Laboratory for Systems Biology, RIKEN Center for Developmental Biology, Chuo-ku, Kobe, Hyogo, Japan.
Cell. 2011 Jan 21;144(2):268-81. doi: 10.1016/j.cell.2010.12.019.
Direct evidence for the requirement of delay in feedback repression in the mammalian circadian clock has been elusive. Cryptochrome 1 (Cry1), an essential clock component, displays evening-time expression and serves as a strong repressor at morning-time elements (E box/E' box). In this study, we reveal that a combination of day-time elements (D box) within the Cry1-proximal promoter and night-time elements (RREs) within its intronic enhancer gives rise to evening-time expression. A synthetic composite promoter produced evening-time expression, which was further recapitulated by a simple phase-vector model. Of note, coordination of day-time with night-time elements can modulate the extent of phase delay. A genetic complementation assay in Cry1(-/-):Cry2(-/-) cells revealed that substantial delay of Cry1 expression is required to restore circadian rhythmicity, and its prolonged delay slows circadian oscillation. Taken together, our data suggest that phase delay in Cry1 transcription is required for mammalian clock function.
直接证据表明,哺乳动物生物钟的反馈抑制需要延迟。隐花色素 1(Cry1)是一个基本的生物钟成分,表现出夜间表达,并作为早晨元件(E 盒/E' 盒)的强抑制剂。在这项研究中,我们揭示了 Cry1 近端启动子内的日间元件(D 盒)和其内含子增强子内的夜间元件(RREs)的组合导致夜间表达。一个合成的复合启动子产生了夜间表达,这进一步被一个简单的相量模型所概括。值得注意的是,日间元件与夜间元件的协调可以调节相延迟的程度。在 Cry1(-/-):Cry2(-/-)细胞中的遗传互补测定表明,恢复生物钟节律需要大量延迟 Cry1 的表达,其延长的延迟会减缓生物钟的振荡。总的来说,我们的数据表明,Cry1 转录的相延迟是哺乳动物生物钟功能所必需的。