Proteomics

Dataset Information

0

Affinity Purification experiments for 24 human Bromodomain proteins involved in DNA repair and genome integrity (part 2 of 2)


ABSTRACT: Bromodomain proteins (BRD) are key chromatin regulators of genome function and stability, as well as therapeutic targets in cancer. In our associated publication (doi:10.1101/gad.331231.119) we systematically delineate the contribution of human BRD proteins for genome stability and DNA double-strand break (DSB) repair using cell-based assays and proteomic interaction network analysis. These AP-MS experiments were performed in order to construct a protein interaction network for the 24 BRDs we identified as promoters of DNA repair and/or genome integrity: BAZ1B, BRD1, BRD2, BRD3, BRD4, BRD8, BRD9, BRPF3, BRWD3, CECR2, EP300, GCN5/KAT2A, PCAF/KAT2B, PHIP, SMARCA2, SP100, SP110, SP140, TAF1, TRIM24, TRIM28, TRIM33, TRIM66, ZMYND8. In combination with cell based assays, we identified a BRD-reader function of PCAF that bound TIP60-mediated histone acetylations at DSBs to recruit a DUB complex to deubiquitylate histone H2BK120, to allow direct acetylation by PCAF and repair of DSBs by homologous recombination. We also discovered the bromo-and-extra-terminal (BET) BRD proteins, BRD2 and BRD4, as negative regulators of transcription-associated RNA-DNA hybrid (R-Loop) as inhibition of BRD2 or BRD4 increased R-loop formation, which generated DSBs. These breaks were reliant on Topoisomerase II and BRD2 directly bound and activated Topoisomerase I, a known restrainer of R-loops. Thus, comprehensive interactome and functional profiling of BRD proteins revealed new homologous recombination and genome stability pathways, providing a strategy to understand genome maintenance by BRD proteins and the effects of their pharmacological inhibition. This accession provides AP-MS experiment files for the following subset of 6 BRDs: BRD9, EP300, GCN5/KAT2A, PCAF/KAT2B, SP140, TRIM28, as well as their associated controls (Input, Mock, and SBP-tagged NLS).

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Hek-293t Cell

SUBMITTER: Anna Battenhouse  

LAB HEAD: Kyle M. Miller

PROVIDER: PXD016673 | Pride | 2019-12-12

REPOSITORIES: Pride

altmetric image

Publications

Systematic bromodomain protein screens identify homologous recombination and R-loop suppression pathways involved in genome integrity.

Kim Jae Jin JJ   Lee Seo Yun SY   Gong Fade F   Battenhouse Anna M AM   Boutz Daniel R DR   Bashyal Aarti A   Refvik Samantha T ST   Chiang Cheng-Ming CM   Xhemalce Blerta B   Paull Tanya T TT   Brodbelt Jennifer S JS   Marcotte Edward M EM   Miller Kyle M KM  

Genes & development 20191121 23-24


Bromodomain proteins (BRD) are key chromatin regulators of genome function and stability as well as therapeutic targets in cancer. Here, we systematically delineate the contribution of human BRD proteins for genome stability and DNA double-strand break (DSB) repair using several cell-based assays and proteomic interaction network analysis. Applying these approaches, we identify 24 of the 42 BRD proteins as promoters of DNA repair and/or genome integrity. We identified a BRD-reader function of PC  ...[more]

Similar Datasets

2019-12-12 | PXD016700 | Pride
2019-11-12 | PXD014441 | Pride
2012-07-30 | E-GEOD-39580 | biostudies-arrayexpress
2012-07-31 | E-GEOD-39579 | biostudies-arrayexpress
2021-03-01 | E-MTAB-9688 | biostudies-arrayexpress
2021-04-01 | PXD019923 | Pride
2017-03-01 | GSE63778 | GEO
2017-03-13 | GSE90788 | GEO
2022-06-09 | PXD027727 | Pride
2021-03-16 | GSE156423 | GEO