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RPA Interacts with HIRA and Regulates H3.3 Deposition at Gene Regulatory Elements in Mammalian Cells
- Source :
- Molecular Cell. 65:272-284
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- The histone chaperone HIRA is involved in depositing histone variant H3.3 into distinct genic regions, including promoters, enhancers, and gene bodies. However, how HIRA deposits H3.3 to these regions remains elusive. Through a short hairpin RNA (shRNA) screening, we identified single-stranded DNA binding protein replication protein A (RPA) as a regulator of the deposition of newly synthesized H3.3 into chromatin. We show that RPA physically interacts with HIRA to form RPA-HIRA-H3.3 complexes, and it co-localizes with HIRA and H3.3 at gene promoters and enhancers. Depletion of RPA1, the largest subunit of the RPA complex, dramatically reduces both HIRA association with chromatin and the deposition of newly synthesized H3.3 at promoters and enhancers and leads to altered transcription at gene promoters. These results support a model whereby RPA, best known for its role in DNA replication and repair, recruits HIRA to promoters and enhancers and regulates deposition of newly synthesized H3.3 to these regulatory elements for gene regulation.
- Subjects :
- 0301 basic medicine
Transcription, Genetic
Cell Cycle Proteins
Transfection
complex mixtures
Article
Histones
03 medical and health sciences
Transcription (biology)
Replication Protein A
Humans
Histone Chaperones
Protein Interaction Domains and Motifs
Promoter Regions, Genetic
Enhancer
Molecular Biology
Replication protein A
Gene
Regulation of gene expression
Binding Sites
biology
G1 Phase
Promoter
DNA
Cell Biology
Molecular biology
Chromatin
DNA-Binding Proteins
Enhancer Elements, Genetic
HEK293 Cells
030104 developmental biology
Histone
biology.protein
RNA Interference
HeLa Cells
Protein Binding
Transcription Factors
Subjects
Details
- ISSN :
- 10972765
- Volume :
- 65
- Database :
- OpenAIRE
- Journal :
- Molecular Cell
- Accession number :
- edsair.doi.dedup.....64e49e483f792883248603c0982b1235