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PMID: 9927601 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Genetic control of programmed cell death in the Caenorhabditis elegans hermaphrodite germline.

Development (Cambridge, England) ·Vol. 126 ·No. 5 ·1999-02-00 ·Pages 1011-22

Gumienny TL, Lambie E, Hartwieg E, Horvitz HR, Hengartner MO

Abstract

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.

MeSH Terms
Animals Apoptosis Caenorhabditis elegans/cytology Germ Cells/cytology Homeostasis Sex Differentiation
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Gumienny T L
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11743, USA and Program in Genetics, State University of New York at Stony Brook, Stony Brook, NY 11794, USA.
Lambie E
Hartwieg E
Horvitz H R
Hengartner M O
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1999-02-00
Pages
1011-22
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · GM49785 · United States
NIGMS NIH HHS · GM525420 · United States
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