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dc.contributor.authorKanemoto, Soshi
dc.contributor.authorKondo, Shinichi
dc.contributor.authorOgata, Maiko
dc.contributor.authorMurakami, Tomohiko
dc.contributor.authorUrano, Fumihiko
dc.contributor.authorImaizumi, Kazunori
dc.date2022-08-11T08:10:15.000
dc.date.accessioned2022-08-23T17:01:02Z
dc.date.available2022-08-23T17:01:02Z
dc.date.issued2005-05-11
dc.date.submitted2011-04-19
dc.identifier.citationBiochem Biophys Res Commun. 2005 Jun 17;331(4):1146-53. <a href="http://dx.doi.org/10.1016/j.bbrc.2005.04.039">Link to article on publisher's site</a>
dc.identifier.issn0006-291X (Linking)
dc.identifier.doi10.1016/j.bbrc.2005.04.039
dc.identifier.pmid15882996
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43919
dc.description.abstractIn mammals, the transmembrane protein kinase/endoribonuclease IRE1 is activated by endoplasmic reticulum stress and subsequently processes XBP1 mRNA to generate an active form of XBP1 protein. The spliced form of XBP1 protein acts as a transcription factor and induces the expression of ER-resident molecular chaperones. However, the mechanism for how XBP1 promotes the transcription of its target genes as well as the cis-acting elements for XBP1 during ER stress has been unclear. Recently, it was demonstrated that the expression of MDG1/ERdj4, a member of the DnaJ family, is regulated by the IRE1-XBP1 pathway. In the present report, we investigated the regulatory mechanisms of MDG1/ERdj4 gene expression by XBP1. We identified a cis-acting element in the MDG1/ERdj4 promoter region, to which XBP1 specifically binds in response to ER stress. Our results reveal a target sequence for the IRE1-XBP1 pathway under ER stress conditions.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=15882996&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.bbrc.2005.04.039
dc.subjectBase Sequence
dc.subjectDNA
dc.subjectDNA-Binding Proteins
dc.subjectEndoplasmic Reticulum
dc.subjectHela Cells
dc.subjectHumans
dc.subjectMolecular Sequence Data
dc.subjectNuclear Proteins
dc.subjectPromoter Regions, Genetic
dc.subjectTranscription Factors
dc.subjectTranscription, Genetic
dc.subjectGenetics and Genomics
dc.titleXBP1 activates the transcription of its target genes via an ACGT core sequence under ER stress
dc.typeJournal Article
dc.source.journaltitleBiochemical and biophysical research communications
dc.source.volume331
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pgfe_pp/130
dc.identifier.contextkey1946785
html.description.abstract<p>In mammals, the transmembrane protein kinase/endoribonuclease IRE1 is activated by endoplasmic reticulum stress and subsequently processes XBP1 mRNA to generate an active form of XBP1 protein. The spliced form of XBP1 protein acts as a transcription factor and induces the expression of ER-resident molecular chaperones. However, the mechanism for how XBP1 promotes the transcription of its target genes as well as the cis-acting elements for XBP1 during ER stress has been unclear. Recently, it was demonstrated that the expression of MDG1/ERdj4, a member of the DnaJ family, is regulated by the IRE1-XBP1 pathway. In the present report, we investigated the regulatory mechanisms of MDG1/ERdj4 gene expression by XBP1. We identified a cis-acting element in the MDG1/ERdj4 promoter region, to which XBP1 specifically binds in response to ER stress. Our results reveal a target sequence for the IRE1-XBP1 pathway under ER stress conditions.</p>
dc.identifier.submissionpathpgfe_pp/130
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentProgram in Gene Function and Expression
dc.source.pages1146-53


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