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Over-expression of the Arabidopsis DRE/CRT-binding transcription factor DREB2C enhances thermotolerance

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dc.contributor.authorLim, Chan Ju-
dc.contributor.authorHwang, Jung Eun-
dc.contributor.authorChen, Huan-
dc.contributor.authorHong, Joon Ki-
dc.contributor.authorYang, Kyung Ae-
dc.contributor.authorChoi, Man Soo-
dc.contributor.authorLee, Kyun Oh-
dc.contributor.authorChung, Woo Sik-
dc.contributor.authorLee, Sang Yeol-
dc.contributor.authorLim, Chae Oh-
dc.date.accessioned2022-12-27T06:52:13Z-
dc.date.available2022-12-27T06:52:13Z-
dc.date.issued2007-10-19-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/28265-
dc.description.abstractThe dehydration responsive element binding protein 2 (DREB2) subgroup belongs to the plant-specific APETALA2/ethylene-responsive element binding factor (AP2/ERF) family of transcription factors. We have characterized cDNA encoding Arabidopsis thaliana DREB2C, which is induced by mild heat stress. Both an electrophoretic mobility shift assay (ENISA) and a yeast one-hybrid assay revealed that DREB2C(145-128) was able to form a complex with the dehydration responsive element/Grepeat (DRE/CRT; A/GCCGAC) motif. A trans-activating ability test in yeast demonstrated that DREB2C could effectively function as a trans-activator. ConstitUtive expression of DREB2C under the control of the cauliflower mosaic virus (CaMV) 35S promoter led to enhanced thermotolerance in transgenic lines of Arabidopsis. Microarray and RT-PCR analyses of transgenic plants revealed that DREB2C regulates expression of several heat stress-inducible genes that contain DRE/CRT elements in their promoters. From these data, we deduced that DREB2C is a regulator of heat stress tolerance in Arabidopsis. (c) 2007 Elsevier Inc. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleOver-expression of the Arabidopsis DRE/CRT-binding transcription factor DREB2C enhances thermotolerance-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2007.08.007-
dc.identifier.wosid000249464800036-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.362, no.2, pp 431 - 436-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume362-
dc.citation.number2-
dc.citation.startPage431-
dc.citation.endPage436-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusRESPONSIVE GENE-EXPRESSION-
dc.subject.keywordPlusHEAT-SHOCK PROTEINS-
dc.subject.keywordPlusFUNCTIONAL-ANALYSIS-
dc.subject.keywordPlusCELL-CULTURES-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusDROUGHT-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusTEMPERATURE-
dc.subject.keywordPlusMICROARRAY-
dc.subject.keywordPlusCOLD-
dc.subject.keywordAuthorgene expression-
dc.subject.keywordAuthorheat stress-
dc.subject.keywordAuthormicroarray analysis-
dc.subject.keywordAuthortransgenic plant-
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