SWI/SNF Regulates the Cellular Response to Hypoxia

被引:95
作者
Kenneth, Niall S. [1 ]
Mudie, Sharon [1 ]
van Uden, Patrick [1 ]
Rocha, Sonia [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Wellcome Trust Ctr Gene Regulat & Express, Dundee DD1 5EH, Scotland
关键词
NF-KAPPA-B; CHROMATIN-REMODELING COMPLEX; ARF TUMOR-SUPPRESSOR; GENE-EXPRESSION; INDUCIBLE FACTOR-1-ALPHA; PROTEASOMAL DEGRADATION; VASCULAR DEVELOPMENT; HIF-1-ALPHA; SUBUNIT; IDENTIFICATION;
D O I
10.1074/jbc.M808491200
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
Hypoxia induces a variety of cellular responses such as cell cycle arrest, apoptosis, and autophagy. Most of these responses are mediated by the hypoxia-inducible factor-1 alpha. To induce target genes, hypoxia-inducible factor-1 alpha requires a chromatin environment conducive to allow binding to specific sequences. Here, we have studied the role of the chromatin-remodeling complex SWI/SNF in the cellular response to hypoxia. We find that SWI/SNF is required for several of the cellular responses induced by hypoxia. Surprisingly, hypoxia-inducible factor-1 alpha is a direct target of the SWI/SNF chromatin-remodeling complex. SWI/SNF components are found associated with the hypoxia-inducible factor-1 alpha promoter and modulation of SWI/SNF levels results in pronounced changes in hypoxia-inducible factor-1 alpha expression and its ability to transactivate target genes. Furthermore, impairment of SWI/SNF function renders cells resistant to hypoxia-induced cell cycle arrest. These results reveal a previously uncharacterized dependence of hypoxia signaling on the SWI/SNF complex and demonstrate a new level of control over the hypoxia-inducible factor-1 alpha system.
引用
收藏
页码:4123 / 4131
页数:9
相关论文
共 49 条
[1]  
Abbott BD, 2000, DEV DYNAM, V219, P526, DOI 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1080>3.0.CO
[2]  
2-N
[3]   Negative and positive regulation of HIF-1:: A complex network [J].
Bárdos, JI ;
Ashcroft, M .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2005, 1755 (02) :107-120
[4]   Growth factor-mediated induction of HDM2 positively regulates hypoxia-inducible factor 1α expression [J].
Bárdos, JI ;
Chau, NM ;
Ashcroft, M .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (07) :2905-2914
[5]   HIF prolyl-hydroxylase 2 is the key oxygen sensor setting low steady-state levels of HIF-1α in normoxia [J].
Berra, E ;
Benizri, E ;
Ginouvès, A ;
Volmat, V ;
Roux, D ;
Pouysségur, J .
EMBO JOURNAL, 2003, 22 (16) :4082-4090
[6]  
Bruegge K, 2007, CURR MED CHEM, V14, P1853
[7]   Identification of novel small molecule inhibitors of hypoxia-inducible factor-1 that differentially block hypoxia-inducible factor-1 activity and hypoxia-inducible factor-1α induction in response to hypoxic stress and growth factors [J].
Chau, NM ;
Rogers, P ;
Aherne, W ;
Carroll, V ;
Collins, I ;
McDonald, E ;
Workman, P ;
Ashcroft, M .
CANCER RESEARCH, 2005, 65 (11) :4918-4928
[8]   Regulating SWI/SNF subunit levels via protein-protein interactions and proteasomal degradation: BAF155 and BAF170 limit expression of BAF57 [J].
Chen, JG ;
Archer, TK .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (20) :9016-9027
[9]   Reciprocal regulation of CD4/CD8 expression by SWI/SNF-like BAF complexes [J].
Chi, TH ;
Wan, M ;
Zhao, KJ ;
Taniuchi, I ;
Chen, L ;
Littman, DR ;
Crabtree, GR .
NATURE, 2002, 418 (6894) :195-199
[10]   Regulating cellular oxygen sensing by hydroxylation [J].
Fandrey, Joachim ;
Gorr, Thomas A. ;
Gassmann, Max .
CARDIOVASCULAR RESEARCH, 2006, 71 (04) :642-651