Transcriptional control of SPARC by v-Jun and other members of the AP1 family of transcription factors

被引:34
作者
Vial, E [1 ]
Perez, S [1 ]
Castellazzi, M [1 ]
机构
[1] Ecole Normale Super Lyon, INSERM, U412, Unite Virol Humaine, F-69364 Lyon 07, France
关键词
v-Jun; Fra2; ATF2; Maf; AP1; SPARC promoter; chick embryo fibroblasts; cell transformation;
D O I
10.1038/sj.onc.1203867
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
Transformation of chick embryo fibroblasts by the v-Jun oncoprotein correlates with a down-regulation of the extracellular matrix protein SPARC and repression of the corresponding mRNA, Alteration in SPARC expression has been repeatedly reported in human cancers of various origin, and is thought to contribute to the remodeling of the extracellular matrix during neoplastic progression, Transcriptional control of SPARC is poorly understood, We show here that (i) v-Jun-mediated repression of the endogenous SPARC gene is enhanced by Fra2 but alleviated by ATF2, Fra2 and ATF2 being the two major partners of v-Jun in the transformed cells; (ii) high basal activity as well as repression by v-Jun and modulation by Fra2 and ATF2 is restricted to a small proximal fragment (-124/+16) of the chicken SPARC promoter; (iii) the activity of this minimal promoter is modulated by all the AP1 family members known in chickens (c-Jun and JunD; c-Fos and Fra2; ATF2; c-Maf, MafA, and MafB), Taken together these data demonstrate that, at least in avian primary cells, SPARC expression is under the control of the AP1 transcription factor. Further studies with the minimal (-124/+16) promoter fragment are needed to understand how this control takes place at the molecular level.
引用
收藏
页码:5020 / 5029
页数:10
相关论文
共 48 条
[1]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[2]  
BENJAMIN T, 1990, VIROLOGY, V1, P317
[3]   mafA, a novel member of the maf proto-oncogene family, displays developmental regulation and mitogenic capacity in avian neuroretina cells [J].
Benkhelifa, S ;
Provot, S ;
Lecoq, O ;
Pouponnot, C ;
Calothy, G ;
Felder-Schmittbuhl, MP .
ONCOGENE, 1998, 17 (02) :247-254
[4]   DIVERSITY OF FUNCTION IS INHERENT IN MATRICELLULAR PROTEINS - AN APPRAISAL OF THROMBOSPONDIN-1 [J].
BORNSTEIN, P .
JOURNAL OF CELL BIOLOGY, 1995, 130 (03) :503-506
[5]  
CASTELLAZZI M, 1990, ONCOGENE, V5, P1541
[6]   The Wilms' tumor gene product represses the transcription of thrombospondin 1 in response to overexpression of c-Jun [J].
Dejong, V ;
Degeorges, A ;
Filleur, S ;
Ait-Si-Ali, S ;
Mettouchi, A ;
Bornstein, P ;
Binétruy, B ;
Cabon, F .
ONCOGENE, 1999, 18 (20) :3143-3151
[7]   PURIFICATION AND TISSUE DISTRIBUTION OF A SMALL PROTEIN (BM-40) EXTRACTED FROM A BASEMENT-MEMBRANE TUMOR [J].
DZIADEK, M ;
PAULSSON, M ;
AUMAILLEY, M ;
TIMPL, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 161 (02) :455-464
[8]  
Gao MH, 1996, CANCER RES, V56, P4229
[9]   Expression of osteonectin mRNA in human breast tumours is inversely correlated with oestrogen receptor content [J].
Graham, JD ;
Balleine, RL ;
Milliken, JS ;
Bilous, AM ;
Clarke, CL .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (10) :1654-1660
[10]   A purine-rich sequence in the human BM-40 gene promoter region is a prerequisite for maximum transcription [J].
Hafner, M ;
Zimmermann, K ;
Pottgiesser, J ;
Krieg, T ;
Nischt, R .
MATRIX BIOLOGY, 1995, 14 (09) :733-741