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Genetic control of programmed cell death in the Caenorhabditis elegans hermaphrodite germline.
Author(s) -
Tina L. Gumienny,
Eric J. Lambie,
Erika Hartwieg,
H. Robert Horvitz,
Michael O. Hengartner
Publication year - 1999
Publication title -
pubmed
Language(s) - English
Resource type - Journals
pISSN - 0950-1991
DOI - 10.1242/dev.126.5.1011
Subject(s) - biology , caenorhabditis elegans , germline , somatic cell , microbiology and biotechnology , programmed cell death , germ cell , apoptosis , genetics , cell fate determination , gene , transcription factor
Development of the nematode Caenorhabditis elegans is highly reproducible and the fate of every somatic cell has been reported. We describe here a previously uncharacterized cell fate in C. elegans: we show that germ cells, which in hermaphrodites can differentiate into sperm and oocytes, also undergo apoptotic cell death. In adult hermaphrodites, over 300 germ cells die, using the same apoptotic execution machinery (ced-3, ced-4 and ced-9) as the previously described 131 somatic cell deaths. However, this machinery is activated by a distinct pathway, as loss of egl-1 function, which inhibits somatic cell death, does not affect germ cell apoptosis. Germ cell death requires ras/MAPK pathway activation and is used to maintain germline homeostasis. We suggest that apoptosis eliminates excess germ cells that acted as nurse cells to provide cytoplasmic components to maturing oocytes.

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