Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1995-7-13
pubmed:databankReference
pubmed:abstractText
Although the mechanism of mammalian apoptosis has not been elucidated, a protease of the CED-3/ICE family is anticipated to be a component of the death machinery. Several lines of evidence predict that this protease cleaves the death substrate poly(ADP-ribose) polymerase (PARP) to a specific 85 kDa form observed during apoptosis, is inhibitable by the CrmA protein, and is distinct from ICE. We cloned a ced-3/ICE-related gene, designated Yama, that encodes a protein identical to CPP32 beta. Purified Yama was a zymogen that, when activated, cleaved PARP to generate the 85 kDa apoptotic fragment. Cleavage of PARP by Yama was inhibited by CrmA but not by an inactive point mutant of CrmA. Furthermore, CrmA blocked cleavage of PARP in cells undergoing apoptosis. We propose that Yama may represent an effector component of the mammalian cell death pathway and suggest that CrmA blocks apoptosis by inhibiting Yama.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CASP3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Caenorhabditis elegans Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 1, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 3, http://linkedlifedata.com/resource/pubmed/chemical/Caspases, http://linkedlifedata.com/resource/pubmed/chemical/Cysteine Endopeptidases, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Precursors, http://linkedlifedata.com/resource/pubmed/chemical/Helminth Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Poly(ADP-ribose) Polymerases, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Serpins, http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins, http://linkedlifedata.com/resource/pubmed/chemical/ced-3 protein, C elegans, http://linkedlifedata.com/resource/pubmed/chemical/interleukin-1beta-converting...
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0092-8674
pubmed:author
pubmed:issnType
Print
pubmed:day
2
pubmed:volume
81
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
801-9
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:7774019-Apoptosis, pubmed-meshheading:7774019-Caenorhabditis elegans Proteins, pubmed-meshheading:7774019-Caspase 1, pubmed-meshheading:7774019-Caspase 3, pubmed-meshheading:7774019-Caspases, pubmed-meshheading:7774019-Cloning, Molecular, pubmed-meshheading:7774019-Cysteine Endopeptidases, pubmed-meshheading:7774019-DNA, Complementary, pubmed-meshheading:7774019-Enzyme Activation, pubmed-meshheading:7774019-Enzyme Precursors, pubmed-meshheading:7774019-Helminth Proteins, pubmed-meshheading:7774019-Humans, pubmed-meshheading:7774019-Molecular Sequence Data, pubmed-meshheading:7774019-Mutagenesis, pubmed-meshheading:7774019-Mutation, pubmed-meshheading:7774019-Point Mutation, pubmed-meshheading:7774019-Poly(ADP-ribose) Polymerases, pubmed-meshheading:7774019-Precipitin Tests, pubmed-meshheading:7774019-Protein Binding, pubmed-meshheading:7774019-Protein Processing, Post-Translational, pubmed-meshheading:7774019-Recombinant Fusion Proteins, pubmed-meshheading:7774019-Sequence Homology, Amino Acid, pubmed-meshheading:7774019-Serpins, pubmed-meshheading:7774019-Transfection, pubmed-meshheading:7774019-Viral Proteins
pubmed:year
1995
pubmed:articleTitle
Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymerase.
pubmed:affiliation
Department of Pathology, University of Michigan Medical School, Ann Arbor 48109, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't