| Literature DB >> 30954403 |
Bin Wang1, Arminja N Kettenbach2, Xiaoying Zhou1, Jennifer J Loros3, Jay C Dunlap4.
Abstract
In the negative feedback loop driving fungal and animal circadian oscillators, negative elements (FREQUENCY [FRQ], PERIODS [PERs], and CRYPTOCHROMES [CRYs]) are understood to inhibit their own expression, in part by promoting the phosphorylation of their heterodimeric transcriptional activators (e.g., White Collar-1 [WC-1]-WC-2 [White Collar complex; WCC] and BMAL1/Circadian Locomotor Output Cycles Kaput [CLOCK]). However, correlations between heterodimer activity and phosphorylation are weak, contradictions exist, and mechanistic details are almost wholly lacking. We report mapping of 80 phosphosites on WC-1 and 15 on WC-2 and elucidation of the time-of-day-specific code, requiring both a group of phosphoevents on WC-1 and two distinct clusters on WC-2, that governs circadian repression, leading to feedback loop closure. Combinatorial control via phosphorylation also governs rhythmic WCC binding to the promoters of clock-controlled genes mediating the essential first step in circadian output, a group encoding both transcription factors and signaling proteins. These data provide a basic mechanistic understanding for fundamental events underlying circadian negative feedback and output, key aspects of circadian biology.Entities:
Keywords: C-box; DNA binding; FRQ; WC-1; WC-2; ccgs; clock-controlled genes; feedback loop; frq transcription; phosphorylation
Mesh:
Substances:
Year: 2019 PMID: 30954403 PMCID: PMC6583785 DOI: 10.1016/j.molcel.2019.03.003
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970