Circadian regulation of cAMP response element-mediated gene expression in the Suprachiasmatic nuclei

被引:234
作者
Obrietan, K [1 ]
Impey, S [1 ]
Smith, D [1 ]
Athos, J [1 ]
Storm, DR [1 ]
机构
[1] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
关键词
D O I
10.1074/jbc.274.25.17748
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
A program of stringently-regulated gene expression is thought to be a fundamental component of the circadian clock Although recent work has implicated a role for E-box-dependent transcription in circadian rhythmicity, the contribution of other enhancer elements has yet to be assessed. Here, we report that cells of the supra-chiasmatic nuclei (SCN) exhibit a prominent circadian oscillation in cAMP response dement (CRE)-mediated gene expression. Maximal reporter gene expression occurred from late-subjective night to mid-subjective day. Cycling of CRE-dependent transcription was not observed in other brain regions, including the supraoptic nucleus and piriform cortex. Levels of the phospho-active form of the transcription factor CREB (P-CBEB) varied as a function of circadian time, peak P-CREB levels occurred during the mid- to late-subjective night. Furthermore, photic stimulation during the subjective might, but not during the subjective day, triggered a marked increase in CRE-mediated gene expression in the SCN. Reporter gene experiments showed that activation of the p44/42 mitogen-activated protein kinase signaling cascade is required for Ca2+-dependent stimulation of CRE-mediated transcription in the SCN. These findings reveal the CREB/CRE transcriptional pathway to be circadian-regulated within the SCN, and raise the possibility that this pathway provides signaling information essential for normal clock function.
引用
收藏
页码:17748 / 17756
页数:9
相关论文
共 74 条
[51]   Stimulation of growth factor receptor signal transduction by activation of voltage-sensitive calcium channels [J].
Rosen, LB ;
Greenberg, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (03) :1113-1118
[52]   MEMBRANE DEPOLARIZATION AND CALCIUM INFLUX STIMULATE MEK AND MAP KINASE VIA ACTIVATION OF RAS [J].
ROSEN, LB ;
GINTY, DD ;
WEBER, MJ ;
GREENBERG, ME .
NEURON, 1994, 12 (06) :1207-1221
[53]   LIGHT-PULSES THAT SHIFT RHYTHMS INDUCE GENE-EXPRESSION IN THE SUPRACHIASMATIC NUCLEUS [J].
RUSAK, B ;
ROBERTSON, HA ;
WISDEN, W ;
HUNT, SP .
SCIENCE, 1990, 248 (4960) :1237-1240
[54]   Calcium influx induces neurite growth through a Src-Ras signaling cassette [J].
Rusanescu, G ;
Qi, HQ ;
Thomas, SM ;
Brugge, JS ;
Halegoua, S .
NEURON, 1995, 15 (06) :1415-1425
[55]   CYCLE is a second bHLH-PAS clock protein essential for circadian rhythmicity and transcription of Drosophila period and timeless [J].
Rutila, JE ;
Suri, V ;
Le, M ;
So, WV ;
Rosbash, M ;
Hall, JC .
CELL, 1998, 93 (05) :805-814
[56]   INDUCTION OF PROTO-ONCOGENE FOS TRANSCRIPTION THROUGH THE ADENYLATE-CYCLASE PATHWAY - CHARACTERIZATION OF A CAMP-RESPONSIVE ELEMENT [J].
SASSONECORSI, P ;
VISVADER, J ;
FERLAND, L ;
MELLON, PL ;
VERMA, IM .
GENES & DEVELOPMENT, 1988, 2 (12A) :1529-1538
[57]   INVOLVEMENT OF THE CA2+-DEPENDENT PHOSPHATASE CALCINEURIN IN GENE-TRANSCRIPTION THAT BY STIMULATED BY CAMP THROUGH CAMP RESPONSE ELEMENTS [J].
SCHWANINGER, M ;
BLUME, R ;
KRUGER, M ;
LUX, G ;
OETJEN, E ;
KNEPEL, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (15) :8860-8866
[58]  
SEGER R, 1994, J BIOL CHEM, V269, P25699
[59]   LOSS OF CIRCADIAN BEHAVIORAL RHYTHMS AND PER RNA OSCILLATIONS IN THE DROSOPHILA MUTANT TIMELESS [J].
SEHGAL, A ;
PRICE, JL ;
MAN, B ;
YOUNG, MW .
SCIENCE, 1994, 263 (5153) :1603-1606
[60]   CREB - A CA2+-REGULATED TRANSCRIPTION FACTOR PHOSPHORYLATED BY CALMODULIN-DEPENDENT KINASES [J].
SHENG, M ;
THOMPSON, MA ;
GREENBERG, ME .
SCIENCE, 1991, 252 (5011) :1427-1430