Nakashima Ayumu, Kawamoto Takeshi, Honda Kiyomasa K, Ueshima Taichi, Noshiro Mitsuhide, Iwata Tomoyuki, Fujimoto Katsumi, Kubo Hiroshi, Honma Sato, Yorioka Noriaki, Kohno Nobuoki, Kato Yukio
Department of Dental and Medical Biochemistry, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima 734-8553, Japan.
Mol Cell Biol. 2008 Jun;28(12):4080-92. doi: 10.1128/MCB.02168-07. Epub 2008 Apr 14.
DEC1 suppresses CLOCK/BMAL1-enhanced promoter activity, but its role in the circadian system of mammals remains unclear. Here we examined the effect of Dec1 overexpression or deficiency on circadian gene expression triggered with 50% serum. Overexpression of Dec1 delayed the phase of clock genes such as Dec1, Dec2, Per1, and Dbp that contain E boxes in their regulatory regions, whereas it had little effect on the circadian phase of Per2 and Cry1 carrying CACGTT E' boxes. In contrast, Dec1 deficiency advanced the phase of the E-box-containing clock genes but not that of the E'-box-containing clock genes. Accordingly, DEC1 showed strong binding and transrepression on the E box, but not on the E' box, in chromatin immunoprecipitation, electrophoretic mobility shift, and luciferase reporter assays. Dec1-/- mice showed behavioral rhythms with slightly but significantly longer circadian periods under conditions of constant darkness and faster reentrainment to a 6-h phase-advanced shift of a light-dark cycle. Knockdown of Dec2 with small interfering RNA advanced the phase of Dec1 and Dbp expression, and double knockdown of Dec1 and Dec2 had much stronger effects on the expression of the E-box-containing clock genes. These findings suggest that DEC1, along with DEC2, plays a role in the finer regulation and robustness of the molecular clock.
DEC1可抑制CLOCK/BMAL1增强的启动子活性,但其在哺乳动物昼夜节律系统中的作用仍不清楚。在此,我们研究了Dec1过表达或缺失对50%血清引发的昼夜节律基因表达的影响。Dec1的过表达延迟了Dec1、Dec2、Per1和Dbp等在其调控区域含有E盒的生物钟基因的相位,而对携带CACGTT E'盒的Per2和Cry1的昼夜节律相位影响不大。相反,Dec1缺失使含有E盒的生物钟基因的相位提前,但不影响含有E'盒的生物钟基因的相位。因此,在染色质免疫沉淀、电泳迁移率变动和荧光素酶报告基因检测中,DEC1在E盒上显示出强结合和反式抑制作用,但在E'盒上没有。在持续黑暗条件下,Dec1-/-小鼠表现出行为节律,其昼夜周期略长但显著延长,并且对明暗周期提前6小时的相位移动重新同步更快。用小干扰RNA敲低Dec2可使Dec1和Dbp表达的相位提前,同时敲低Dec1和Dec2对含有E盒的生物钟基因的表达有更强的影响。这些发现表明,DEC1与DEC2一起在分子钟的精细调节和稳健性中发挥作用。