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DHS-21, a dicarbonyl/L-xylulose reductase (DCXR) ortholog, regulates longevity and reproduction in Caenorhabditis elegans

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dc.contributor.authorSon, Le Tho-
dc.contributor.authorKo, Kyung-Min-
dc.contributor.authorCho, Jeong Hoon-
dc.contributor.authorSingaravelu, Gunasekaran-
dc.contributor.authorChatterjee, Indrani-
dc.contributor.authorChoi, Tae-Woo-
dc.contributor.authorSong, Hyun-Ok-
dc.contributor.authorYu, Jae-Ran-
dc.contributor.authorPark, Byung-Jae-
dc.contributor.authorLee, Sun-Kyung-
dc.contributor.authorAhnn, Joohong-
dc.date.accessioned2022-07-16T20:50:17Z-
dc.date.available2022-07-16T20:50:17Z-
dc.date.created2021-05-12-
dc.date.issued2011-05-
dc.identifier.issn0014-5793-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/168568-
dc.description.abstractDicarbonyl/L-xylulose reductase (DCXR) converts L-xylulose into xylitol, and reduces various a-dicarbonyl compounds, thus performing a dual role in carbohydrate metabolism and detoxification. In this study, we identified DHS-21 as the only DCXR ortholog in Caenorhabditis elegans. The dhs-21 gene is expressed in various tissues including the intestine, gonadal sheath cells, uterine seam (utse) cells, the spermathecal-uterus (sp-ut) valve and on the plasma membrane of spermatids. Recombinant DHS-21 was shown to convert L-xylulose to xylitol using NADPH as a cofactor. Dhs-21 null mutants of C. elegans show defects in longevity, reproduction and egg-laying. Knock-down of daf-16 and elt-2 transcription factors affected dhs-21 expression. These results suggest that DHS-21 is a bona fide DCXR of C. elegans, essential for normal life span and reproduction.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.titleDHS-21, a dicarbonyl/L-xylulose reductase (DCXR) ortholog, regulates longevity and reproduction in Caenorhabditis elegans-
dc.typeArticle-
dc.contributor.affiliatedAuthorAhnn, Joohong-
dc.identifier.doi10.1016/j.febslet.2011.03.062-
dc.identifier.scopusid2-s2.0-79955597237-
dc.identifier.wosid000290248300010-
dc.identifier.bibliographicCitationFEBS LETTERS, v.585, no.9, pp.1310 - 1316-
dc.relation.isPartOfFEBS LETTERS-
dc.citation.titleFEBS LETTERS-
dc.citation.volume585-
dc.citation.number9-
dc.citation.startPage1310-
dc.citation.endPage1316-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusC-ELEGANS-
dc.subject.keywordPlusLIFE-SPAN-
dc.subject.keywordPlusOVULATION-
dc.subject.keywordPlusLOCALIZATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusKIDNEY-
dc.subject.keywordPlusYEAST-
dc.subject.keywordAuthordhs-21-
dc.subject.keywordAuthorL-Xylulose reductase-
dc.subject.keywordAuthorLongevity-
dc.subject.keywordAuthorEgg-laying-
dc.subject.keywordAuthorGene expression-
dc.identifier.urlhttps://febs.onlinelibrary.wiley.com/doi/full/10.1016/j.febslet.2011.03.062-
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