| Literature DB >> 23478572 |
Samuel T Keating1, Assam El-Osta2.
Abstract
Posttranslational histone modifications define chromatin structure and function. In recent years, a number of studies have characterized many of the enzymatic activities and diverse regulatory components required for monomethylation of histone H3 lysine 4 (H3K4me1) and the expression of specific genes. The challenge now is to understand how this specific chemical modification is written and the Set7 methyltransferase has emerged as a key regulatory enzyme mediating methylation of lysine residues of histone and non-histone proteins. In this review, we comprehensively explore the regulatory proteins modified by Set7 and highlight mechanisms of specific co-recruitment of the enzyme to activating promoters. With a focus on signaling and transcriptional control in disease we discuss recent experimental data emphasizing specific components of diverse regulatory complexes that mediate chromatin modification and reinterpretation of Set7-mediated gene expression.Entities:
Keywords: Set7; Set9; chromatin; epigenetics; gene expression; histone modification; lysine methylation; metabolic memory; p65
Mesh:
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Year: 2013 PMID: 23478572 PMCID: PMC3674045 DOI: 10.4161/epi.24234
Source DB: PubMed Journal: Epigenetics ISSN: 1559-2294 Impact factor: 4.528