DAD-1, AN ENDOGENOUS PROGRAMMED CELL-DEATH SUPPRESSOR IN CAENORHABDITIS-ELEGANS AND VERTEBRATES

被引:105
作者
SUGIMOTO, A
HOZAK, RR
NAKASHIMA, T
NISHIMOTO, T
ROTHMAN, JH
机构
[1] UNIV WISCONSIN,DEPT BIOCHEM,MADISON,WI 53706
[2] KYUSHU UNIV,GRAD SCH MED SCI,DEPT OTORHINOLARYNGOL,HIGASHI KU,FUKUOKA 812,JAPAN
[3] KYUSHU UNIV,GRAD SCH MED SCI,DEPT MOLEC SCI,HIGASHI KU,FUKUOKA 812,JAPAN
关键词
APOPTOSIS; CAENORHABDITIS ELEGANS; DAD-1; PLANTS; PROGRAMMED CELL DEATH;
D O I
10.1002/j.1460-2075.1995.tb00122.x
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
Programmed cell death (apoptosis) is a normally occurring process used to eliminate unnecessary or potentially harmful cells in multicellular organisms. Recent studies demonstrate that the molecular control of this process is conserved phylogenetically in animals. The dad-1 gene, which encodes a novel 113 amino acid protein, was originally identified in a mutant hamster cell line (tsBN7) that undergoes apoptosis at restrictive temperature. We have identified a dad-1 homologue in Caenorhabditis elegans (Ce-dad-1) whose predicted product is >60% identical to vertebrate DAD-1. A search of the sequence databases indicated that DAD-1-like proteins are also expressed in two plant species. Expression of either human dad-1 or Ce-dad-1 under control of a C.elegans heat-shock-inducible promoter resulted in a reduction in the number of programmed cell death corpses visible in C.elegans embryos. Extra surviving cells were present in these animals, indicating that both the human and C.elegans dad-1 genes can suppress developmentally programmed cell death. Ce-dad-1 was found to rescue mutant tsBN7 hamster cells from apoptotic death as efficiently as the vertebrate genes. These results suggest that dad-1, which is necessary for cell survival in a mammalian cell line, is sufficient to suppress some programmed cell death in C.elegans.
引用
收藏
页码:4434 / 4441
页数:8
相关论文
共 56 条
[1]  
BARSTEAD RJ, 1989, J BIOL CHEM, V264, P10177
[2]   AN APOPTOSIS-INHIBITING GENE FROM A NUCLEAR POLYHEDROSIS-VIRUS ENCODING A POLYPEPTIDE WITH CYS/HIS SEQUENCE MOTIF [J].
BIRNBAUM, MJ ;
CLEM, RJ ;
MILLER, LK .
JOURNAL OF VIROLOGY, 1994, 68 (04) :2521-2528
[3]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608
[4]  
BRENNER S, 1974, GENETICS, V77, P71
[5]  
CASCIOLAROSEN LA, 1994, J BIOL CHEM, V269, P30757
[6]   TRACING TRACHEARY ELEMENT DEVELOPMENT [J].
CHASAN, R .
PLANT CELL, 1994, 6 (07) :917-919
[7]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752
[8]   PREVENTION OF APOPTOSIS BY A BACULOVIRUS GENE DURING INFECTION OF INSECT CELLS [J].
CLEM, RJ ;
FECHHEIMER, M ;
MILLER, LK .
SCIENCE, 1991, 254 (5036) :1388-1390
[9]   CONTROL OF PROGRAMMED CELL-DEATH BY THE BACULOVIRUS GENES P35 AND IAP [J].
CLEM, RJ ;
MILLER, LK .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (08) :5212-5222
[10]   INSERTION OF PART OF AN INTRON INTO THE 5' UNTRANSLATED REGION OF A CAENORHABDITIS-ELEGANS GENE CONVERTS IT INTO A TRANS-SPLICED GENE [J].
CONRAD, R ;
THOMAS, J ;
SPIETH, J ;
BLUMENTHAL, T .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (04) :1921-1926