Set2 Is a Nucleosomal Histone H3-Selective Methyltransferase That Mediates Transcriptional Repression
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- 1 March 2002
- journal article
- research article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 22 (5) , 1298-1306
- https://doi.org/10.1128/mcb.22.5.1298-1306.2002
Abstract
Recent studies of histone methylation have yielded fundamental new insights pertaining to the role of this modification in gene activation as well as in gene silencing. While a number of methylation sites are known to occur on histones, only limited information exists regarding the relevant enzymes that mediate these methylation events. We thus sought to identify native histone methyltransferase (HMT) activities from Saccharomyces cerevisiae. Here, we describe the biochemical purification and characterization of Set2, a novel HMT that is site-specific for lysine 36 (Lys36) of the H3 tail. Using an antiserum directed against Lys36 methylation in H3, we show that Set2, via its SET domain, is responsible for methylation at this site in vivo. Tethering of Set2 to a heterologous promoter reveals that Set2 represses transcription, and part of this repression is mediated through the HMT activity of the SET domain. These results suggest that Set2 and methylation at H3 Lys36 play a role in the repression of gene transcription.Keywords
This publication has 43 references indexed in Scilit:
- Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiaeGenes & Development, 2001
- Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tailsGenes & Development, 2001
- Translating the Histone CodeScience, 2001
- The bromodomain: a chromatin browser?Frontiers in Bioscience-Landmark, 2001
- Review: Chromatin Structural Features and Targets That Regulate TranscriptionJournal of Structural Biology, 2000
- The language of covalent histone modificationsNature, 2000
- SMART: a web-based tool for the study of genetically mobile domainsNucleic Acids Research, 2000
- The “Dark Side” of Chromatin RemodelingCell, 1999
- ALTERATION OF NUCLEOSOME STRUCTURE AS A MECHANISM OF TRANSCRIPTIONAL REGULATIONAnnual Review of Biochemistry, 1998
- Improvement and simplification of low‐background silver staining of proteins by using sodium dithioniteElectrophoresis, 1988