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Mu和IS1转座在大肠杆菌bgl位点表现出强烈的方向偏向性。

Mu and IS1 transpositions exhibit strong orientation bias at the Escherichia coli bgl locus.

作者信息

Manna D, Wang X, Higgins N P

机构信息

Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

J Bacteriol. 2001 Jun;183(11):3328-35. doi: 10.1128/JB.183.11.3328-3335.2001.

Abstract

The region upstream of the Escherichia coli bgl operon is an insertion hot spot for several transposons. Elements as distantly related as Tn1, Tn5, and phage Mu home in on this location. To see what characteristics result in a high-affinity site for transposition, we compared in vivo and in vitro Mu transposition patterns near the bgl promoter. In vivo, Mu insertions were focused in two narrow zones of DNA near bgl, and both zones exhibited a striking orientation bias. Five hot spots upstream of the bgl cyclic AMP binding protein (CAP) binding site had Mu insertions exclusively with the phage oriented left to right relative to the direction of bgl transcription. One hot spot within the CAP binding domain had the opposite (right-to-left) orientation of phage insertion. The DNA segment lying between these two Mu hot-spot clusters is extremely A/T rich (80%) and is an efficient target for insertion sequences during stationary phase. IS1 insertions that activate the bgl operon resulted in a decrease in Mu insertions near the CAP binding site. Mu transposition in vitro differed significantly from the in vivo transposition pattern, having a new hot-spot cluster at the border of the A/T-rich segment. Transposon hot-spot behavior and orientation bias may relate to an asymmetry of transposon DNA-protein complexes and to interactions with proteins that produce transcriptionally silenced chromatin.

摘要

大肠杆菌bgl操纵子上游区域是多个转座子的插入热点。诸如Tn1、Tn5和噬菌体Mu等亲缘关系甚远的元件都定位于此位置。为了探究何种特征导致了一个高亲和力的转座位点,我们比较了bgl启动子附近的体内和体外Mu转座模式。在体内,Mu插入集中在bgl附近的两个狭窄DNA区域,且这两个区域都表现出显著的方向偏向性。bgl环腺苷酸结合蛋白(CAP)结合位点上游的五个热点只有噬菌体相对于bgl转录方向从左到右定向时才有Mu插入。CAP结合域内的一个热点有相反(从右到左)的噬菌体插入方向。位于这两个Mu热点簇之间的DNA片段富含A/T(80%),并且在稳定期是插入序列的有效靶标。激活bgl操纵子的IS1插入导致CAP结合位点附近的Mu插入减少。体外Mu转座与体内转座模式显著不同,在富含A/T片段的边界有一个新的热点簇。转座子热点行为和方向偏向性可能与转座子DNA-蛋白质复合物的不对称性以及与产生转录沉默染色质的蛋白质的相互作用有关。

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