The HP1α protein is mandatory to repress the circadian clock and its output genes during the 12 h period of transcriptional repression

Abstract

The transcriptional repressions driven by the circadian core clock repressors RevErbα, E4BP4, and CRY1/PER1 involve feedback loops which are mandatory for generating the circadian rhythms. These repressors are known to bind to cognate DNA binding sites, but how their circadian bindings trigger the cascade of events leading to these repressions remain to be elucidated. Through molecular and genetic analyses, we now demonstrate that the chromatin protein HP1α plays a key role in these transcriptional repressions of both the circadian clock (CC) genes and their cognate output genes (CCGs). We show that these CC repressors recruit the HP1α protein downstream from a repressive cascade, and that this recruitment is mandatory for the maintenance of both the CC integrity and the expression of the circadian genes. We further show that the presence of HP1α is critical for both the repressor-induced chromatin compaction and the generation of “transcriptionally repressed biomolecular hydrophobic condensates” and demonstrates that HP1α is mandatory within the CC output genes for both the recruitment of DNA methylating enzymes on the intronic deoxyCpG islands and their subsequent methylation.

The circadian demethylation of a unique intronic deoxymethylCpG-rich island boosts the transcription of its cognate circadian clock output gene

“…S1 C and D ) to its cognate-site, and iii) the removal of the HP1α protein ( Figs. 4 A and B and 2 A and B of our accompanying paper ( 59 ) entitled “ The HP1α protein is mandatory to repress the circadian clock and its output genes during the 12h period of transcriptional repression ”), all of which resulting in an increased activity of the DNA demethylating enzymes ( Fig. 1 D and E ).…”