Recognition of trimethylated histone H3 lysine 4 facilitates the recruitment of transcription postinitiation factors and pre-mRNA splicing Journal Article


Authors: Sims, R. J. 3rd; Millhouse, S.; Chen, C. F.; Lewis, B. A.; Erdjument-Bromage, H.; Tempst, P.; Manley, J. L.; Reinberg, D.
Article Title: Recognition of trimethylated histone H3 lysine 4 facilitates the recruitment of transcription postinitiation factors and pre-mRNA splicing
Abstract: Trimethylation of histone H3 on lysine 4 (H3K4me3) localizes near the 5′ region of genes and is tightly associated with active loci. Several proteins, such as CHD1, BPTF, JMJD2A, and the ING tumor suppressor family, directly recognize this lysine methyl mark. However, how H3K4me3 recognition participates in active transcription remains poorly characterized. Here we identify specific CHD1-interacting proteins via H3K4me3 affinity purification, including numerous factors mediating postinitiation events. Conventional biochemical purification revealed a stable complex between CHD1 and components of the spliceosome. Depletion of CHD1 in extracts dramatically reduced splicing efficiency in vitro, indicating a functional link between CHD1 and the spliceosome. Knockdown of CHD1 and H3K4me3 levels by siRNA reduced association of U2 snRNP components with chromatin and, more importantly, altered the efficiency of pre-mRNA splicing on active genes in vivo. These findings suggest that methylated H3K4 serves to facilitate the competency of pre-mRNA maturation through the bridging of spliceosomal components to H3K4me3 via CHD1. © 2007 Elsevier Inc. All rights reserved.
Keywords: unclassified drug; methylation; dna-binding proteins; protein analysis; small interfering rna; protein binding; gene locus; protein interaction; transcription, genetic; hela cells; transcription factors; rna; dna; protein purification; chromatin; histone h3; peptides; models, genetic; spliceosome; histones; dna helicases; lysine; rna splicing; rna precursors; spliceosomes; protein bptf; protein chd1; protein jmjd2a; ribonucleoprotein, u2 small nuclear
Journal Title: Molecular Cell
Volume: 28
Issue: 4
ISSN: 1097-2765
Publisher: Cell Press  
Date Published: 2007-11-30
Start Page: 665
End Page: 676
Language: English
DOI: 10.1016/j.molcel.2007.11.010
PUBMED: 18042460
PROVIDER: scopus
PMCID: PMC2276655
DOI/URL:
Notes: --- - "Cited By (since 1996): 130" - "Export Date: 17 November 2011" - "CODEN: MOCEF" - "Source: Scopus"
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  1. Paul J Tempst
    324 Tempst