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IS608单链转座机制的体外重建

In vitro reconstitution of a single-stranded transposition mechanism of IS608.

作者信息

Guynet Catherine, Hickman Alison Burgess, Barabas Orsolya, Dyda Fred, Chandler Michael, Ton-Hoang Bao

机构信息

Laboratoire de Microbiologie et Génétique Moléculaires, CNRS UMR5100, 118 Rte de Narbonne, F31062 Toulouse Cedex, France.

出版信息

Mol Cell. 2008 Feb 15;29(3):302-12. doi: 10.1016/j.molcel.2007.12.008.

Abstract

Bacterial insertion sequences (IS) play an important role in restructuring their host genomes. IS608, from Helicobacter pylori, belongs to a newly recognized and widespread IS group with a unique transposition mechanism. We have reconstituted the entire set of transposition cleavage and strand transfer reactions in vitro and find that, unlike any other known transposition system, they strictly require single-strand DNA. TnpA, the shortest identified transposase, uses a nucleophilic tyrosine for these reactions. It recognizes and cleaves only the IS608 "top strand." The results support a transposition model involving excision of a single-strand circle with abutted left (LE) and right (RE) IS ends. Insertion occurs site specifically 3' to conserved and essential TTAC tetranucleotide and appears to be driven by LE. This single-strand transposition mode has important implications not only for dispersion of IS608 but also for the other members of this very large IS family.

摘要

细菌插入序列(IS)在其宿主基因组重组中发挥着重要作用。来自幽门螺杆菌的IS608属于一个新认识的且广泛存在的IS家族,具有独特的转座机制。我们在体外重建了整个转座切割和链转移反应体系,发现与任何其他已知的转座系统不同,它们严格需要单链DNA。已鉴定出的最短转座酶TnpA在这些反应中使用亲核酪氨酸。它仅识别并切割IS608的“顶链”。这些结果支持了一种转座模型,该模型涉及切除一个具有相邻左(LE)和右(RE)IS末端的单链环。插入位点特异性地位于保守且必需的TTAC四核苷酸的3'端,并且似乎由LE驱动。这种单链转座模式不仅对IS608的扩散具有重要意义,而且对这个非常大的IS家族的其他成员也具有重要意义。

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