z-logo
Premium
Gene silencing by H‐NS from distal DNA site
Author(s) -
Shin Minsang,
Lagda Arvin Cesar,
Lee Jae Woong,
Bhat Abhay,
Rhee Joon Haeng,
Kim JeongSun,
Takeyasu Kunio,
Choy Hyon E.
Publication year - 2012
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/mmi.12012
Subject(s) - biology , nucleoid , rna polymerase , transcription (linguistics) , promoter , dna , microbiology and biotechnology , dna binding protein , gene , transcription factor , escherichia coli , genetics , gene expression , linguistics , philosophy
Summary 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 ( LEE5 p ) 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 LEE5 p 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 α subunit of RNAP , which prevents the processing of RNAP –promoter complexes into initiation‐competent open promoter complexes, thereby regulating LEE5 p from distance.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom