Transcriptional activator C protein-mediated unwinding of DNA as a possible mechanism for mom gene activation

被引:11
作者
Basak, S [1 ]
Nagaraja, V [1 ]
机构
[1] Indian Inst Sci, Dept Microbiol & Cell Biol, Bangalore 560012, Karnataka, India
关键词
bacteriophage Mu; mom; C protein; DNA distortion;
D O I
10.1006/jmbi.1998.2213
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The bacteriophage Mu mom gene encodes the unique DNA-modification function of the phage. Regulation of the mom gene at the transcriptional level is brought about by the transactivator protein C of the phage. The morn promoter is an activator-dependent weak promoter having poor -10 and -35 elements separated by a 19 bp suboptimal spacer region. These features could constrain RNA polymerase occupancy at the promoter. Here, we have probed into the mechanism by which C protein acts as a transcriptional activator at P-mom. In vivo dimethyl sulfate footprinting studies demonstrate C protein-mediated asymmetric distortion of its specific site at the mom regulatory region. Using a coupled topoisomerase assay, we demonstrate that C protein induces the unwinding of DNA. This C-mediated unwinding seems to be localised to the 3' flanking region of the C binding site located adjacent to and overlapping the -35 element of P-mom. These results suggest that C protein-mediated torsional changes could be reorienting, the -10 and -35 elements to a favorable conformation for RNA polymerase occupancy at the mom promoter. (C) 1998 Academic Press.
引用
收藏
页码:893 / 902
页数:10
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