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  • 标题:Long-distance combinatorial linkage between methylation and acetylation on histone H3 N termini
  • 本地全文:下载
  • 作者:Sean D. Taverna ; Beatrix M. Ueberheide ; Yifan Liu
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2007
  • 卷号:104
  • 期号:7
  • 页码:2086-2091
  • DOI:10.1073/pnas.0610993104
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Individual posttranslational modifications (PTMs) on histones have well established roles in certain biological processes, notably transcriptional programming. Recent genomewide studies describe patterns of covalent modifications, such as H3 methylation and acetylation at promoters of specific target genes, or "bivalent domains," in stem cells, suggestive of a possible combinatorial interplay between PTMs on the same histone. However, detection of long-range PTM associations is often problematic in antibody-based or traditional mass spectrometric-based analyses. Here, histone H3 from a ciliate model was analyzed as an enriched source of transcriptionally active chromatin. Using a recently developed mass spectrometric approach, combinatorial modification states on single, long N-terminal H3 fragments (residues 1-50) were determined. The entire modification status of intact N termini was obtained and indicated correlations between K4 methylation and H3 acetylation. In addition, K4 and K27 methylation were identified concurrently on one H3 species. This methodology is applicable to other histones and larger polypeptides and will likely be a valuable tool in understanding the roles of combinatorial patterns of PTMs.
  • 关键词:bivalent domain ; electron transfer dissociation ; mass spectrometry ; posttranslational modifications ; Tetrahymena
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