RETRACTED: Histone methylation by the Drosophila epigenetic transcriptional regulator Ash1 (Retracted article. See vol. 521, pg. 110, 2015)

被引:233
作者
Beisel, C
Imhof, A
Greene, J
Kremmer, E
Sauer, F
机构
[1] Heidelberg Univ, Zentrum Mol Biol, D-69120 Heidelberg, Germany
[2] Univ Munich, Adolf Butenandt Inst, D-80336 Munich, Germany
[3] Univ Calif Riverside, Dept Biochem, Riverside, CA 92521 USA
[4] GSF Munich, Forschungszentrum, Inst Mol Immunol, D-81377 Munich, Germany
关键词
D O I
10.1038/nature01126
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
The establishment and maintenance of mitotic and meiotic stable (epigenetic) transcription patterns is fundamental for cell determination and function(1). Epigenetic regulation of transcription is mediated by epigenetic activators and repressors, and may require the establishment, 'spreading' and maintenance of epigenetic signals(2). Although these signals remain unclear, it has been proposed that chromatin structure and consequently post-translational modification of histones may have an important role in epigenetic gene expression(3,4). Here we show that the epigenetic activator Ash1 (ref. 5) is a multi-catalytic histone methyl-transferase (HMTase) that methylates lysine residues 4 and 9 in H3 and 20 in H4. Transcriptional activation by Ash1 coincides with methylation of these three lysine residues at the promoter of Ash1 target genes. The methylation pattern placed by Ash1 may serve as a binding surface for a chromatin remodelling complex containing the epigenetic activator Brahma (Brm)(6), an ATPase, and inhibits the interaction of epigenetic repressors with chromatin. Chromatin immunoprecipitation indicates that epigenetic activation of Ultrabithorax transcription in Drosophila coincides with trivalent methylation by Ash1 and recruitment of Brm. Thus, histone methylation by Ash1 may provide a specific signal for the establishment of epigenetic, active transcription patterns.
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页码:857 / 862
页数:7
相关论文
共 30 条
  • [1] Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain
    Bannister, AJ
    Zegerman, P
    Partridge, JF
    Miska, EA
    Thomas, JO
    Allshire, RC
    Kouzarides, T
    [J]. NATURE, 2001, 410 (6824) : 120 - 124
  • [2] 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
  • [3] Epigenetic inheritance of active chromatin after removal of the main transactivator
    Cavalli, G
    Paro, R
    [J]. SCIENCE, 1999, 286 (5441) : 955 - 958
  • [4] Elfring LK, 1998, GENETICS, V148, P251
  • [5] Kuo MH, 1998, BIOESSAYS, V20, P615, DOI 10.1002/(SICI)1521-1878(199808)20:8<615::AID-BIES4>3.0.CO
  • [6] 2-H
  • [7] In vivo cross-linking and immunoprecipitation for studying dynamic protein:: DNA associations in chromatin environment
    Kuo, MH
    Allis, CD
    [J]. METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1999, 19 (03): : 425 - 433
  • [8] Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins
    Lachner, M
    O'Carroll, N
    Rea, S
    Mechtler, K
    Jenuwein, T
    [J]. NATURE, 2001, 410 (6824) : 116 - 120
  • [9] TRANSREGULATION OF THORACIC HOMEOTIC SELECTOR GENES OF THE ANTENNAPEDIA AND BITHORAX COMPLEXES BY THE TRITHORAX GROUP GENES - ABSENT, SMALL, AND HOMEOTIC DISC-1 AND DISC-2
    LAJEUNESSE, D
    SHEARN, A
    [J]. MECHANISMS OF DEVELOPMENT, 1995, 53 (01) : 123 - 139
  • [10] TRANSCRIPTION ACTIVATION BY THE ADENOVIRUS E1A PROTEIN
    LILLIE, JW
    GREEN, MR
    [J]. NATURE, 1989, 338 (6210) : 39 - 44