| Literature DB >> 28503659 |
Qiao Yi Chen1, Max Costa1, Hong Sun1.
Abstract
MOF was first identified in Drosophila melanogaster as an important component of the dosage compensation complex. As a member of MYST family of histone acetyltransferase, MOF specifically deposits the acetyl groups to histone H4 lysine 16. Throughout evolution, MOF and its mammalian ortholog have retained highly conserved substrate specificity and similar enzymatic activities. MOF plays important roles in dosage compensation, ESC self-renewal, DNA damage and repair, cell survival, and gene expression regulation. Dysregulation of MOF has been implicated in tumor formation and progression of many types of human cancers. This review will discuss the structure and activity of mammalian hMOF as well as its function in H4K16 acetylation, DNA damage response, stem cell pluripotency, and carcinogenesis.Entities:
Keywords: H4K16; MOF; MSL; NSL; histone acetylation
Year: 2015 PMID: 28503659 PMCID: PMC5425159 DOI: 10.3934/biophy.2015.4.555
Source DB: PubMed Journal: AIMS Biophys ISSN: 2377-9098