Cloning and characterization of GETS-1, a goldfish Ets family member that functions as a transcriptional repressor in muscle

被引:14
作者
Goldman, D
Sapru, MK
Stewart, S
Plotkin, J
Libermann, TA
Wasylyk, B
Guan, K
机构
[1] Univ Michigan, Mental Hlth Res Inst, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
[3] Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Boston, MA 02215 USA
[5] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch, France
[6] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1042/bj3350267
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
An Ets transcription factor family member, GETS-1, was cloned from a goldfish retina cDNA library. GETS-1 contains a conserved Ets DNA-binding domain at its N-terminus and is most similar to ternary complex factor (TCF) serum-response-factor protein-1a (SAP-1a). GETS-1 is expressed in many tissues, but is enriched in retina and brain. As with the TCFs SAP-1a and ets-related protein (ERP), overexpression of the GETS-1 promoter suppresses nicotinic acetylcholine receptor epsilon-subunit gene expression in cultured muscle cells. A consensus Ets binding site sequence in the promoter of the epsilon-subunit gene is required for GETS-1-mediated repression. GETS-1 repressor activity is abrogated by overexpression of an activated Ras/mitogen-activated protein kinase (MAP kinase) or by mutation of Ser-405, a MAP kinase phosphorylation site in GETS-1. Fusion proteins created between GETS-1 and the Gal4 DNA-binding domain show that, like other TCFs, GETS-1 contains a C-terminal activation domain that is activated by a Ras/MAP kinase signalling cascade. Interestingly, mutation of Ser-405 located within this activation domain abrogated transcriptional activation of the fusion protein.
引用
收藏
页码:267 / 275
页数:9
相关论文
共 50 条
[1]   ELF-1 interacts with and transactivates the IgH enhancer pi site [J].
Akbarali, Y ;
Oettgen, P ;
Boltax, J ;
Libermann, TA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (42) :26007-26012
[2]  
ALVAREZ E, 1991, J BIOL CHEM, V266, P15277
[3]  
BRASIER AR, 1989, BIOTECHNIQUES, V7, P1116
[4]  
CHAHINE KG, 1993, J BIOL CHEM, V268, P2893
[5]   ACTIVATION OF MAP KINASE KINASE IS NECESSARY AND SUFFICIENT FOR PC12 DIFFERENTIATION AND FOR TRANSFORMATION OF NIH 3T3 CELLS [J].
COWLEY, S ;
PATERSON, H ;
KEMP, P ;
MARSHALL, CJ .
CELL, 1994, 77 (06) :841-852
[6]   CHARACTERIZATION OF SAP-1, A PROTEIN RECRUITED BY SERUM RESPONSE FACTOR TO THE C-FOS SERUM RESPONSE ELEMENT [J].
DALTON, S ;
TREISMAN, R .
CELL, 1992, 68 (03) :597-612
[7]   MEKKs, GCKs, MLKs, PAKs, TAKs, and Tpls: Upstream regulators of the c-Jun amino-terminal kinases? [J].
Fanger, GR ;
Gerwins, P ;
Widmann, C ;
Jarpe, MB ;
Johnson, GL .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1997, 7 (01) :67-74
[8]   ELECTRICAL-ACTIVITY SUPPRESSES NICOTINIC ACETYLCHOLINE-RECEPTOR GAMMA-SUBUNIT PROMOTER ACTIVITY [J].
GILMOUR, BP ;
GOLDMAN, D ;
CHAHINE, KG ;
GARDNER, PD .
DEVELOPMENTAL BIOLOGY, 1995, 168 (02) :416-428
[9]   EUKARYOTIC PROTEINS EXPRESSED IN ESCHERICHIA-COLI - AN IMPROVED THROMBIN CLEAVAGE AND PURIFICATION PROCEDURE OF FUSION PROTEINS WITH GLUTATHIONE-S-TRANSFERASE [J].
GUAN, KL ;
DIXON, JE .
ANALYTICAL BIOCHEMISTRY, 1991, 192 (02) :262-267
[10]  
HIEBER V, 1993, METHODS NEUROSCI, V12, P122