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
  • [1] Regulated recruitment of HP1 to a euchromatic gene induces mitotically heritable, epigenetic gene silencing: a mammalian cell culture model of gene variegation
    Ayyanathan, K
    Lechner, MS
    Bell, P
    Maul, GG
    Schultz, DC
    Yamada, Y
    Tanaka, K
    Torigoe, K
    Rauscher, FJ
    [J]. GENES & DEVELOPMENT, 2003, 17 (15) : 1855 - 1869
  • [2] Rex-1, a gene encoding a transcription factor expressed in rbe early embryo, is regulated via Oct-3/4 and Oct-6 binding to an Octamer site and a novel protein, Rox-1, binding to an adjacent site
    Ben-Shushan, E
    Thompson, JR
    Gudas, LJ
    Bergman, Y
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) : 1866 - 1878
  • [3] BENSHUSHAN E, 1995, MOL CELL BIOL, V15, P1034
  • [4] Oct4 distribution and level in mouse clones:: consequences for pluripotency
    Boiani, M
    Eckardt, S
    Schöler, HR
    McLaughlin, KJ
    [J]. GENES & DEVELOPMENT, 2002, 16 (10) : 1209 - 1219
  • [5] Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei
    Bortvin, A
    Eggan, K
    Skaletsky, H
    Akutsu, H
    Berry, DL
    Yanagimachi, R
    Page, DC
    Jaenisch, R
    [J]. DEVELOPMENT, 2003, 130 (08): : 1673 - 1680
  • [6] SP1 ELEMENTS PROTECT A CPG ISLAND FROM DE-NOVO METHYLATION
    BRANDEIS, M
    FRANK, D
    KESHET, I
    SIEGFRIED, Z
    MENDELSOHN, M
    NEMES, A
    TEMPER, V
    RAZIN, A
    CEDAR, H
    [J]. NATURE, 1994, 371 (6496) : 435 - 438
  • [7] Oct-4: more than just a POUerful marker of the mammalian germline?
    Brehm, A
    Ovitt, CE
    Scholer, HR
    [J]. APMIS, 1998, 106 (01) : 114 - 124
  • [8] Heterochromatin: stable and unstable invasions at home and abroad
    Fahrner, JA
    Baylin, SB
    [J]. GENES & DEVELOPMENT, 2003, 17 (15) : 1805 - 1812
  • [9] Controlling DNA methylation: many roads to one modification
    Freitag, M
    Selker, EU
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 2005, 15 (02) : 191 - 199
  • [10] Mouse germline restriction of Oct4 expression by germ cell nuclear factor
    Fuhrmann, G
    Chung, ACK
    Jackson, KJ
    Hummelke, G
    Baniahmad, A
    Sutter, J
    Sylvester, I
    Schöler, HR
    Cooney, AJ
    [J]. DEVELOPMENTAL CELL, 2001, 1 (03) : 377 - 387