Complexes containing activating transcription factor (ATF)/cAMP-responsive-element-binding protein (CREB) interact with the CCAAT enhancer-binding protein (C/EBP)-ATF composite site to regulate Gadd153 expression during the stress response

被引:394
作者
Fawcett, TW
Martindale, JL
Guyton, KZ
Hai, T
Holbrook, NJ
机构
[1] NIA, Gene Express & Aging Sect, Biol Chem Lab, NIH, Baltimore, MD 21224 USA
[2] Ohio State Univ, Dept Med Biochem, Ohio State Biochem Program, Columbus, OH 43210 USA
[3] Ohio State Univ, Neurobiotechnol Ctr, Columbus, OH 43210 USA
关键词
GADD153; protein; gene regulation; stress response; transcription factors;
D O I
10.1042/0264-6021:3390135
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
Gadd153, also known as chop, encodes a member of the CCAAT/enhancer-binding protein (C/EBP) transcription factor family and is transcriptionally activated by cellular stress signals. We recently demonstrated that arsenite treatment of rat pheochromocytoma PC12 cells results in the biphasic induction of Gadd153 mRNA expression, controlled in part through binding of C/EBP beta and two uncharacterized protein complexes to the C/EBP-ATF (activating transcription factor) composite site in the Gadd153 promoter. In this report, we identified components of these additional complexes as two ATF/CREB (cAMP-responsive-element-binding protein) transcription factors having differential binding activities dependent upon the time of arsenite exposure, During arsenite treatment of PC12 cells, we observed enhanced binding of ATF4 to the C/EBP-ATF site at 2 h as Gadd153 mRNA levels increased, and enhanced binding of ATF3 complexes at 6 h as Gadd153 expression declined. We further demonstrated that ATF4 activates, while ATF3 represses, Gadd153 promoter activity through the C/EBP-ATF site. ATF3 also repressed ATF4-mediated transactivation and arsenite-induced activation of the Gadd153 promoter. Our results suggest that numerous members of the ATF/CREB family are involved in the cellular stress response, and that regulation of stress-induced biphasic Gadd153 expression in PC12 cells involves the ordered, sequential binding of multiple transcription factor complexes to the C/EBP-ATF composite site.
引用
收藏
页码:135 / 141
页数:7
相关论文
共 57 条
[1]  
AVITAHL N, 1994, J BIOL CHEM, V269, P23553
[2]   CHOP (GADD153) AND ITS ONCOGENIC VARIANT, TLS-CHOP, HAVE OPPOSING EFFECTS ON THE INDUCTION OF G(1)/S ARREST [J].
BARONE, MV ;
CROZAT, A ;
TABAEE, A ;
PHILIPSON, L ;
RON, D .
GENES & DEVELOPMENT, 1994, 8 (04) :453-464
[3]  
BARTLETT JD, 1992, J BIOL CHEM, V267, P20465
[4]   INHIBITION OF ADIPOGENESIS BY THE STRESS-INDUCED PROTEIN CHOP (GADD153) [J].
BATCHVAROVA, N ;
WANG, XZ ;
RON, D .
EMBO JOURNAL, 1995, 14 (19) :4654-4661
[5]   DIFFERENT BINDING SPECIFICITIES AND TRANSACTIVATION OF VARIANT CRES BY CREB COMPLEXES [J].
BENBROOK, DM ;
JONES, NC .
NUCLEIC ACIDS RESEARCH, 1994, 22 (08) :1463-1469
[6]   Amino acid limitation induces expression of CHOP, a CCAAT/enhancer binding protein-related gene, at both transcriptional and post-transcriptional levels [J].
Bruhat, A ;
Jousse, C ;
Wang, XZ ;
Ron, D ;
Ferrara, M ;
Fafournoux, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (28) :17588-17593
[7]   Coordinate transactivation of the interleukin-2 CD28 response element by c-Rel and ATF-1/CREB2 [J].
Butscher, WG ;
Powers, C ;
Olive, M ;
Vinson, C ;
Gardner, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :552-560
[8]   REGULATION OF THE C/EBP-RELATED GENE GADD153 BY GLUCOSE DEPRIVATION [J].
CARLSON, SG ;
FAWCETT, TW ;
BARTLETT, JD ;
BERNIER, M ;
HOLBROOK, NJ .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (08) :4736-4744
[9]   Analysis of ATF3, a transcription factor induced by physiological stresses and modulated by gadd153/Chop10 [J].
Chen, BPC ;
Wolfgang, CD ;
Hai, TW .
MOLECULAR AND CELLULAR BIOLOGY, 1996, 16 (03) :1157-1168
[10]   PROTEIN-INTERACTION CLONING IN YEAST - IDENTIFICATION OF MAMMALIAN PROTEINS THAT REACT WITH THE LEUCINE ZIPPER OF JUN [J].
CHEVRAY, PM ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :5789-5793