Drosophila Set1 is the major histone H3 lysine 4 trimethyltransferase with role in transcription

被引:145
作者
Ardehali, M. Behfar [1 ]
Mei, Amanda
Zobeck, Katie L. [1 ]
Caron, Matthieu
Lis, John T. [1 ]
Kusch, Thomas [2 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
[2] Rutgers State Univ, Dept Mol Biol & Biochem, Nelson Biol Labs, Piscataway, NJ 08854 USA
基金
美国国家卫生研究院;
关键词
Drosophila; dSet1; heat shock; H3; lysine; 4; methylation; transcription elongation; RNA-POLYMERASE-II; CXXC FINGER PROTEIN-1; LITTLE-IMAGINAL-DISCS; METHYLTRANSFERASE COMPLEX; SACCHAROMYCES-CEREVISIAE; CHROMATIN-STRUCTURE; TRITHORAX; METHYLATION; GENE; BINDING;
D O I
10.1038/emboj.2011.194
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Histone H3 lysine 4 trimethylation (H3K4me3) is a major hallmark of promoter-proximal histones at transcribed genes. Here, we report that a previously uncharacterized Drosophila H3K4 methyltransferase, dSet1, and not the other putative histone H3K4 methyltransferases (Trithorax; Trithorax-related protein), is predominantly responsible for histone H3K4 trimethylation. Functional and proteomics studies reveal that dSet1 is a component of a conserved H3K4 trimethyltransferase complex and polytene staining and live cell imaging assays show widespread association of dSet1 with transcriptionally active genes. dSet1 is present at the promoter region of all tested genes, including activated Hsp70 and Hsp26 heat shock genes and is required for optimal mRNA accumulation from the tested genes. In the case of Hsp70, the mRNA production defect in dSet1 RNAi-treated cells is accompanied by retention of Pol II at promoters. Our data suggest that dSet1-dependent H3K4me3 is responsible for the generation of a chromatin structure at active promoters that ensures optimal Pol II release into productive elongation. The EMBO Journal ( 2011) 30, 2817-2828. doi:10.1038/emboj.2011.194; Published online 21 June 2011
引用
收藏
页码:2817 / 2828
页数:12
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