Termination factor Rho and its cofactors NusA and NusG silence foreign DNA in E-coli

被引:243
作者
Cardinale, Christopher J. [2 ]
Washburn, Robert S. [1 ]
Tadigotla, Vasisht R. [3 ]
Brown, Lewis M. [4 ]
Gottesman, Max E. [1 ,5 ]
Nudler, Evgeny [2 ]
机构
[1] Columbia Univ, Med Ctr, Dept Microbiol, New York, NY 10032 USA
[2] NYU, Sch Med, Dept Biochem, New York, NY 10016 USA
[3] Rutgers State Univ, BioMaPS Inst Quantitat Biol, Piscataway, NJ 08854 USA
[4] Columbia Univ, Comparat Proteom Ctr, Dept Biol Sci, New York, NY 10027 USA
[5] Columbia Univ, Med Ctr, Dept Biochem & Mol Biophys, New York, NY 10032 USA
关键词
D O I
10.1126/science.1152763
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transcription of the bacterial genome by the RNA polymerase must terminate at specific points. Transcription can be terminated by Rho factor, an essential protein in enterobacteria. We used the antibiotic bicyclomycin, which inhibits Rho, to assess its role on a genome-wide scale. Rho is revealed as a global regulator of gene expression that matches Escherichia coli transcription to translational needs. We also found that genes in E. coli that are most repressed by Rho are prophages and other horizontally acquired portions of the genome. Elimination of these foreign DNA elements increases resistance to bicyclomycin. Although rho remains essential, such reduced-genome bacteria no longer require Rho cofactors NusA and NusG. Deletion of the cryptic rac prophage in wild-type E. coli increases bicyclomycin resistance and permits deletion of nusG. Thus, Rho termination, supported by NusA and NusG, is required to suppress the toxic activity of foreign genes.
引用
收藏
页码:935 / 938
页数:4
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