Methylation of histone H3 Lys 4 in coding regions of active genes

被引:578
作者
Bernstein, BE
Humphrey, EL
Erlich, RL
Schneider, R
Bouman, P
Liu, JS
Kouzarides, T
Schreiber, SL [1 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Howard Hughes Med Inst, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[3] Harvard Univ, Howard Hughes Med Inst, Dept Stat, Cambridge, MA 02138 USA
[4] Harvard Univ, Ctr Genom Res, Cambridge, MA 02138 USA
[5] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[6] Wellcome Canc Res Campaign Inst, Cambridge CB2 1QR, England
[7] Dept Pathol, Cambridge CB2 1QR, England
关键词
D O I
10.1073/pnas.082249499
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Posttranslational modifications of histone tails regulate chromatin structure and transcription. Here we present global analyses of histone acetylation and histone H3 Lys 4 methylation patterns in yeast. We observe a significant correlation between acetylation of histories H3 and H4 in promoter regions and transcriptional activity. In contrast, we find that dimethylation of histone H3 Lys 4 in coding regions correlates with transcriptional activity. The histone methyltransferase Set1 is required to maintain expression of these active, promoter-acetylated, and coding region-methylated genes. Global comparisons reveal that genomic regions deacetylated by the yeast enzymes Rpd3 and Hda1 overlap extensively with Lys 4 hypo- but not hypermethylated regions. In the context of recent studies showing that Lys 4 methylation precludes histone deacetylase recruitment, we conclude that Set1 facilitates transcription, in part, by protecting active coding regions from deacetylation.
引用
收藏
页码:8695 / 8700
页数:6
相关论文
共 44 条
  • [1] Genomewide studies of histone deacetylase function in yeast
    Bernstein, BE
    Tong, JK
    Schreiber, SL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) : 13708 - 13713
  • [2] Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes
    Boggs, BA
    Cheung, P
    Heard, E
    Spector, DL
    Chinault, AC
    Allis, CD
    [J]. NATURE GENETICS, 2002, 30 (01) : 73 - 76
  • [3] TRANSCRIPTIONAL SILENCING IN YEAST IS ASSOCIATED WITH REDUCED NUCLEOSOME ACETYLATION
    BRAUNSTEIN, M
    ROSE, AB
    HOLMES, SG
    ALLIS, CD
    BROACH, JR
    [J]. GENES & DEVELOPMENT, 1993, 7 (04) : 592 - 604
  • [4] Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae
    Briggs, SD
    Bryk, M
    Strahl, BD
    Cheung, WL
    Davie, JK
    Dent, SYR
    Winston, F
    Allis, CD
    [J]. GENES & DEVELOPMENT, 2001, 15 (24) : 3286 - 3295
  • [5] Chemical inhibition of the Pho85 cyclin-dependent kinase reveals a role in the environmental stress response
    Carroll, AS
    Bishop, AC
    DeRisi, JL
    Shokat, KM
    O'Shea, EK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (22) : 12578 - 12583
  • [6] The genome-wide localization of Rsc9, a component of the RSC chromatin-remodeling complex, changes in response to stress
    Damelin, M
    Simon, I
    Moy, TI
    Wilson, B
    Komili, S
    Tempst, P
    Roth, FP
    Young, RA
    Cairns, BR
    Silver, PA
    [J]. MOLECULAR CELL, 2002, 9 (03) : 563 - 573
  • [7] Exploring the metabolic and genetic control of gene expression on a genomic scale
    DeRisi, JL
    Iyer, VR
    Brown, PO
    [J]. SCIENCE, 1997, 278 (5338) : 680 - 686
  • [8] Localization of Sir2p: The nucleolus as a compartment for silent information regulators
    Gotta, M
    StrahlBolsinger, S
    Renauld, H
    Laroche, T
    Kennedy, BK
    Grunstein, M
    Gasser, SM
    [J]. EMBO JOURNAL, 1997, 16 (11) : 3243 - 3255
  • [9] Hecht A, 1999, METHOD ENZYMOL, V304, P399
  • [10] Dissecting the regulatory circuitry of a eukaryotic genome
    Holstege, FCP
    Jennings, EG
    Wyrick, JJ
    Lee, TI
    Hengartner, CJ
    Green, MR
    Golub, TR
    Lander, ES
    Young, RA
    [J]. CELL, 1998, 95 (05) : 717 - 728