Gene silencing by H-NS from distal DNA site

被引:25
|
作者
Shin, Minsang [1 ,2 ,5 ]
Lagda, Arvin Cesar [1 ,2 ]
Lee, Jae Woong [1 ,2 ]
Bhat, Abhay [1 ,2 ]
Rhee, Joon Haeng [2 ]
Kim, Jeong-Sun [3 ,4 ]
Takeyasu, Kunio [5 ]
Choy, Hyon E. [1 ,2 ]
机构
[1] Ctr Host Def Enteropathogen Bacteria Infect, Kwangju 501746, South Korea
[2] Chonnam Natl Univ, Sch Med, Dept Microbiol, Kwangju 501746, South Korea
[3] Chonnam Natl Univ, Dept Chem, Kwangju 500757, South Korea
[4] Chonnam Natl Univ, Inst Basic Sci, Kwangju 500757, South Korea
[5] Kyoto Univ, Grad Sch Biostudies, Lab Plasma Membrane & Nucl Signaling, Sakyo Ku, Kyoto 6068501, Japan
关键词
POLYMERASE-ALPHA-SUBUNIT; ENTEROPATHOGENIC ESCHERICHIA-COLI; CATABOLITE ACTIVATOR PROTEIN; NUCLEOID-ASSOCIATED PROTEIN; C-TERMINAL DOMAIN; RNA-POLYMERASE; TRANSCRIPTION ACTIVATION; PROMOTER RECOGNITION; COOPERATIVE BINDING; STRUCTURAL BASIS;
D O I
10.1111/mmi.12012
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
In the modern concept of gene regulation, DNA looping is the most common underlying mechanism in the interaction between RNA polymerase (RNAP) and transcription factors acting at a distance. This study demonstrates an additional mechanism by which DNA-bound proteins communicate with each other, by analysing the bacterial histone-like nucleoid-structuring protein (H-NS), a general transcriptional silencer. The LEE5 promoter (LEE5p) of enteropathogenic Escherichia coli was used as a model system to investigate the mechanism of H-NS-mediated transcription repression. We found that H-NS represses LEE5p by binding to a cluster of A tracks upstream of -114, followed by spreading to a site at the promoter through the oligomerization of H-NS molecules. At the promoter, the H-NS makes a specific contact with the carboxy terminal domain of the a subunit of RNAP, which prevents the processing of RNAPpromoter complexes into initiation-competent open promoter complexes, thereby regulating LEE5p from distance.
引用
收藏
页码:707 / 719
页数:13
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