G9a-mediated irreversible epigenetic inactivation of Oct-3/4 during early embryogenesis

被引:490
作者
Feldman, N
Gerson, A
Fang, J
Li, E
Zhang, Y
Shinkai, Y
Cedar, H
Bergman, Y [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Med, Dept Expt Med, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Sch Med, Dept Cellular Biochem, IL-91120 Jerusalem, Israel
[3] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[4] Massachusetts Gen Hosp, Cutaneous Biol Res Ctr, Charlestown, MA 02129 USA
[5] Kyoto Univ, Inst Virus Res, Expt Res Ctr Infect Dis, Sakyo Ku, Kyoto 6068507, Japan
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ncb1353
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Oct-3/4 is a POU domain homeobox gene that is expressed during gametogenesis and in early embryonic cells(1,2), where it has been shown to be important for maintaining pluripotency(3). Following implantation, this gene undergoes a novel multi-step programme of inactivation. Transcriptional repression is followed by a pronounced increase in histone H3 methylation on Lys 9 that is mediated by the SET-containing protein, G9a. This step sets the stage for local heterochromatinization via the binding of HP1 and is required for subsequent de novo methylation at the promoter by the enzymes Dnmt3a/3b. Genetic studies show that these epigenetic changes actually have an important role in the inhibition of Oct-3/4 reexpression, thereby preventing reprogramming.
引用
收藏
页码:188 / U55
页数:10
相关论文
共 33 条
  • [21] DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
    Okano, M
    Bell, DW
    Haber, DA
    Li, E
    [J]. CELL, 1999, 99 (03) : 247 - 257
  • [22] Targeted inhibition of V(D)J recombination by a histone methyltransferase
    Osipovich, O
    Milley, R
    Meade, A
    Tachibana, M
    Shinkai, Y
    Krangel, MS
    Oltz, EM
    [J]. NATURE IMMUNOLOGY, 2004, 5 (03) : 309 - 316
  • [23] Pesce M, 2000, MOL REPROD DEV, V55, P452, DOI 10.1002/(SICI)1098-2795(200004)55:4&lt
  • [24] 452::AID-MRD14&gt
  • [25] 3.0.CO
  • [26] 2-S
  • [27] RETINOIC ACID REPRESSES OCT-3/4 GENE-EXPRESSION THROUGH SEVERAL RETINOIC ACID-RESPONSIVE ELEMENTS LOCATED IN THE PROMOTER-ENHANCER REGION
    PIKARSKY, E
    SHARIR, H
    BENSHUSHAN, E
    BERGMAN, Y
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (02) : 1026 - 1038
  • [28] Active genes are tri-methylated at K4 of histone H3
    Santos-Rosa, H
    Schneider, R
    Bannister, AJ
    Sherriff, J
    Bernstein, BE
    Emre, NCT
    Schreiber, SL
    Mellor, J
    Kouzarides, T
    [J]. NATURE, 2002, 419 (6905) : 407 - 411
  • [29] DNA demethylation is necessary for the epigenetic reprogramming of somatic cell nuclei
    Simonsson, S
    Gurdon, J
    [J]. NATURE CELL BIOLOGY, 2004, 6 (10) : 984 - 990
  • [30] Relationship between histone H3 lysine 9 methylation, transcription repression, and heterochromatin protein 1 recruitment
    Stewart, MD
    Li, JW
    Wong, JM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (07) : 2525 - 2538