BRG1 Interacts with Nrf2 To Selectively Mediate HO-1 Induction in Response to Oxidative Stress
Author(s) -
Jianyong Zhang,
Tsutomu Ohta,
Atsushi Maruyama,
Tomonori Hosoya,
Keizo Nishikawa,
Jonathan Maher,
Shigeki Shibahara,
Ken Itoh,
Masayuki Yamamoto
Publication year - 2006
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00700-06
Subject(s) - biology , microbiology and biotechnology , chromatin immunoprecipitation , gene knockdown , gene , chromatin , promoter , gene expression , chromatin remodeling , regulation of gene expression , small interfering rna , rna , genetics
NF-E2-related factor 2 (Nrf2) regulates antioxidant-responsive element-mediated induction of cytoprotective genes in response to oxidative stress. The purpose of this study was to determine the role of BRG1, a catalytic subunit of SWI2/SNF2-like chromatin-remodeling complexes, in Nrf2-mediated gene expression. Small interfering RNA knockdown of BRG1 in SW480 cells selectively decreased inducible expression of the heme oxygenase 1 (HO-1 ) gene after diethylmaleate treatment but did not affect other Nrf2 target genes, such as the gene encoding NADPH:quinone oxidoreductase 1 (NQO1 ). Chromatin immunoprecipitation analysis revealed that Nrf2 recruits BRG1 to bothHO-1 andNQO1 regulatory regions. However, BRG1 knockdown selectively decreased the recruitment of RNA polymerase II to theHO-1 promoter but not to theNQO1 promoter.HO-1 , but not other Nrf2-regulated genes, harbors a sequence of TG repeats capable of forming Z-DNA with BRG1 assistance. Similarly, replacement of the TG repeats with an alternative Z-DNA-forming sequence led to BRG1-mediated activation ofHO-1 . These results thus demonstrate that BRG1, through the facilitation of Z-DNA formation and subsequent recruitment of RNA polymerase II, is critical in Nrf2-mediated inducible expression ofHO-1 .
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