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McrB(S)参与大肠杆菌K-12中McrBC限制作用的证据。

Evidence of participation of McrB(S) in McrBC restriction in Escherichia coli K-12.

作者信息

Beary T P, Braymer H D, Achberger E C

机构信息

Department of Biological Sciences, Nicholls State University, Thibodaux, Louisiana 70310, USA.

出版信息

J Bacteriol. 1997 Dec;179(24):7768-75. doi: 10.1128/jb.179.24.7768-7775.1997.

Abstract

The McrBC restriction system has the ability to restrict DNA containing 5-hydroxymethylcytosine, N4-methylcytosine, and 5-methylcytosine at specific sequences. The mcrB gene produces two gene products. The complete mcrB open reading frame produces a 51-kDa protein (McrB(L)) and a 33-kDa protein (McrB(S)). The smaller McrB polypeptide is produced from an in-frame, internal translational start site in the mcrB gene. The McrB(S) sequence is identical to that of McrB(L) except that it lacks 161 amino acids present at the N-terminal end of the latter protein. It has been suggested that McrB(L) is the DNA binding restriction subunit. The function of McrB(S) is unknown, although there has been speculation that it plays some role in the modulation of McrBC restriction. Studies of the function of McrB(S) have been challenging since it is produced in frame with McrB(L). In this study, we tested the effects of underproduction (via antisense RNA) and overproduction (via gene dosage) of mcrBC gene products on restriction levels of the mcrBC+ strain JM107. Among the parameters monitored was the induction of SOS responses, which indicate of DNA damage. Evidence from this study suggests that McrB(S) is necessary for stabilization of the McrBC restriction complex in vivo.

摘要

McrBC限制系统能够在特定序列处限制含有5-羟甲基胞嘧啶、N4-甲基胞嘧啶和5-甲基胞嘧啶的DNA。mcrB基因产生两种基因产物。完整的mcrB开放阅读框产生一种51 kDa的蛋白质(McrB(L))和一种33 kDa的蛋白质(McrB(S))。较小的McrB多肽由mcrB基因中的一个框内内部翻译起始位点产生。McrB(S)的序列与McrB(L)的序列相同,只是它缺少后者蛋白质N末端存在的161个氨基酸。有人提出McrB(L)是DNA结合限制亚基。McrB(S)的功能尚不清楚,尽管有人推测它在McrBC限制的调节中起某种作用。由于McrB(S)与McrB(L)是框内产生的,对其功能的研究一直具有挑战性。在本研究中,我们测试了mcrBC基因产物的低表达(通过反义RNA)和高表达(通过基因剂量)对mcrBC+菌株JM107限制水平的影响。监测的参数之一是SOS反应的诱导,这表明存在DNA损伤。本研究的证据表明,McrB(S)对于体内McrBC限制复合物的稳定是必需的。

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