Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2004-5-25
pubmed:abstractText
We describe the involvement of poly(ADP-ribose)polymerase 1 and 2 (PARP-1 and -2) and poly(ADP-ribose)glycohydrolase (PARG) in the response of rat germinal cells to the action of the NO donors, 3-morpholino-sydnonimine (SIN-1) and spermine nonoate (SNO). Primary spermatocytes and round spermatids showed a differential sensitivity to DNA damage induced by acute exposure to SIN-1 and SNO. Spermatocytes were able to repair DNA damage caused by the release of NO from SNO but neither spermatocytes nor spermatids could recover from the release of NO and O2*- from SIN-1. Addition of the PARPs inhibitor, 3-aminobenzamide, and the PARG inhibitor, gallotannin (GT), to germ cell cultures impaired DNA repair significantly. Consistent with the DNA repair seen in primary spermatocytes, both SIN-1 and SNO induced PARPs activation in these cells. In the case of SIN-1, there was an immediate but transient response while SNO induced a delayed but more sustained increase in PARPs activity. Chronic exposure of spermatocytes to SIN-1 and SNO, however, committed the cells to apoptosis, which coincided with proteolysis of PARP-1. The data indicate a dual role for PARPs and PARG in germinal cells as key proteins in processes that sense and repair DNA damage as well as in the commitment to apoptosis following prolonged oxidative stress.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/3-aminobenzamide, http://linkedlifedata.com/resource/pubmed/chemical/3-morpholino-sydnonimine, http://linkedlifedata.com/resource/pubmed/chemical/Adprt protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Benzamides, http://linkedlifedata.com/resource/pubmed/chemical/Glycoside Hydrolases, http://linkedlifedata.com/resource/pubmed/chemical/Hydrolyzable Tannins, http://linkedlifedata.com/resource/pubmed/chemical/Molsidomine, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Donors, http://linkedlifedata.com/resource/pubmed/chemical/Nitrogen Oxides, http://linkedlifedata.com/resource/pubmed/chemical/Poly(ADP-ribose) Polymerases, http://linkedlifedata.com/resource/pubmed/chemical/Spermine, http://linkedlifedata.com/resource/pubmed/chemical/poly ADP-ribose glycohydrolase, http://linkedlifedata.com/resource/pubmed/chemical/spermine nitric oxide complex
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0006-3002
pubmed:author
pubmed:issnType
Print
pubmed:day
28
pubmed:volume
1692
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
35-44
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15158362-Animals, pubmed-meshheading:15158362-Apoptosis, pubmed-meshheading:15158362-Benzamides, pubmed-meshheading:15158362-Blotting, Western, pubmed-meshheading:15158362-DNA Damage, pubmed-meshheading:15158362-DNA Repair, pubmed-meshheading:15158362-Enzyme Activation, pubmed-meshheading:15158362-Germ Cells, pubmed-meshheading:15158362-Glycoside Hydrolases, pubmed-meshheading:15158362-Hydrolyzable Tannins, pubmed-meshheading:15158362-In Situ Nick-End Labeling, pubmed-meshheading:15158362-Male, pubmed-meshheading:15158362-Molsidomine, pubmed-meshheading:15158362-Nitric Oxide Donors, pubmed-meshheading:15158362-Nitrogen Oxides, pubmed-meshheading:15158362-Oxidative Stress, pubmed-meshheading:15158362-Poly(ADP-ribose) Polymerases, pubmed-meshheading:15158362-Rats, pubmed-meshheading:15158362-Spermatids, pubmed-meshheading:15158362-Spermatocytes, pubmed-meshheading:15158362-Spermine, pubmed-meshheading:15158362-Time Factors
pubmed:year
2004
pubmed:articleTitle
Dual role for poly(ADP-ribose)polymerase-1 and -2 and poly(ADP-ribose)glycohydrolase as DNA-repair and pro-apoptotic factors in rat germinal cells exposed to nitric oxide donors.
pubmed:affiliation
Department of Biological Chemistry, University Federico II of Naples, Via Mezzocannone 16, 80134-Naples, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't