Active genes are tri-methylated at K4 of histone H3

被引:1631
作者
Santos-Rosa, H
Schneider, R
Bannister, AJ
Sherriff, J
Bernstein, BE
Emre, NCT
Schreiber, SL
Mellor, J
Kouzarides, T
机构
[1] Wellcome Trust Canc Res UK Inst, Cambridge CG2 1QR, England
[2] Dept Pathol, Cambridge CG2 1QR, England
[3] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
[4] Harvard Univ, Dept Chem & Biol Chem, Cambridge, MA 02138 USA
[5] Wilstar Inst, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature01080
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
Lysine methylation of histones in vivo occurs in three states: mono-, di- and tri-methyl(1). Histone H3 has been found to be dimethylated at lysine 4 (K4) in active euchromatic regions but not in silent heterochromatic sites(2). Here we show that the Saccharomyces cerevisiae Set1 protein can catalyse di- and tri- methylation of K4 and stimulate the activity of many genes. Using antibodies that discriminate between the di- and tri- methylated state of K4 we show that di- methylation occurs at both inactive and active euchromatic genes, whereas tri- methylation is present exclusively at active genes. It is therefore the presence of a trimethylated K4 that defines an active state of gene expression. These findings establish the concept of methyl status as a determinant for gene activity and thus extend considerably the complexity of histone modifications.
引用
收藏
页码:407 / 411
页数:6
相关论文
共 20 条
[1]   Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain [J].
Bannister, AJ ;
Zegerman, P ;
Partridge, JF ;
Miska, EA ;
Thomas, JO ;
Allshire, RC ;
Kouzarides, T .
NATURE, 2001, 410 (6824) :120-124
[2]   Methylation of histone H3 Lys 4 in coding regions of active genes [J].
Bernstein, BE ;
Humphrey, EL ;
Erlich, RL ;
Schneider, R ;
Bouman, P ;
Liu, JS ;
Kouzarides, T ;
Schreiber, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (13) :8695-8700
[3]   Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae [J].
Briggs, SD ;
Bryk, M ;
Strahl, BD ;
Cheung, WL ;
Davie, JK ;
Dent, SYR ;
Winston, F ;
Allis, CD .
GENES & DEVELOPMENT, 2001, 15 (24) :3286-3295
[4]   Evidence that SET1, a factor required for methylation of histone H3, regulates rDNA silencing in S-cerevisiae by a sir2-independent mechanism [J].
Bryk, M ;
Briggs, SD ;
Strahl, BD ;
Curcio, MJ ;
Allis, CD ;
Winston, F .
CURRENT BIOLOGY, 2002, 12 (02) :165-170
[5]   Chemical inhibition of the Pho85 cyclin-dependent kinase reveals a role in the environmental stress response [J].
Carroll, AS ;
Bishop, AC ;
DeRisi, JL ;
Shokat, KM ;
O'Shea, EK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (22) :12578-12583
[6]   Signaling to chromatin through histone modifications [J].
Cheung, P ;
Allis, CD ;
Sassone-Corsi, P .
CELL, 2000, 103 (02) :263-271
[7]   Exploring the metabolic and genetic control of gene expression on a genomic scale [J].
DeRisi, JL ;
Iyer, VR ;
Brown, PO .
SCIENCE, 1997, 278 (5338) :680-686
[8]   Functional discovery via a compendium of expression profiles [J].
Hughes, TR ;
Marton, MJ ;
Jones, AR ;
Roberts, CJ ;
Stoughton, R ;
Armour, CD ;
Bennett, HA ;
Coffey, E ;
Dai, HY ;
He, YDD ;
Kidd, MJ ;
King, AM ;
Meyer, MR ;
Slade, D ;
Lum, PY ;
Stepaniants, SB ;
Shoemaker, DD ;
Gachotte, D ;
Chakraburtty, K ;
Simon, J ;
Bard, M ;
Friend, SH .
CELL, 2000, 102 (01) :109-126
[9]   In vivo chromatin remodeling by yeast ISWI homologs Isw1p and Isw2p [J].
Kent, NA ;
Karabetsou, N ;
Politis, PK ;
Mellor, J .
GENES & DEVELOPMENT, 2001, 15 (05) :619-626
[10]   COMPASS, a histone H3 (lysine 4) methyltransferase required for telomeric silencing of gene expression [J].
Krogan, NJ ;
Dover, J ;
Khorrami, S ;
Greenblatt, JF ;
Schneider, J ;
Johnston, M ;
Shilatifard, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) :10753-10755