Identification of a c-fos-induced gene that is related to the platelet-derived growth factor vascular endothelial growth factor family

被引:257
作者
Orlandini, M [1 ]
Marconcini, L [1 ]
Ferruzzi, R [1 ]
Oliviero, S [1 ]
机构
[1] UNIV SIENA,CTR RIC,IRIS,DIPARTIMENTO BIOL MOL,I-53100 SIENA,ITALY
关键词
Fos; cell transformation;
D O I
10.1073/pnas.93.21.11675
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Using a mRNA differential screening of fibroblasts differing for the expression of c-fos we isolated a c-fos-induced growth factor (FIGF). The deduced protein sequence predicts that the cDNA codes for a new member of the platelet-derived growth factor/vascular endothelial growth factor (PDGF/VEGF) family. Northern blot analysis shows that FIGF expression is strongly reduced in c-fos-deficient cells. Transfection of exogenous c-fos driven by a constitutive promoter restores the FIGF expression in these cells. In contrast, both PDGF and VEGF expression is unaffected by c-fos. FIGF is a secreted dimeric protein able to stimulate mitogenic activity in fibroblasts. FIGF overexpression induces morphological alterations in fibroblasts. The cells acquire a spindle-shaped morphology, become more refractive, disorganized, and detach from the plate. These results imply that FIGF is a downstream growth and morphogenic effector of c-fos. These results also suggest that the expression of FIGF in response to c-fos activation induces specific differentiation patterns and its aberrant activation contributes to the malignant phenotype of tumors.
引用
收藏
页码:11675 / 11680
页数:6
相关论文
共 36 条
[1]  
ANDERSSON M, 1992, J BIOL CHEM, V267, P11260
[2]   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
[3]   IDENTIFICATION OF DIFFERENTIALLY EXPRESSED MESSENGER-RNA SPECIES BY AN IMPROVED DISPLAY TECHNIQUE (DDRT-PCR) [J].
BAUER, D ;
MULLER, H ;
REICH, J ;
RIEDEL, H ;
AHRENKIEL, V ;
WARTHOE, P ;
STRAUSS, M .
NUCLEIC ACIDS RESEARCH, 1993, 21 (18) :4272-4280
[4]   CDNA SEQUENCE AND CHROMOSOMAL LOCALIZATION OF HUMAN PLATELET-DERIVED GROWTH-FACTOR A-CHAIN AND ITS EXPRESSION IN TUMOR-CELL LINES [J].
BETSHOLTZ, C ;
JOHNSSON, A ;
HELDIN, CH ;
WESTERMARK, B ;
LIND, P ;
URDEA, MS ;
EDDY, R ;
SHOWS, TB ;
PHILPOTT, K ;
MELLOR, AL ;
KNOTT, TJ ;
SCOTT, J .
NATURE, 1986, 320 (6064) :695-699
[5]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[6]  
CLAFFEY KP, 1992, J BIOL CHEM, V267, P16317
[7]   NUCLEOPROTEIN COMPLEXES THAT REGULATE GENE-EXPRESSION IN ADIPOCYTE DIFFERENTIATION - DIRECT PARTICIPATION OF C-FOS [J].
DISTEL, RJ ;
RO, HS ;
ROSEN, BS ;
GROVES, DL ;
SPIEGELMAN, BM .
CELL, 1987, 49 (06) :835-844
[8]   FOS AND BONE CELL-DEVELOPMENT - LESSONS FROM A NUCLEAR ONCOGENE [J].
GRIGORIADIS, AE ;
WANG, ZQ ;
WAGNER, EF .
TRENDS IN GENETICS, 1995, 11 (11) :436-441
[9]   PREPARATION OF BIOLOGICALLY-ACTIVE PLATELET-DERIVED GROWTH-FACTOR TYPE-BB FROM A FUSION PROTEIN EXPRESSED IN ESCHERICHIA-COLI [J].
HOPPE, J ;
WEICH, HA ;
EICHNER, W .
BIOCHEMISTRY, 1989, 28 (07) :2956-2960
[10]   PREPARATION OF BIOLOGICALLY-ACTIVE PLATELET-DERIVED GROWTH-FACTOR ISOFORMS AA AND AB - PREFERENTIAL FORMATION OF AB HETERODIMERS [J].
HOPPE, J ;
WEICH, HA ;
EICHNER, W ;
TATJE, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 187 (01) :207-214