Crk is required for apoptosis in Xenopus egg extracts

被引:50
作者
Evans, EK
Lu, W
Strum, SL
Mayer, BJ
Kornbluth, S
机构
[1] DUKE UNIV, MED CTR, DEPT MOL CANC BIOL, DURHAM, NC 27710 USA
[2] HARVARD UNIV, CHILDRENS HOSP, HOWARD HUGHES MED INST, BOSTON, MA 02115 USA
[3] HARVARD UNIV, SCH MED, DEPT MICROBIOL & MOL GENET, BOSTON, MA 02115 USA
关键词
apoptosis; crk protein; signaling; Xenopus;
D O I
10.1093/emboj/16.2.230
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
Apoptosis is essential for the development and homeostasis of multicellular organisms, Recently, a cell-free extract prepared from Xenopus eggs was shown to recapitulate intracellular apoptotic pathways in vitro, While many stimuli have been shown to trigger apoptosis in a variety of cell types, the intracellular signaling pathways involved in apoptosis remain largely unknown, Here we show that addition of a recombinant protein containing the phosphotyrosine binding (SH2) domain from the adaptor protein crk, but not those derived from a panel of other signaling proteins, call prevent apoptosis in the Xenopus egg extract system. Furthermore, immunodepletion of endogenous crk protein from the egg extracts, or addition of anti-crk antisera to these extracts, prevents apoptosis. The ability to undergo apoptosis can be restored to these extracts by addition of recombinant crk protein. These results directly demonstrate that crk participates in apoptotic signaling.
引用
收藏
页码:230 / 241
页数:12
相关论文
共 53 条
[1]   CLONING THE CHROMOSOMAL BREAKPOINT OF T(14-18) HUMAN LYMPHOMAS - CLUSTERING AROUND JH ON CHROMOSOME-14 AND NEAR A TRANSCRIPTIONAL UNIT ON 18 [J].
BAKHSHI, A ;
JENSEN, JP ;
GOLDMAN, P ;
WRIGHT, JJ ;
MCBRIDE, OW ;
EPSTEIN, AL ;
KORSMEYER, SJ .
CELL, 1985, 41 (03) :899-906
[2]   CELL-DEATH IN HEALTH AND DISEASE - THE BIOLOGY AND REGULATION OF APOPTOSIS [J].
BELLAMY, COC ;
MALCOMSON, RDG ;
HARRISON, DJ ;
WYLLIE, AH .
SEMINARS IN CANCER BIOLOGY, 1995, 6 (01) :3-16
[3]   IDENTIFICATION AND CHARACTERIZATION OF A HIGH-AFFINITY INTERACTION BETWEEN V-CRK AND TYROSINE-PHOSPHORYLATED PAXILLIN IN CT10-TRANSFORMED FIBROBLASTS [J].
BIRGE, RB ;
FAJARDO, JE ;
REICHMAN, C ;
SHOELSON, SE ;
SONGYANG, Z ;
CANTLEY, LC ;
HANAFUSA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (08) :4648-4656
[4]   Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death [J].
Boldin, MP ;
Goncharov, TM ;
Goltsev, YV ;
Wallach, D .
CELL, 1996, 85 (06) :803-815
[5]  
CHAPMAN RS, 1994, CANCER RES, V54, P5131
[6]  
Chinnaiyan AM, 1996, CURR BIOL, V6, P555
[7]   INDUCTION OF APOPTOSIS BY THE BCL-2 HOMOLOG BAK [J].
CHITTENDEN, T ;
HARRINGTON, EA ;
OCONNOR, R ;
FLEMINGTON, C ;
LUTZ, RJ ;
EVAN, GI ;
GUILD, BC .
NATURE, 1995, 374 (6524) :733-736
[8]   CLONING AND STRUCTURAL-ANALYSIS OF CDNAS FOR BCL-2 AND A HYBRID BCL-2/IMMUNOGLOBULIN TRANSCRIPT RESULTING FROM THE T(14-18) TRANSLOCATION [J].
CLEARY, ML ;
SMITH, SD ;
SKLAR, J .
CELL, 1986, 47 (01) :19-28
[9]   MODULAR BINDING DOMAINS IN SIGNAL-TRANSDUCTION PROTEINS [J].
COHEN, GB ;
REN, RB ;
BALTIMORE, D .
CELL, 1995, 80 (02) :237-248
[10]  
CORTEZ D, 1995, MOL CELL BIOL, V15, P5531