A novel autofeedback loop of Dec1 transcription involved in circadian rhythm regulation

被引:106
作者
Kawamoto, T
Noshiro, M
Sato, F
Maemura, K
Takeda, N
Nagai, R
Iwata, T
Fujimoto, K
Furukawa, M
Miyazaki, K
Honma, S
Honma, K
Kato, Y [1 ]
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Dept Dental & Med Biochem, Hiroshima 7348553, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Cardiovasc Med, Tokyo 1138655, Japan
[3] Hokkaido Univ, Grad Sch Med, Dept Physiol, Sapporo, Hokkaido 0608638, Japan
关键词
DEC1; circadian rhythm; clock; bHLH transcription factor;
D O I
10.1016/j.bbrc.2003.11.099
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
An autofeedback loop associated with transcription of clock gene(s), Per(s), is generally accepted as the molecular machinery of circadian rhythm generation, in which CLOCK/BMAL act as positive regulators and PER/CRY as negative ones. We show here an autofeedback loop of Dec1 encoding a basic helix-loop-helix transcription factor: CLOCK/BMAL increased the promoter activity of Dec1, and DEC1 and DEC2 as well as PERs and CRYs suppressed the induced expression. Three CACGTG E-boxes are responsible for both the activation and the suppression of Dec1 transcription. Forced expression of Clock/Bmal increased endogenous Dec1 mRNA level, and overexpression of Dec1 resulted in suppression of Dec2, Per2, and Dbp expression. The level of Dec1 expression in the heart of Clock/Clock mutant mice was continuously low throughout the day. These findings suggest that Dec1 is positively regulated by CLOCK/BMAL and is involved in circadian rhythm regulation by suppressing CLOCK/BMAL-induced gene expression. The autofeedback loop of Dec1 may be interlocked with the core feedback loop of Per in some situations. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:117 / 124
页数:8
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