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噬菌体Mu DNA的精确切除

Precise excision of bacteriophage Mu DNA.

作者信息

Abbes C, Sezonov G, Joseleau-Petit D, D'Ari R, Liébart J C

机构信息

Institut Jacques Monod, Centre National de la Recherche Scientifique (CNRS), Université Paris 6, Université Paris 7, France.

出版信息

Can J Microbiol. 2001 Aug;47(8):722-6.

Abstract

The temperate bacteriophage Mu is a transposable element that can integrate randomly into bacterial DNA, thereby creating mutations. Mutants due to an integrated Mu prophage do not give rise to revertants, as if Mu, unlike other transposable elements, were unable to excise precisely. In the present work, starting with a lacZ::Muc62(Ts) strain unable to form Lac+ colonies, we cloned a lacZ+ gene in vivo on a mini-Mu plasmid, under conditions of prophage induction. In all lac+ plasmids recovered, the wild-type sequence was restored in the region where the Mu prophage had been integrated. The recovery of lacZ+ genes shows that precise excision of Mu does indeed take place; the absence of Lac+ colonies suggests that precise excision events are systematically associated with loss of colony-forming ability.

摘要

温和噬菌体Mu是一种可转座元件,它能随机整合到细菌DNA中,从而产生突变。由于整合的Mu原噬菌体而产生的突变体不会产生回复体,就好像Mu与其他可转座元件不同,无法精确切除。在本研究中,我们从一个不能形成Lac⁺菌落的lacZ::Muc62(Ts)菌株开始,在原噬菌体诱导条件下,在体内将一个lacZ⁺基因克隆到一个微型Mu质粒上。在所有回收的lac⁺质粒中,Mu原噬菌体整合区域的野生型序列得以恢复。lacZ⁺基因的回收表明Mu确实发生了精确切除;没有Lac⁺菌落表明精确切除事件与菌落形成能力的丧失系统性相关。

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