Model-driven experimental approach reveals the complex regulatory distribution of p53 by the circadian factor Period 2.
Ontology highlight
ABSTRACT: The circadian clock and cell cycle networks are interlocked on the molecular level, with the core clock loop exerting a multilevel regulatory role over cell cycle components. This is particularly relevant to the circadian factor Period 2 (Per2), which modulates the stability of the tumor suppressor p53 in unstressed cells and transcriptional activity in response to genotoxic stress. Per2 binding prevents Mdm2-mediated ubiquitination of p53 and, therefore, its degradation, and oscillations in the peaks of Per2 and p53 were expected to correspond. However, our findings showed that Per2 and p53 rhythms were significantly out-of-phase relative to each other in cell lysates and in purified cytoplasmic fractions. These seemingly conflicting experimental data motivated the use of a combined theor
SUBMITTER: Gotoh T
PROVIDER: S-EPMC5127372 | biostudies-literature | 2016 Nov
REPOSITORIES: biostudies-literature
ACCESS DATA