YY1-controlled regulatory connectivity and transcription are influenced by the cell cycle.
Jessica C LamNicholas G AboredenSusannah C MidlaSiqing WangAnran HuangCheryl A KellerBelinda M GiardineKate A HendersonRoss Cameron HardisonHaoyue ZhangGerd A BlobelPublished in: Nature genetics (2024)
Few transcription factors have been examined for their direct roles in physically connecting enhancers and promoters. Here acute degradation of Yin Yang 1 (YY1) in erythroid cells revealed its requirement for the maintenance of numerous enhancer-promoter loops, but not compartments or domains. Despite its reported ability to interact with cohesin, the formation of YY1-dependent enhancer-promoter loops does not involve stalling of cohesin-mediated loop extrusion. Integrating mitosis-to-G1-phase dynamics, we observed partial retention of YY1 on mitotic chromatin, predominantly at gene promoters, followed by rapid rebinding during mitotic exit, coinciding with enhancer-promoter loop establishment. YY1 degradation during the mitosis-to-G1-phase interval revealed a set of enhancer-promoter loops that require YY1 for establishment during G1-phase entry but not for maintenance in interphase, suggesting that cell cycle stage influences YY1's architectural function. Thus, as revealed here for YY1, chromatin architectural functions of transcription factors can vary in their interplay with CTCF and cohesin as well as by cell cycle stage.
Keyphrases
- transcription factor
- cell cycle
- cell proliferation
- dna binding
- genome wide identification
- single cell
- dna methylation
- induced apoptosis
- liver failure
- dna damage
- functional connectivity
- signaling pathway
- binding protein
- resting state
- copy number
- endoplasmic reticulum stress
- hepatitis b virus
- drug induced
- sensitive detection