样性的研究,在我们对MTBC群体结构的整体理解中发挥了重要作用。

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