Mitochondrial endonuclease G is important for apoptosis in C. elegans
- PMID: 11452313
- DOI: 10.1038/35083608
Mitochondrial endonuclease G is important for apoptosis in C. elegans
Abstract
Programmed cell death (apoptosis) is a tightly regulated process of cell disassembly in which dying cells and their nuclei shrink and fragment and the chromosomal DNA is degraded into internucleosomal repeats. Here we report the characterization of the cps-6 gene, which appears to function downstream of, or in parallel to, the cell-death protease CED-3 of Caenorhabditis elegans in the DNA degradation process during apoptosis. cps-6 encodes a homologue of human mitochondrial endonuclease G, and its protein product similarly localizes to mitochondria in C. elegans. Reduction of cps-6 activity caused by a genetic mutation or RNA-mediated interference (RNAi) affects normal DNA degradation, as revealed by increased staining in a TUNEL assay, and results in delayed appearance of cell corpses during development in C. elegans. This observation provides in vivo evidence that the DNA degradation process is important for proper progression of apoptosis. CPS-6 is the first mitochondrial protein identified to be involved in programmed cell death in C. elegans, underscoring the conserved and important role of mitochondria in the execution of apoptosis.
Comment in
-
Apoptosis. DNA destroyers.Nature. 2001 Jul 5;412(6842):27, 29. doi: 10.1038/35083663. Nature. 2001. PMID: 11452284 No abstract available.
Similar articles
-
Mechanisms of AIF-mediated apoptotic DNA degradation in Caenorhabditis elegans.Science. 2002 Nov 22;298(5598):1587-92. doi: 10.1126/science.1076194. Science. 2002. PMID: 12446902
-
Inhibition of the Caenorhabditis elegans cell-death protease CED-3 by a CED-3 cleavage site in baculovirus p35 protein.Nature. 1995 Sep 21;377(6546):248-51. doi: 10.1038/377248a0. Nature. 1995. PMID: 7675111
-
DRP-1-mediated mitochondrial fragmentation during EGL-1-induced cell death in C. elegans.Nature. 2005 Feb 17;433(7027):754-60. doi: 10.1038/nature03316. Nature. 2005. PMID: 15716954
-
ICE/CED3-like proteases as therapeutic targets for the control of inappropriate apoptosis.Nat Biotechnol. 1996 Mar;14(3):297-301. doi: 10.1038/nbt0396-297. Nat Biotechnol. 1996. PMID: 9630889 Review.
-
The ins and outs of programmed cell death during C. elegans development.Philos Trans R Soc Lond B Biol Sci. 1994 Aug 30;345(1313):243-6. doi: 10.1098/rstb.1994.0100. Philos Trans R Soc Lond B Biol Sci. 1994. PMID: 7846120 Review.
Cited by
-
The roles and acting mechanism of Caenorhabditis elegans DNase II genes in apoptotic dna degradation and development.PLoS One. 2009 Oct 7;4(10):e7348. doi: 10.1371/journal.pone.0007348. PLoS One. 2009. PMID: 19809494 Free PMC article.
-
Leishmania infantum EndoG is an endo/exo-nuclease essential for parasite survival.PLoS One. 2014 Feb 26;9(2):e89526. doi: 10.1371/journal.pone.0089526. eCollection 2014. PLoS One. 2014. PMID: 24651293 Free PMC article.
-
Cellular and nuclear degradation during apoptosis.Curr Opin Cell Biol. 2009 Dec;21(6):900-12. doi: 10.1016/j.ceb.2009.08.008. Epub 2009 Sep 24. Curr Opin Cell Biol. 2009. PMID: 19781927 Free PMC article. Review.
-
Evidence that CED-9/Bcl2 and CED-4/Apaf-1 localization is not consistent with the current model for C. elegans apoptosis induction.Cell Death Differ. 2012 Mar;19(3):406-15. doi: 10.1038/cdd.2011.104. Epub 2011 Sep 2. Cell Death Differ. 2012. PMID: 21886181 Free PMC article.
-
Programmed cell death in Leishmania: biochemical evidence and role in parasite infectivity.Front Cell Infect Microbiol. 2012 Jul 10;2:95. doi: 10.3389/fcimb.2012.00095. eCollection 2012. Front Cell Infect Microbiol. 2012. PMID: 22919685 Free PMC article. Review.
Publication types
MeSH terms
Substances
Associated data
- Actions
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases