Browse

Induction of a SSAT isoform in response to hypoxia or iron deficiency and its protective effects on cell death

DC Field Value Language
dc.contributor.authorKim, Kyuheun-
dc.contributor.authorRyu, Ji-Hye-
dc.contributor.authorPark, Jong-Wan-
dc.contributor.authorKim, Myung-Suk-
dc.contributor.authorChun, Yang-Sook-
dc.date.accessioned2010-01-20T02:33:10Z-
dc.date.available2010-01-20T02:33:10Z-
dc.date.issued2006-04-23-
dc.identifier.citationBiochem Biophys Res Commun. 2005 May 27;331(1):78-85.en
dc.identifier.issn0006-291X (Print)-
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=15845361-
dc.identifier.urihttp://hdl.handle.net/10371/39196-
dc.description.abstractSpermidine/spermine N(1)-acetyltransferase (SSAT) is the key enzyme with regard to the maintenance of intracellular polyamine levels. It is an inducible enzyme, which may participate in adaptive responses to environmental stress. However, little is known regarding its responses to oxygen or nutrient deficiencies. Using microarray assays, we discovered that SSAT was enhanced under both oxygen- and iron-deficient conditions. However, RT-PCR revealed that the SSAT mRNA was not induced; rather, an mRNA variant was newly expressed. In this variant, the splicing-in of 110 bases induces early termination, generating a truncated isoform which lacks catalytic motifs. The variant expression occurs in other cancer cells and was irrelevant to both hypoxia-inducible factor 1 and to the redox state. We attempted to determine its role, using stable cell-lines. The expressed isoform was found to promote cell survival under iron-deficient conditions and blocked the cleavage of poly(ADP-ribose) polymerase. This isoform may contribute to the progression of tumors of a more malignant phenotype under poor conditions and may constitute a potential target for anticancer therapy.en
dc.language.isoen-
dc.publisherElsevieren
dc.subjectAcetyltransferases/biosynthesis/genetics/*physiologyen
dc.subjectAlternative Splicingen
dc.subjectAmino Acid Sequenceen
dc.subjectCell Hypoxiaen
dc.subjectCell Line, Tumoren
dc.subjectCell Proliferationen
dc.subjectCell Survivalen
dc.subjectEnzyme Inductionen
dc.subjectHumansen
dc.subjectIron/*physiologyen
dc.subjectIsoenzymes/biosynthesis/genetics/physiologyen
dc.subjectMolecular Sequence Dataen
dc.subjectNeoplasms/*enzymologyen
dc.subjectRNA, Messenger/metabolismen
dc.titleInduction of a SSAT isoform in response to hypoxia or iron deficiency and its protective effects on cell deathen
dc.typeArticleen
dc.contributor.AlternativeAuthor김규헌-
dc.contributor.AlternativeAuthor류지혜-
dc.contributor.AlternativeAuthor박종완-
dc.contributor.AlternativeAuthor김명석-
dc.contributor.AlternativeAuthor전양숙-
dc.identifier.doi10.1016/j.bbrc.2005.03.121-
Appears in Collections:
College of Medicine/School of Medicine (의과대학/대학원)Molecular and Genomic Medicine (분자유전체의학전공)Journal Papers (저널논문_분자유전체의학전공)
Files in This Item:
There are no files associated with this item.
  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse