Luman is capable of binding and activating transcription from the unfolded protein response element

被引:82
作者
DenBoer, LM [1 ]
Hardy-Smith, PW [1 ]
Hogan, MR [1 ]
Cockram, GP [1 ]
Audas, TE [1 ]
Lu, R [1 ]
机构
[1] Univ Guelph, Dept Mol & Cellular Biol, Guelph, ON N1G 2W1, Canada
基金
加拿大健康研究院;
关键词
unfolded protein response; endoplasmic reticulum stress response; luman/LZIP/CREB3; ER degradation enhancing a-mannosidase-like protein; ER-associated degradation;
D O I
10.1016/j.bbrc.2005.03.141
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
Luman (or LZIP, CREB3) is a transcription factor with an endoplasmic reticulum (ER)-transmembrane domain. Due to its structural similarities with ATF6, it is thought that Luman might also be involved in cellular stress responses. Here we report that Luman can bind and activate transcription from the consensus unfolded protein response element (UPRE). Mutations that disrupted the binding of Luman to the UPREs impaired its ability to activate transcription from these sites. Overexpression of Luman stimulated transcription of EDEM, a downstream effector of the mammalian unfolded protein response involved in ER-associated degradation (ERAD). Unlike ATF6, however, Luman was not activated by proteolytic cleavage in response to endoplasmic reticulum stressors such as tunicamycin and thapsigargin. These results suggest that the activation of ERAD by Luman is likely through a pathway different from the common ER stress response, and that additional factor(s) are required for the activation of this Luman-mediated pathway. 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:113 / 119
页数:7
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