Ets ternary complex transcription factors

被引:299
作者
Buchwalter, G [1 ]
Gross, C [1 ]
Wasylyk, B [1 ]
机构
[1] INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, ULP, F-67404 Illkirch Graffenstaden, France
关键词
Elk-1; Elk-3; Elk-4; Net; Erp; Sap-1; Sap-2; SRF; MAP kinase; phosphorylation; immediate early genes;
D O I
10.1016/j.gene.2003.09.028
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The three ternary complex factors (TCFs) Elk-1, Net and Sap-1 form a subfamily of the E twenty-six (Ets) domain transcription factors. Their characteristic property is the ability to form a ternary nucleoprotein complex with the serum response factor (SRF) over the serum response element (SRE) of the c-fos promoter. The molecular mechanisms that underlie the function and regulation of these factors have been response element (SRE) of the extensively studied and the TCFs are a paradigm for the study of transcriptional regulation in response to extracellular signalling through the mitogen-activated protein (MA-P) kinase pathway. As final effectors of multiple signalling pathways and components of protein complexes on immediate early promoters, they represent key elements in the complex and dynamic regulation of gene expression. This review summarises the molecular, structural and biochemical studies that have led to the understanding of the functional domains of the TCFs, ternary complex formation, transcriptional regulation, protein partners and target genes in cell lines. Finally, the emerging studies of the biological roles of the TCFs in vivo will be discussed. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 125 条
[81]   ELK, TISSUE-SPECIFIC ETS-RELATED GENES ON CHROMOSOME-X AND CHROMOSOME-14 NEAR TRANSLOCATION BREAKPOINTS [J].
RAO, VN ;
HUEBNER, K ;
ISOBE, M ;
ARRUSHDI, A ;
CROCE, CM ;
REDDY, ESP .
SCIENCE, 1989, 244 (4900) :66-70
[82]  
RAO VN, 1993, CANCER RES, V53, P215
[83]   Mitogen-activated protein kinase pathways [J].
Robinson, MJ ;
Cobb, MH .
CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (02) :180-186
[84]   Role of ETS family transcription factors in vascular development and angiogenesis [J].
Sato, Y .
CELL STRUCTURE AND FUNCTION, 2001, 26 (01) :19-24
[85]   MOLECULAR-CLONING AND CHARACTERIZATION OF A CELLULAR PHOSPHOPROTEIN THAT INTERACTS WITH A CONSERVED C-TERMINAL DOMAIN OF ADENOVIRUS E1A INVOLVED IN NEGATIVE MODULATION OF ONCOGENIC TRANSFORMATION [J].
SCHAEPER, U ;
BOYD, JM ;
VERMA, S ;
UHLMANN, E ;
SUBRAMANIAN, T ;
CHINADURAI, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) :10467-10471
[86]   Serum response factor is required for immediate-early gene activation yet is dispensable for proliferation of embryonic stem cells [J].
Schratt, G ;
Weinhold, B ;
Lundberg, AS ;
Schuck, S ;
Berger, J ;
Schwarz, H ;
Weinberg, RA ;
Rüther, U ;
Nordheim, A .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (08) :2933-2943
[87]  
Sgambato V, 1998, J NEUROSCI, V18, P214
[88]   ERF - AN ETS DOMAIN PROTEIN WITH STRONG TRANSCRIPTIONAL REPRESSOR ACTIVITY, CAN SUPPRESS ETS-ASSOCIATED TUMORIGENESIS AND IS REGULATED BY PHOSPHORYLATION DURING CELL-CYCLE AND MITOGENIC STIMULATION [J].
SGOURAS, DN ;
ATHANASIOU, MA ;
BEAL, GJ ;
FISHER, RJ ;
BLAIR, DG ;
MAVROTHALASSITIS, GJ .
EMBO JOURNAL, 1995, 14 (19) :4781-4793
[89]   Docking domains and substrate-specificity determination for MAP kinases [J].
Sharrocks, AD ;
Yang, SH ;
Galanis, A .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (09) :448-453
[90]  
Sharrocks AD, 2002, BIOCHEM SOC T, V30, P1