Bétermier M, Poquet I, Alazard R, Chandler M
Molecular Genetics and Microbiology Laboratory, Centre National de la Recherche Scientifique UPR 9007, Toulouse, France.
J Bacteriol. 1993 Jun;175(12):3798-811. doi: 10.1128/jb.175.12.3798-3811.1993.
The Escherichia coli FIS (factor for inversion stimulation) protein has been implicated in assisting bacteriophage Mu repressor, c, in maintaining the lysogenic state under certain conditions. In a fis strain, a temperature-inducible Mucts62 prophage is induced at lower temperatures than in a wild-type host (M. Bétermier, V. Lefrère, C. Koch, R. Alazard, and M. Chandler, Mol. Microbiol. 3:459-468, 1989). Increasing the prophage copy number rendered Mucts62 less sensitive to this effect of the fis mutation, which thus seems to depend critically on the level of repressor activity. The present study also provides evidence that FIS affects the control of Mu gene expression and transposition. As judged by the use of lac transcriptional fusions, repression of early transcription was reduced three- to fourfold in a fis background, and this could be compensated by an increase in cts62 gene copy number. c was also shown to inhibit Mu transposition two- to fourfold less strongly in a fis host. These modulatory effects, however, could not be correlated to sequence-specific binding of FIS to the Mu genome, in particular to the strong site previously identified on the left end. We therefore speculate that a more general function of FIS is responsible for the observed modulation of Mu lysogeny.
大肠杆菌FIS(反转刺激因子)蛋白在某些条件下参与协助噬菌体Mu阻遏物c维持溶原状态。在fis菌株中,温度诱导型Mucts62原噬菌体在比野生型宿主更低的温度下被诱导(M. 贝泰米尔、V. 勒弗雷尔、C. 科赫、R. 阿拉扎德和M. 钱德勒,《分子微生物学》3:459 - 468,1989年)。增加原噬菌体拷贝数使Mucts62对fis突变的这种效应不那么敏感,因此这似乎严重依赖于阻遏物活性水平。本研究还提供证据表明FIS影响Mu基因表达和转座的控制。通过使用lac转录融合判断,在fis背景下早期转录的抑制降低了三到四倍,这可以通过增加cts62基因拷贝数来补偿。还表明在fis宿主中,c抑制Mu转座的强度也降低了两到四倍。然而,这些调节作用与FIS与Mu基因组的序列特异性结合无关,特别是与先前在左端鉴定出的强位点无关。因此,我们推测FIS的一个更普遍的功能负责观察到的对Mu溶原性的调节。