Role of the Fos family members, c-Fos, Fra-1 and Fra-2, in the regulation of cell motility

被引:61
作者
Tkach, V
Tulchinsky, E
Lukanidin, E
Vinson, C
Bock, E
Berezin, V
机构
[1] Univ Copenhagen, Panum Inst, Prot Lab,Inst Mol Pathol, Sch Med, DK-2200 Copenhagen N, Denmark
[2] Danish Canc Soc, Dept Mol Cell Biol, Inst Canc Biol, DK-2100 Copenhagen O, Denmark
[3] NCI, Met Lab, NIH, Bethesda, MD 20892 USA
关键词
c-Fos; Fra-1; Fra-2; cell locomotion;
D O I
10.1038/sj.onc.1206570
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
The AP-1 transcription factor is composed of members of the Fos, Jun and ATF families, and plays a key role in tumor progression. We investigated whether Fos proteins regulate cell motility, and if so, whether this capacity is related to their transactivation potential. Two cell tines with different expression profiles of AP-1 were employed focusing on the Fos-family members c-Fos, Fra-1 and Fra-2. Transactivation motifs are found in c-Fos, but not in Fra-1 or Fra-2. The adenocarcinoma CSML0 cells display a low motility and do not express Fra-1 or Fra-2, and only very little c-Fos. In contrast, the fibroblastoid L929 cells express both Fra-1 and Fra-2, but no c-Fos, and these cells display a high motility. Transfection with Fra-1 or c-Fos, but not with Fra-2, strongly enhanced the motility of CSML0 cells. The effect of Fra-1 required the presence of the N-terminal domain of this protein. Conversely, transfection with a Fos dominant-negative mutant or with anti-sense fra-1 or fra-2, strongly reduced the motility of L929 cells. Changes in cell motility correlated with the morphological appearance and the degree of contact with the substratum. We conclude that Fos proteins have distinct roles in the regulation of cell motility.
引用
收藏
页码:5045 / 5054
页数:10
相关论文
共 29 条
[1]   The transcription factor Fos-related antigen 1 is induced by thiazolidinediones during differentiation of 3T3-L1 cells [J].
Albrektsen, T ;
Fleckner, J .
MOLECULAR PHARMACOLOGY, 2001, 59 (03) :567-575
[2]   The ability of Fos family members to produce phenotypic changes in epithelioid cells is not directly linked to their transactivation potentials [J].
Andersen, H ;
Mahmood, S ;
Tkach, V ;
Cohn, M ;
Kustikova, O ;
Grigorian, M ;
Berezin, V ;
Bock, E ;
Lukanidin, E ;
Tulchinsky, E .
ONCOGENE, 2002, 21 (31) :4843-4848
[3]  
BERGERS G, 1995, MOL CELL BIOL, V15, P3748
[4]   MAXIMAL MIGRATION OF HUMAN SMOOTH-MUSCLE CELLS ON FIBRONECTIN AND TYPE-IV COLLAGEN OCCURS AT AN INTERMEDIATE ATTACHMENT STRENGTH [J].
DIMILLA, PA ;
STONE, JA ;
QUINN, JA ;
ALBELDA, SM ;
LAUFFENBURGER, DA .
JOURNAL OF CELL BIOLOGY, 1993, 122 (03) :729-737
[5]  
Dunn G A, 1983, Agents Actions Suppl, V12, P14
[6]   A novel, transformation-relevant activation domain in Fos proteins [J].
Funk, M ;
Poensgen, B ;
Graulich, W ;
Jerome, V ;
Muller, R .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (02) :537-544
[7]   CROSS-FAMILY DIMERIZATION OF TRANSCRIPTION FACTORS FOS JUN AND ATF CREB ALTERS DNA-BINDING SPECIFICITY [J].
HAI, T ;
CURRAN, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3720-3724
[8]   CHARACTERIZATION OF JUND - A NEW MEMBER OF THE JUN PROTO-ONCOGENE FAMILY [J].
HIRAI, SI ;
RYSECK, RP ;
MECHTA, F ;
BRAVO, R ;
YANIV, M .
EMBO JOURNAL, 1989, 8 (05) :1433-1439
[9]   THE T-CELL TRANSCRIPTION FACTOR NFAT(P) IS A SUBSTRATE FOR CALCINEURIN AND INTERACTS WITH FOS AND JUN [J].
JAIN, JN ;
MCCAFFREY, PG ;
MINER, Z ;
KERPPOLA, TK ;
LAMBERT, JN ;
VERDINE, GL ;
CURRAN, T ;
RAO, A .
NATURE, 1993, 365 (6444) :352-355
[10]   Tumor invasion as dysregulated cell motility [J].
Kassis, J ;
Lauffenburger, DA ;
Turner, T ;
Wells, A .
SEMINARS IN CANCER BIOLOGY, 2001, 11 (02) :105-117