MOLECULAR-GENETICS OF CELL-DEATH IN THE NEMATODE CAENORHABDITIS-ELEGANS

被引:62
|
作者
DRISCOLL, M
机构
[1] Department of Molecular Biology and Biochemistry, Rutgers University, Center for Advanced Biotechnology and Medicine, Piscataway, New Jersey
来源
JOURNAL OF NEUROBIOLOGY | 1992年 / 23卷 / 09期
关键词
PROGRAMMED CELL DEATH; VACUOLIZATION; GENETIC PATHWAY; NEURODEGENERATION; DOMINANT DISORDER; NECROSIS; APOPTOSIS;
D O I
10.1002/neu.480230919
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In C. elegans, cell death can be readily studied at the cellular, genetic, and molecular levels. Two types of death have been characterized in this nematode: (1) programmed cell death, which occurs as a normal component in development; and (2) pathological cell death, which occurs aberrantly as a consequence of mutation. Analysis of mutations that disrupt programmed cell death in various ways has defined a genetic pathway for programmed cell death which includes genes that perform such functions as the determination of which cells die, the execution of cell death, the engulfment of cell corpses, and the digestion of DNA from dead cells. Molecular analysis is providing insightinto the nature of the molecules that function in these aspects of programmed cell death. Characterization of some genes that mutate to induce abnormal cell death has defined a novel gene family called degenerins that encode putative membrane proteins. Dominant alleles of at least two degenerin genes, mec-4 and deg-1, can cause cellular swelling and late onset neurodegeneration of specific groups of cells.
引用
收藏
页码:1327 / 1351
页数:25
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