E2F repression by C/EBPα is required for adipogenesis and granulopoiesis in vivo

被引:278
作者
Porse, BT
Pedersen, TÅ
Xu, XF
Lindberg, B
Wewer, UM
Friis-Hansen, L
Nerlov, C [1 ]
机构
[1] Univ Copenhagen Hosp, Lab Gene Therapy Res, DK-2100 Copenhagen O, Denmark
[2] Univ Copenhagen Hosp, Inst Pathol, DK-2100 Copenhagen, Denmark
[3] Univ Copenhagen Hosp, Dept Clin Biochem, DK-2100 Copenhagen O, Denmark
关键词
D O I
10.1016/S0092-8674(01)00516-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The C/EBP alpha transcription factor is required for differentiation of adipocytes and neutrophil granulocytes, and controls cellular proliferation in vivo. To address the molecular mechanisms of C/EBP alpha action, we have identified C/EBP alpha mutants defective in repression of E2F-dependent transcription and found them to be impaired in their ability to suppress cellular proliferation, and to induce adipocyte differentiation in vitro. Using targeted mutagenesis of the mouse germline, we show that E2F repression-deficient C/EBP alpha alleles failed to support adipocyte and granulocyte differentiation in vivo. These results indicate that E2F repression by C/EBP alpha is critical for its ability to induce terminal differentiation, and thus provide genetic evidence that direct cell cycle control by a mammalian lineageinstructive transcription factor couples cellular growth arrest and differentiation.
引用
收藏
页码:247 / 258
页数:12
相关论文
共 40 条
  • [31] CCAAT/enhancer binding protein alpha regulates p21 protein and hepatocyte proliferation in newborn mice
    Timchenko, NA
    Harris, TE
    Wilde, M
    Bilyeu, TA
    BurgessBeusse, BL
    Finegold, MJ
    Darlington, GJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (12) : 7353 - 7361
  • [32] Timchenko NA, 1999, MOL CELL BIOL, V19, P2936
  • [33] Mutation of E2f-1 suppresses apoptosis and inappropriate S phase entry and extends surival of Rb-deficient mouse embryos
    Tsai, KY
    Hu, YW
    Macleod, KF
    Crowley, D
    Yamasaki, L
    Jacks, T
    [J]. MOLECULAR CELL, 1998, 2 (03) : 293 - 304
  • [34] CCAAT-ENHANCER BINDING-PROTEIN - A COMPONENT OF A DIFFERENTIATION SWITCH
    UMEK, RM
    FRIEDMAN, AD
    MCKNIGHT, SL
    [J]. SCIENCE, 1991, 251 (4991) : 288 - 292
  • [35] Vigo E, 1999, MOL CELL BIOL, V19, P6379
  • [36] WANG J, 1995, CELL GROWTH DIFFER, V6, P1299
  • [37] IMPAIRED ENERGY HOMEOSTASIS IN C/EBP-ALPHA KNOCKOUT MICE
    WANG, ND
    FINEGOLD, MJ
    BRADLEY, A
    OU, CN
    ABDELSAYED, SV
    WILDE, MD
    TAYLOR, LR
    WILSON, DR
    DARLINGTON, GJ
    [J]. SCIENCE, 1995, 269 (5227) : 1108 - 1112
  • [38] Targeted in vivo expression of the cyclin-dependent kinase inhibitor p21 halts hepatocyte cell-cycle progression, postnatal liver development, and regeneration
    Wu, H
    Wade, M
    Krall, L
    Grisham, J
    Xiong, Y
    VanDyke, T
    [J]. GENES & DEVELOPMENT, 1996, 10 (03) : 245 - 260
  • [39] Absence of granulocyte colony-stimulating factor signaling and neutrophil development in CCAAT enhancer binding protein alpha-deficient mice
    Zhang, DE
    Zhang, P
    Wang, ND
    Hetherington, CJ
    Darlington, GJ
    Tenen, DG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (02) : 569 - 574
  • [40] E2F3 contributes both to the inappropriate proliferation and to the apoptosis arising in Rb mutant embryos
    Ziebold, U
    Reza, T
    Caron, A
    Lees, JA
    [J]. GENES & DEVELOPMENT, 2001, 15 (04) : 386 - 391