| Literature DB >> 35981542 |
Ioannis Sanidas1, Hanjun Lee2, Purva H Rumde1, Gaylor Boulay3, Robert Morris1, Gabriel Golczer1, Marcelo Stanzione1, Soroush Hajizadeh1, Jun Zhong1, Meagan B Ryan1, Ryan B Corcoran1, Benjamin J Drapkin4, Miguel N Rivera3, Nicholas J Dyson5, Michael S Lawrence6.
Abstract
The interaction of RB with chromatin is key to understanding its molecular functions. Here, for first time, we identify the full spectrum of chromatin-bound RB. Rather than exclusively binding promoters, as is often described, RB targets three fundamentally different types of loci (promoters, enhancers, and insulators), which are largely distinguishable by the mutually exclusive presence of E2F1, c-Jun, and CTCF. While E2F/DP facilitates RB association with promoters, AP-1 recruits RB to enhancers. Although phosphorylation in CDK sites is often portrayed as releasing RB from chromatin, we show that the cell cycle redistributes RB so that it enriches at promoters in G1 and at non-promoter sites in cycling cells. RB-bound promoters include the classic E2F-targets and are similar between lineages, but RB-bound enhancers associate with different categories of genes and vary between cell types. Thus, RB has a well-preserved role controlling E2F in G1, and it targets cell-type-specific enhancers and CTCF sites when cells enter S-phase.Entities:
Keywords: AP-1; CTCF; E2F; PanChIP; RB phosphorylation; RB-bound enhancers; RB-bound promoters; cell-cycle regulation; regulation of RB activity; retinoblastoma protein
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Year: 2022 PMID: 35981542 PMCID: PMC9481721 DOI: 10.1016/j.molcel.2022.07.014
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 19.328