The Polycomb Repressive Complex 1 Protein BMI1 Is Required for Constitutive Heterochromatin Formation and Silencing in Mammalian Somatic Cells *
Journal of Biological Chemistry, ISSN: 0021-9258, Vol: 291, Issue: 1, Page: 182-197
2016
- 28Citations
- 90Captures
- 1Mentions
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Metrics Details
- Citations28
- Citation Indexes28
- CrossRef28
- 28
- Captures90
- Readers90
- 90
- Mentions1
- Blog Mentions1
- Blog1
Article Description
The polycomb repressive complex 1 (PRC1), containing the core BMI1 and RING1A/B proteins, mono-ubiquitinylates histone H2A (H2A ub ) and is associated with silenced developmental genes at facultative heterochromatin. It is, however, assumed that the PRC1 is excluded from constitutive heterochromatin in somatic cells based on work performed on mouse embryonic stem cells and oocytes. We show here that BMI1 is required for constitutive heterochromatin formation and silencing in human and mouse somatic cells. BMI1 was highly enriched at intergenic and pericentric heterochromatin, co-immunoprecipitated with the architectural heterochromatin proteins HP1, DEK1, and ATRx, and was required for their localization. In contrast, BRCA1 localization was BMI1-independent and partially redundant with that of BMI1 for H2A ub deposition, constitutive heterochromatin formation, and silencing. These observations suggest a dynamic and developmentally regulated model of PRC1 occupancy at constitutive heterochromatin, and where BMI1 function in somatic cells is to stabilize the repetitive genome. BMI1 silences the expression of genes located at the facultative heterochromatin. BMI1 is abundant at repetitive genomic regions, including the pericentromeric heterochromatin (PCH), where it is required for compaction and silencing. BMI1 is essential for PCH formation. BMI1 function at PCH is important to understand how BMI1 regulates genomic stability.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0021925820362499; http://dx.doi.org/10.1074/jbc.m115.662403; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84952901440&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/26468281; https://linkinghub.elsevier.com/retrieve/pii/S0021925820362499; http://www.jbc.org/lookup/doi/10.1074/jbc.M115.662403; https://syndication.highwire.org/content/doi/10.1074/jbc.M115.662403; https://dx.doi.org/10.1074/jbc.m115.662403
Elsevier BV
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