Kawamoto Takeshi, Noshiro Mitsuhide, Sato Fuyuki, Maemura Koji, Takeda Norihiko, Nagai Ryozo, Iwata Tomoyuki, Fujimoto Katsumi, Furukawa Masae, Miyazaki Kazuko, Honma Sato, Honma Ken ichi, Kato Yukio
Department of Dental and Medical Biochemistry, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima 734-8553, Japan.
Biochem Biophys Res Commun. 2004 Jan 2;313(1):117-24. doi: 10.1016/j.bbrc.2003.11.099.
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.
与生物钟基因Per转录相关的自反馈环通常被认为是昼夜节律产生的分子机制,其中CLOCK/BMAL作为正向调节因子,而PER/CRY作为负向调节因子。我们在此展示了一个编码碱性螺旋-环-螺旋转录因子的Dec1的自反馈环:CLOCK/BMAL增强了Dec1的启动子活性,而DEC1和DEC2以及PER和CRY抑制了诱导表达。三个CACGTG E盒负责Dec1转录的激活和抑制。Clock/Bmal的强制表达增加了内源性Dec1 mRNA水平,而Dec1的过表达导致Dec2、Per2和Dbp表达的抑制。Clock/Clock突变小鼠心脏中的Dec1表达水平在一整天内持续较低。这些发现表明,Dec1受CLOCK/BMAL正向调节,并通过抑制CLOCK/BMAL诱导的基因表达参与昼夜节律调节。在某些情况下,Dec1的自反馈环可能与Per的核心反馈环相互连锁。