| Literature DB >> 35273702 |
Zhao-Huan Zhang1,2, Jian-Mei Xiong3, Yun-Yi Zhu4, Xiao-Dan Zhang4, Wen-Jie Wu4, Lin Zhou2, Jian-Hua Zhuang5, Xiao-Hui Xu1,4.
Abstract
PER1 is a core component of the internal time-keeping system. In the suprachiasmatic nucleus, it serves as the primary circadian pacemaker in mammalian brains. PER1 functions with other clock components to generate a feedback loop involving the transcriptional repression of gene expression to produce a circadian rhythm with an approximately 24-hour cycle. Post-transcriptional modifications (PTMs) are a basic regulatory mechanism that both perpetuate self-sustained oscillations and interpret metabolic input into circadian physiology by affecting factors such as protein stability, interactions, localization, and activity. Here we examined whether the serine/threonine protein kinase WNK3, which is expressed in a circadian rhythm, can interact and colocalize with PER1 in the SCN. In rats, WNK3 knockdown in the SCN is associated with altered sleep patterns. Moreover, WNK3 can phosphorylate PER1 to promote its degradation and is associated with circadian oscillations when PER1 is expressed in vitro. AJTREntities:
Keywords: Circadian rhythm; PER1; SCN; WNK3; phosphorylation; sleep disorder
Year: 2022 PMID: 35273702 PMCID: PMC8902561
Source DB: PubMed Journal: Am J Transl Res ISSN: 1943-8141 Impact factor: 4.060