Genome-wide maps of chromatin state for H3.3 tagged cells
Source: NCBI BioProject (ID PRJNA192851)
Source: NCBI BioProject (ID PRJNA192851)
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Project name: Homo sapiens
Description: The HIRA chaperone complex, comprised of HIRA, UBN1 and CABIN1, collaborates with histone-binding protein ASF1a to incorporate histone variant H3.3 into chromatin in a DNA replication-independent manner. To better understand its function and mechanism, we integrated HIRA, UBN1, ASF1a and histone H3.3 ChIP-seq and gene expression analyses. Most HIRA-binding sites co-localize with UBN1, ASF1a and H3.3 at active promoters and active and weak/poised enhancers. At promoters, binding of HIRA/UBN1/ASF1a correlates with the level of gene expression. HIRA is required for deposition of histone H3.3 at its binding sites. There are marked differences in nucleosome and co-regulator composition at different classes of HIRA-bound regulatory site. Underscoring this, we report novel physical interactions between the HIRA complex and transcription factors, a chromatin insulator and an ATP-dependent chromatin-remodelling complex. Our results map the distribution of the HIRA chaperone across the chromatin landscape and point to different interacting partners at functionally distinct regulatory sites.Overall design: Examination of H3.3 histone modification in HeLA cells with accompanying FAIRE data
Data type: Other
Sample scope: Multiisolate
Relevance: Medical
Organization: University of Glasgow, Beatson Institute for Cancer Research
Literatures
- PMID: 23602572
Last updated: 2013-03-11