Pluripotency governed by Sox2 via regulation of Oct3/4 expression in mouse embryonic stem cells

被引:889
作者
Masui, Shinji
Nakatake, Yuhki
Toyooka, Yayoi
Shimosato, Daisuke
Yagi, Rika
Takahashi, Kazue
Okochi, Hitoshi
Okuda, Akihiko
Matoba, Ryo
Sharov, Alexei A.
Ko, Minoru S. H.
Niwa, Hitoshi
机构
[1] RIKEN, Ctr Dev Biol, Lab Pluripotent Cell Studies, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] CREST, Japan Sci & Technol Agcy, Kawaguchi, Saitama 3320012, Japan
[3] Int Med Ctr Japan, Div Mol Biol & Cell Engn, Dept Regenerat Med, Res Inst,Shinjuku Ku, Tokyo 1628655, Japan
[4] Kobe Univ, Lab Dev & Regenerat Med, Grad Sch Med, Chuo Ku, Kobe, Hyogo 6500017, Japan
[5] Saitama Med Univ, Div Dev Biol, Res Ctr Genom Med, Hidaka, Saitama 3501241, Japan
[6] NIA, NIH, Dev Genom & Aging Sect, Genet Lab, Baltimore, MD 21224 USA
关键词
D O I
10.1038/ncb1589
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The pluripotency of embryonic stem (ES) cells is thought to be maintained by a few key transcription factors, including Oct3/4 and Sox2. The function of Oct3/4 in ES cells has been extensively characterized, but that of Sox2 has yet to be determined. Sox2 can act synergistically with Oct3/4 in vitro to activate Oct-Sox enhancers, which regulate the expression of pluripotent stem cell-specific genes, including Nanog, Oct3/4 and Sox2 itself. These findings suggest that Sox2 is required by ES cells for its Oct-Sox enhancer activity. Using inducible Sox2-null mouse ES cells, we show that Sox2 is dispensable for the activation of these Oct-Sox enhancers. In contrast, we demonstrate that Sox2 is necessary for regulating multiple transcription factors that affect Oct3/4 expression and that the forced expression of Oct3/4 rescues the pluripotency of Sox2-null ES cells. These results indicate that the essential function of Sox2 is to stabilize ES cells in a pluripotent state by maintaining the requisite level of Oct3/4 expression.
引用
收藏
页码:625 / U26
页数:15
相关论文
共 50 条
  • [11] Orphan nuclear receptor GCNF is required for the repression of pluripotency genes during retinoic acid-induced embryonic stem cell differentiation
    Gu, PL
    LeMenuet, D
    Chung, ACK
    Mancini, M
    Wheeler, DA
    Cooney, AJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (19) : 8507 - 8519
  • [12] Orphan nuclear receptor LRH-1 is required to maintain Oct4 expression at the epiblast stage of embryonic development
    Gu, PL
    Goodwin, B
    Chung, ACK
    Xu, XP
    Wheeler, DA
    Price, RR
    Galardi, C
    Peng, L
    Latour, AM
    Koller, BH
    Gossen, J
    Kliewer, SA
    Cooney, AJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (09) : 3492 - 3505
  • [13] HPRT-DEFICIENT (LESCH-NYHAN) MOUSE EMBRYOS DERIVED FROM GERMLINE COLONIZATION BY CULTURED-CELLS
    HOOPER, M
    HARDY, K
    HANDYSIDE, A
    HUNTER, S
    MONK, M
    [J]. NATURE, 1987, 326 (6110) : 292 - 295
  • [14] Dissecting self-renewal in stem cells with RNA interference
    Ivanova, Natalia
    Dobrin, Radu
    Lu, Rong
    Kotenko, Iulia
    Levorse, John
    DeCoste, Christina
    Schafer, Xenia
    Lun, Yi
    Lemischka, Ihor R.
    [J]. NATURE, 2006, 442 (7102) : 533 - 538
  • [15] Kamachi Y, 1998, DEVELOPMENT, V125, P2521
  • [16] Induction of midbrain dopaminergic neurons from ES cells by stromal cell-derived inducing activity
    Kawasaki, H
    Mizuseki, K
    Nishikawa, S
    Kaneko, S
    Kuwana, Y
    Nakanishi, S
    Nishikawa, S
    Sasai, Y
    [J]. NEURON, 2000, 28 (01) : 31 - 40
  • [17] Octamer and Sox elements are required for transcriptional cis regulation of Nanog gene expression
    Kuroda, T
    Tada, M
    Kubota, H
    Kimura, H
    Hatano, S
    Suemori, H
    Nakatsuji, N
    Tada, T
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (06) : 2475 - 2485
  • [18] Requirement for Wnt3 in vertebrate axis formation
    Liu, PT
    Wakamiya, M
    Shea, MJ
    Albrecht, U
    Behringer, RR
    Bradley, A
    [J]. NATURE GENETICS, 1999, 22 (04) : 361 - 365
  • [19] The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells
    Loh, YH
    Wu, Q
    Chew, JL
    Vega, VB
    Zhang, WW
    Chen, X
    Bourque, G
    George, J
    Leong, B
    Liu, J
    Wong, KY
    Sung, KW
    Lee, CWH
    Zhao, XD
    Chiu, KP
    Lipovich, L
    Kuznetsov, VA
    Robson, P
    Stanton, LW
    Wei, CL
    Ruan, YJ
    Lim, B
    Ng, HH
    [J]. NATURE GENETICS, 2006, 38 (04) : 431 - 440
  • [20] DOMINANT POSITIVE AND NEGATIVE SELECTION USING A HYGROMYCIN PHOSPHOTRANSFERASE-THYMIDINE KINASE FUSION GENE
    LUPTON, SD
    BRUNTON, LL
    KALBERG, VA
    OVERELL, RW
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (06) : 3374 - 3378