XBP1 activates the transcription of its target genes via an ACGT core sequence under ER stress
| dc.contributor.author | Kanemoto, Soshi | |
| dc.contributor.author | Kondo, Shinichi | |
| dc.contributor.author | Ogata, Maiko | |
| dc.contributor.author | Murakami, Tomohiko | |
| dc.contributor.author | Urano, Fumihiko | |
| dc.contributor.author | Imaizumi, Kazunori | |
| dc.date | 2022-08-11T08:10:15.000 | |
| dc.date.accessioned | 2022-08-23T17:01:02Z | |
| dc.date.available | 2022-08-23T17:01:02Z | |
| dc.date.issued | 2005-05-11 | |
| dc.date.submitted | 2011-04-19 | |
| dc.identifier.citation | Biochem 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.issn | 0006-291X (Linking) | |
| dc.identifier.doi | 10.1016/j.bbrc.2005.04.039 | |
| dc.identifier.pmid | 15882996 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14038/43919 | |
| dc.description.abstract | 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. | |
| dc.language.iso | en_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.url | http://dx.doi.org/10.1016/j.bbrc.2005.04.039 | |
| dc.subject | Base Sequence | |
| dc.subject | DNA | |
| dc.subject | DNA-Binding Proteins | |
| dc.subject | Endoplasmic Reticulum | |
| dc.subject | Hela Cells | |
| dc.subject | Humans | |
| dc.subject | Molecular Sequence Data | |
| dc.subject | Nuclear Proteins | |
| dc.subject | Promoter Regions, Genetic | |
| dc.subject | Transcription Factors | |
| dc.subject | Transcription, Genetic | |
| dc.subject | Genetics and Genomics | |
| dc.title | XBP1 activates the transcription of its target genes via an ACGT core sequence under ER stress | |
| dc.type | Journal Article | |
| dc.source.journaltitle | Biochemical and biophysical research communications | |
| dc.source.volume | 331 | |
| dc.source.issue | 4 | |
| dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/pgfe_pp/130 | |
| dc.identifier.contextkey | 1946785 | |
| 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.submissionpath | pgfe_pp/130 | |
| dc.contributor.department | Program in Molecular Medicine | |
| dc.contributor.department | Program in Gene Function and Expression | |
| dc.source.pages | 1146-53 |