Signal-specific co-activator domain requirements for Pit-1 activation

被引:0
|
作者
Lan Xu
Robert M. Lavinsky
Jeremy S. Dasen
Sarah E. Flynn
Eileen M. McInerney
Tina-Marie Mullen
Thorsten Heinzel
Daniel Szeto
Edward Korzus
Riki Kurokawa
Aneel K. Aggarwal
David W. Rose
Christopher K. Glass
Michael G. Rosenfeld
机构
[1] Howard Hughes Medical Institute,Department of Biology Graduate Program
[2] University of California at San Diego,Department and School of Medicine
[3] Biomedical Sciences Graduate Program,Department of Physiology and Biophysics
[4] University of California at San Diego,undefined
[5] University of California at San Diego,undefined
[6] Whittier Diabetes Program,undefined
[7] University of California at San Diego,undefined
[8] Cellular and Molecular Medicine,undefined
[9] and University of California at San Diego,undefined
[10] University of California at San Diego,undefined
[11] Mount Sinai School of Medicine,undefined
来源
Nature | 1998年 / 395卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
POU-domain proteins, such as the pituitary-specific factor Pit-1, are members of the homeodomain family of proteins which are important in development and homeostasis, acting constitutively or in response to signal-transduction pathways to either repress or activate the expression of specific genes1. Here we show that whereas homeodomain-containing repressors such as Rpx2 seem to recruit only a co-repressor complex, the activity of Pit-1 (ref. 3) is determined by a regulated balance between a co-repressor complex that contains N-CoR/SMRT4,5, mSin3A/B6,7,8 and histone deacetylases6,7,8 and a co-activator complex that includes the CREB-binding protein (CBP)9 and p/CAF10. Activation of Pit-1 by cyclic AMP or growth factors depends on distinct amino- and carboxy-terminal domains of CBP, respectively. Furthermore, thehistone acetyltransferase functions of CBP11,12 or p/CAF10 are required for Pit-1 function that is stimulated by cyclic AMP or growth factors, respectively. These data show that there is a switch in specific requirements for histone acetyltransferases and CBP domains in mediating the effects of different signal-transduction pathways on specific DNA-bound transcription factors.
引用
收藏
页码:301 / 306
页数:5
相关论文
共 50 条
  • [41] Two variants of the pituitary specific transcription factor Pit-1 in Atlantic salmon
    Lorens, JB
    Aasland, R
    Brunstad, H
    Bergh, H
    Male, R
    JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1996, 17 (03) : 225 - 236
  • [42] A TISSUE-SPECIFIC ENHANCER CONFERS PIT-1-DEPENDENT MORPHOGEN INDUCIBILITY AND AUTOREGULATION ON THE PIT-1 GENE
    RHODES, SJ
    CHEN, RP
    DIMATTIA, GE
    SCULLY, KM
    KALLA, KA
    LIN, SC
    YU, VC
    ROSENFELD, MG
    GENES & DEVELOPMENT, 1993, 7 (06) : 913 - 932
  • [43] PIT-1 BINDING TO SPECIFIC DNA SITES AS A MONOMER OR DIMER DETERMINES GENE-SPECIFIC USE OF A TYROSINE-DEPENDENT SYNERGY DOMAIN
    HOLLOWAY, JM
    SZETO, DP
    SCULLY, KM
    GLASS, CK
    ROSENFELD, MG
    GENES & DEVELOPMENT, 1995, 9 (16) : 1992 - 2006
  • [44] Identification of a co-activator that links growth factor signalling to c-Jun/AP-1 activation
    Davies, Clare C.
    Chakraborty, Atanu
    Cipriani, Filippo
    Haigh, Katharina
    Haigh, Jody J.
    Behrens, Axel
    NATURE CELL BIOLOGY, 2010, 12 (10) : 963 - 972
  • [45] Identification of the transactivation domain of the transcription factor Sox-2 and an associated co-activator
    Nowling, TK
    Johnson, LR
    Wiebe, MS
    Rizzino, A
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (06) : 3810 - 3818
  • [46] Identification of a co-activator that links growth factor signalling to c-Jun/AP-1 activation
    Clare C. Davies
    Atanu Chakraborty
    Filippo Cipriani
    Katharina Haigh
    Jody J. Haigh
    Axel Behrens
    Nature Cell Biology, 2010, 12 : 963 - 972
  • [47] AXIN is an essential co-activator for the promyelocytic leukemia protein in p53 activation
    Li, Q.
    He, Y.
    Wei, L.
    Wu, X.
    Wu, D.
    Lin, S.
    Wang, Z.
    Ye, Z.
    Lin, S-C
    ONCOGENE, 2011, 30 (10) : 1194 - 1204
  • [48] Identification of non-functional mutations in the Pit-1 POU-specific domain that cause altered subnuclear partitioning.
    Ouspenski, II
    Mancini, MG
    Brown, C
    Sharp, ZD
    Mancini, MA
    MOLECULAR BIOLOGY OF THE CELL, 1996, 7 : 2713 - 2713
  • [49] Identification of MP-1, a novel co-activator of MEK.
    Catling, AD
    Schaeffer, HJ
    Collier, L
    Krauss, A
    Weber, MJ
    FASEB JOURNAL, 1997, 11 (09): : A1333 - A1333
  • [50] Regulation of the expression of HMG1, a co-activator of the estrogen receptor
    Borrmann, L
    Kim, I
    Schultheiss, D
    Rogalla, P
    Bullerdiek, J
    ANTICANCER RESEARCH, 2001, 21 (1A) : 301 - 305