SREBP-1 as a transcriptional integrator of circadian and nutritional cues in the liver

被引:68
作者
Brewer, M
Lange, D
Baler, R
Anzulovich, A
机构
[1] NIMH, Unit Temporal Gene Express, Lab Cellular & Mol Regulat, NIH, Bethesda, MD 20892 USA
[2] NINDS, Intramural Informat Technol Program, NIH, Bethesda, MD 20892 USA
关键词
circadian; liver; sterol response element binding protein; feeding behavior;
D O I
10.1177/0748730405275952
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The act of feeding in mammals can generate such powerful cues for peripheral organs that, under certain conditions, they can override the entraining signals coming from the clock in the brain. Restricting the feeding time to the inactivity period, for example, can completely and quickly reverse the rhythms of gene expression in the liver. This manipulation does not affect the central oscillator in the suprachiasmatic nucleus, which is phase-locked to the light-dark cycle, but does release the peripheral oscillations in the liver from central control. It seems reasonable to predict the existence of one or more immediate response systems designed to sense the need to acutely reverse the sequence of absorptive and postabsorptive phases in the liver. In this study, the authors monitored the posttranslational activation of the sterol response element binding proteins from a circadian point of view to evaluate the role they might play in the circadian organization of the liver transcriptome as well as in the reversal of hepatic physiology that accompanies diurnal restricted feeding. This study highlights a possible direct link between the immediate effects of food consumption on the level of key membrane and humoral factors and the expression status of a set of coordinately regulated target genes in the liver.
引用
收藏
页码:195 / 205
页数:11
相关论文
共 41 条
[21]   RAPID SWITCH OF HEPATIC FATTY-ACID METABOLISM FROM OXIDATION TO ESTERIFICATION DURING DIURNAL FEEDING OF MEAL-FED RATS CORRELATES WITH CHANGES IN THE PROPERTIES OF ACETYL-COA CARBOXYLASE, BUT NOT OF CARNITINE PALMITOYLTRANSFERASE-I [J].
MOIR, AMB ;
ZAMMIT, VA .
BIOCHEMICAL JOURNAL, 1993, 291 :241-246
[22]   Circadian transcription -: Thinking outside the E-Box [J].
Muñoz, E ;
Brewer, M ;
Baler, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (39) :36009-36017
[23]   STRUCTURE AND FUNCTION OF HELIX-LOOP-HELIX PROTEINS [J].
MURRE, C ;
BAIN, G ;
VANDIJK, MA ;
ENGEL, I ;
FURNARI, BA ;
MASSARI, ME ;
MATTHEWS, JR ;
QUONG, MW ;
RIVERA, RR ;
STUIVER, MH .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1994, 1218 (02) :129-135
[24]   Sterol regulatory element-binding proteins (SREBPs): Key regulators of nutritional homeostasis and insulin action [J].
Osborne, TF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (42) :32379-32382
[25]   Differential stimulation of cholesterol and unsaturated fatty acid biosynthesis in cells expressing individual nuclear sterol regulatory element-binding proteins [J].
Pai, JT ;
Guryev, O ;
Brown, MS ;
Goldstein, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) :26138-26148
[26]   Coordinated transcription of key pathways in the mouse by the circadian clock [J].
Panda, S ;
Antoch, MP ;
Miller, BH ;
Su, AI ;
Schook, AB ;
Straume, M ;
Schultz, PG ;
Kay, SA ;
Takahashi, JS ;
Hogenesch, JB .
CELL, 2002, 109 (03) :307-320
[27]  
Patel DD, 2001, J LIPID RES, V42, P328
[28]   Evidence for a circadian rhythm of insulin release from perifused rat pancreatic islets [J].
Peschke, E ;
Peschke, D .
DIABETOLOGIA, 1998, 41 (09) :1085-1092
[29]   CLONING AND CHARACTERIZATION OF THE EPSILON-ISOFORM AND ZETA-ISOFORM OF THE 14-3-3-PROTEINS [J].
ROSEBOOM, PH ;
WELLER, JL ;
BABILA, T ;
AITKEN, A ;
SELLERS, LA ;
MOFFETT, JR ;
NAMBOODIRI, MAA ;
KLEIN, DC .
DNA AND CELL BIOLOGY, 1994, 13 (06) :629-640
[30]   METABOLIC FUEL HOMEOSTASIS IN SYRIAN-HAMSTERS - NYCTHEMERAL AND EXERCISE VARIABLES [J].
ROWLAND, N .
PHYSIOLOGY & BEHAVIOR, 1984, 33 (02) :243-252