Transcriptional regulation by steroid receptor coactivator phosphorylation

被引:128
作者
Wu, RC [1 ]
Smith, CL [1 ]
O'Malley, BW [1 ]
机构
[1] Baylor Coll Med, Houston, TX 77030 USA
关键词
D O I
10.1210/er.2004-0018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The basic mechanisms underlying ligand-dependent transcriptional activation by nuclear receptors (NRs) require the sequential recruitment of various coactivators. Increasing numbers of coactivators have been identified in recent years, and both biochemical and genetic studies demonstrate that these coactivators are differentially used by transcription factors, including NRs, in a cell/tissue type- and promoter-specific manner. However, the molecular basis underlying this specificity remains largely unknown. Recently, NRs and coregulators were shown to be targets of posttranslational modifications activated by diverse cellular signaling pathways. It is argued that posttranslational modifications of these proteins provide the basis for a combinatorial code required for specific gene activation by NRs and coactivators, and that this code also enables coactivators to efficiently stimulate the activity of other classes of transcription factors. In this review, we will focus on coactivators and discuss the recent progress in understanding the role of phosphorylation of the steroid receptor coactivator family and the potential ramifications of this posttranslational modification for regulation of gene expression.
引用
收藏
页码:393 / 399
页数:7
相关论文
共 70 条
[21]   The partial agonist activity of antagonist-occupied steroid receptors is controlled by a novel hinge domain-binding coactivator L7/SPA and the corepressors N-CoR or SMRT [J].
Jackson, TA ;
Richer, JK ;
Bain, DL ;
Takimoto, GS ;
Tung, L ;
Horwitz, KB .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (06) :693-705
[22]   Combinatorial roles of the nuclear receptor corepressor in transcription and development [J].
Jepsen, K ;
Hermanson, O ;
Onami, TM ;
Gleiberman, AS ;
Lunyak, V ;
McEvilly, RJ ;
Kurokawa, R ;
Kumar, V ;
Liu, F ;
Seto, E ;
Hedrick, SM ;
Mandel, G ;
Glass, CK ;
Rose, DW ;
Rosenfeld, MG .
CELL, 2000, 102 (06) :753-763
[23]   ACTIVATION OF THE ESTROGEN-RECEPTOR THROUGH PHOSPHORYLATION BY MITOGEN-ACTIVATED PROTEIN-KINASE [J].
KATO, S ;
ENDOH, H ;
MASUHIRO, Y ;
KITAMOTO, T ;
UCHIYAMA, S ;
SASAKI, H ;
MASUSHIGE, S ;
GOTOH, Y ;
NISHIDA, E ;
KAWASHIMA, H ;
METZGER, D ;
CHAMBON, P .
SCIENCE, 1995, 270 (5241) :1491-1494
[24]   The nuclear receptor interaction domain of GRIP1 is modulated by covalent attachment of SUMO-1 [J].
Kotaja, N ;
Karvonen, U ;
Jänne, OA ;
Palvimo, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (33) :30283-30288
[25]   AIB1/SRC-3 deficiency affects insulin-like growth factor I signaling pathway and suppresses v-Ha-ras-induced breast cancer initiation and progression in mice [J].
Kuang, SQ ;
Liao, L ;
Zhang, H ;
Lee, AV ;
O'Malley, BW ;
Xu, JM .
CANCER RESEARCH, 2004, 64 (05) :1875-1885
[26]   Differential use of CREB binding protein coactivator complexes [J].
Kurokawa, R ;
Kalafus, D ;
Ogliastro, MH ;
Kioussi, C ;
Xu, L ;
Torchia, J ;
Rosenfeld, MG ;
Glass, CK .
SCIENCE, 1998, 279 (5351) :700-703
[27]   Estrogen receptor phosphorylation [J].
Lannigan, DA .
STEROIDS, 2003, 68 (01) :1-9
[28]   Diverse signaling pathways modulate nuclear receptor recruitment of N-CoR and SMRT complexes [J].
Lavinsky, RM ;
Jepsen, K ;
Heinzel, T ;
Torchia, J ;
Mullen, TM ;
Schiff, R ;
Del-Rio, AL ;
Ricote, M ;
Ngo, S ;
Gemsch, J ;
Hilsenbeck, SG ;
Osborne, CK ;
Glass, CK ;
Rosenfeld, MG ;
Rose, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :2920-2925
[29]  
LE GP, 1994, J BIOL CHEM, V269, P4458
[30]   Steroid receptor coactivator-1 and its family members differentially regulate transactivation by the tumor suppressor protein p53 [J].
Lee, SK ;
Kim, HJ ;
Kim, JW ;
Lee, JW .
MOLECULAR ENDOCRINOLOGY, 1999, 13 (11) :1924-1933