XBP1 activates the transcription of its target genes via an ACGT core sequence under ER stress

被引:61
作者
Kanemoto, S
Kondo, S
Ogata, M
Murakami, T
Urano, F
Imaizumi, K
机构
[1] Miyazaki Univ, Fac Med, Dept Anat, Div Mol & Cellular Biol, Kiyotake, Miyazaki 8891692, Japan
[2] NAIST, Div Struct Cellular Biol, Nara 6300101, Japan
[3] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
关键词
XBP1; UPR; ER stress; ACGT core; transcription; IRE1; cis-element;
D O I
10.1016/j.bbrc.2005.04.039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1146 / 1153
页数:8
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