Stress-induced stimulation of pituitary POMC gene expression is associated with activation of transcription factor AP-1 in hypothalamus and pituitary

被引:18
作者
Autelitano, DJ [1 ]
机构
[1] Baker Med Res Inst, Mol Physiol Lab, Prahran, Vic 3181, Australia
关键词
c-fos; c-jun; jun-B; restraint; proopiomelanocortin;
D O I
10.1016/S0361-9230(97)00303-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The response to environmental stimuli such as stress involves changes in gene transcription in both brain and pituitary, which in turn, facilitate adaptive phenotypic alterations favoring survival. In the present study we have examined the expression of the inducible immediate-early genes of the fos and jun families, and the activity of transcription factor AP-1 in the hypothalamus and anterior pituitary gland of rats, after a single restraint challenge. Restraint led to a rapid transient increase in c-fos but not c-jun expression in hypothalamus and pituitary. Changes in jun-B expression in hypothalamus were qualitatively similar to c-fos, though not statistically significant at 30 min, Furthermore, a single episode of restraint stress led to significant increases (50-100%) in nuclear AP-1 DNA binding activity in both hypothalamus and pituitary, while DNA binding of an unrelated transcription factor (Spl) was unchanged. Associated with the stress-induced activation of pituitary AP-I was a parallel three-to fourfold transcriptional stimulation of pituitary POMC gene expression, These data demonstrate that the rapidly inducible members of the fos and ion gene families contribute to increased activity of transcription factor AP-1 in both hypothalamus and pituitary following stress, and suggest that AP-1 may be a crucial factor involved in rapid transcriptional responses during stress. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:75 / 82
页数:8
相关论文
共 41 条
[11]   THE PROTOONCOGENE C-FOS IS INDUCED BY CORTICOTROPIN-RELEASING FACTOR AND STIMULATES PROOPIOMELANOCORTIN GENE-TRANSCRIPTION IN PITUITARY-CELLS [J].
BOUTILLIER, AL ;
SASSONECORSI, P ;
LOEFFLER, JP .
MOLECULAR ENDOCRINOLOGY, 1991, 5 (09) :1301-1310
[12]   EXPRESSION OF C-FOS IMMUNOREACTIVITY IN TRANSMITTER-CHARACTERIZED NEURONS AFTER STRESS [J].
CECCATELLI, S ;
VILLAR, MJ ;
GOLDSTEIN, M ;
HOKFELT, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (23) :9569-9573
[13]   FRA-1 - A SERUM-INDUCIBLE, CELLULAR IMMEDIATE-EARLY GENE THAT ENCODES A FOS-RELATED ANTIGEN [J].
COHEN, DR ;
CURRAN, T .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2063-2069
[14]   PATTERN AND TIME-COURSE OF IMMEDIATE-EARLY GENE-EXPRESSION IN RAT-BRAIN FOLLOWING ACUTE STRESS [J].
CULLINAN, WE ;
HERMAN, JP ;
BATTAGLIA, DF ;
AKIL, H ;
WATSON, SJ .
NEUROSCIENCE, 1995, 64 (02) :477-505
[15]  
CURRAN T, 1987, ONCOGENE, V2, P79
[16]   STRESS UPDATE - ADAPTATION OF THE HYPOTHALAMIC PITUITARY-ADRENAL AXIS TO CHRONIC STRESS [J].
DALLMAN, MF .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1993, 4 (02) :62-69
[17]   CONTROL OF EUKARYOTIC MESSENGER-RNA SYNTHESIS BY SEQUENCE-SPECIFIC DNA-BINDING PROTEINS [J].
DYNAN, WS ;
TJIAN, R .
NATURE, 1985, 316 (6031) :774-778
[18]  
GUARDIOLADIAZ HM, 1994, J BIOL CHEM, V269, P14784
[19]   CROSS-FAMILY DIMERIZATION OF TRANSCRIPTION FACTORS FOS JUN AND ATF CREB ALTERS DNA-BINDING SPECIFICITY [J].
HAI, T ;
CURRAN, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3720-3724
[20]   MUTUAL CROSS-MODULATION OF STEROID RETINOIC ACID RECEPTOR AND AP-1 TRANSCRIPTION FACTOR ACTIVITIES - A NOVEL PROPERTY WITH PRACTICAL IMPLICATIONS [J].
HERRLICH, P ;
PONTA, H .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1994, 5 (08) :341-346