WW domain-containing FBP-30 is regulated by p53

被引:8
作者
Depraetere, V [1 ]
Golstein, P [1 ]
机构
[1] CNRS Marseille Luminy, Ctr Immunol, INSERM, F-13288 Marseille 9, France
关键词
gamma-irradiation; p53; subtractive cloning; FBP-30; WW domain;
D O I
10.1038/sj.cdd.4400564
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
A subtractive cloning approach was used to clone genes transcriptionally induced in thymocytes undergoing programmed cell death after gamma-irradiation. We thus identified about 60 upregulated genes. One of these genes encodes a WW domain previously briefly reported by others, which defines this gene as FBP-30. cDNA sequencing showed FBP-30 to be remarkably conserved in mammals. FBP-30 expression, essentially restricted to T cells, was regulated by p53 since it increased (1) after gamma-irradiation in wild-type but not in p53 -/- thymocytes and (2) in cells transfected with a conditional temperature-sensitive p53 mutant, less than 1 h after shifting to permissive temperature. Upregulation of FBP-30 expression thus depends upon p53 protein expression and correlates with cell death induction in these systems. While the kinetics of its induction are rapid, the observed increased expression of FBP-30 in the presence of protein synthesis inhibitors suggests that FBP-30 gene expression is indirectly regulated by p53, through downregulation of a labile inhibitor of FBP-30 expression.
引用
收藏
页码:883 / 889
页数:7
相关论文
共 44 条
[1]
BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]
Isolation of 10 differentially expressed cDNAs in p53-induced apoptosis: Activation of the vertebrate homologue of the Drosophila seven in absentia gene [J].
Amson, RB ;
Nemani, M ;
Roperch, JP ;
Israeli, D ;
Bougueleret, L ;
LeGall, I ;
Medhioub, M ;
LinaresCruz, G ;
Lethrosne, F ;
Pasturaud, P ;
Piouffre, L ;
Prieur, S ;
Susini, L ;
Alvaro, V ;
Millasseau, P ;
Guidicelli, C ;
Bui, H ;
Massart, C ;
Cazes, L ;
Dufour, F ;
BruzzoniGiovanelli, H ;
Owadi, H ;
Hennion, C ;
Charpak, G ;
Dausset, J ;
Calvo, F ;
Oren, M ;
Cohen, D ;
Telerman, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :3953-3957
[3]
Multiplex messenger assay: Simultaneous, quantitative measurement of expression of many genes in the context of T cell activation [J].
Bernard, K ;
Auphan, N ;
Granjeaud, S ;
Victorero, G ;
SchmittVerhulst, AM ;
Jordan, BR ;
Nguyen, C .
NUCLEIC ACIDS RESEARCH, 1996, 24 (08) :1435-1442
[4]
FC RECEPTOR STIMULATION OF PHOSPHATIDYLINOSITOL 3-KINASE IN NATURAL-KILLER-CELLS IS ASSOCIATED WITH PROTEIN-KINASE C-INDEPENDENT GRANULE RELEASE AND CELL-MEDIATED CYTOTOXICITY [J].
BONNEMA, JD ;
KARNITZ, LM ;
SCHOON, RA ;
ABRAHAM, RT ;
LEIBSON, PJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1427-1435
[5]
THE WW DOMAIN - A SIGNALING SITE IN DYSTROPHIN [J].
BORK, P ;
SUDOL, M .
TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (12) :531-533
[6]
Deletion of the mouse T-cell receptor beta gene enhancer blocks alpha beta T-cell development [J].
Bouvier, G ;
Watrin, F ;
Naspetti, M ;
Verthuy, C ;
Naquet, P ;
Ferrier, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7877-7881
[7]
CASTRILLON DH, 1994, DEVELOPMENT, V120, P3367
[8]
Genetic evidence that formins function within the nucleus [J].
Chan, DC ;
Leder, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (38) :23472-23477
[9]
CHAN DC, 1995, DEVELOPMENT, V121, P3151
[10]
THYMOCYTE APOPTOSIS INDUCED BY P53-DEPENDENT AND INDEPENDENT PATHWAYS [J].
CLARKE, AR ;
PURDIE, CA ;
HARRISON, DJ ;
MORRIS, RG ;
BIRD, CC ;
HOOPER, ML ;
WYLLIE, AH .
NATURE, 1993, 362 (6423) :849-852