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bZIP17 and bZIP60 Regulate the Expression of BiP3 and Other Salt Stress Responsive Genes in an UPR-Independent Manner inArabidopsis thaliana

未折叠蛋白反应 钙连接素 细胞生物学 生物 钙网蛋白 转录因子 内质网 RNA剪接 伴侣(临床) 细胞应激反应 拟南芥 基因 拟南芥 抄写(语言学) 突变体 遗传学 战斗或逃跑反应 核糖核酸 医学 病理 语言学 哲学
作者
Carlos Henríquez-Valencia,Adrián A. Moreno,Omar Sandoval-Ibáñez,Irina Mitina,Francisca Blanco‐Herrera,Nicolás Cifuentes‐Esquivel,Ariel Orellana
出处
期刊:Journal of Cellular Biochemistry [Wiley]
卷期号:116 (8): 1638-1645 被引量:56
标识
DOI:10.1002/jcb.25121
摘要

Plants can be severely affected by salt stress. Since these are sessile organisms, they have developed different cellular responses to cope with this problem. Recently, it has been described that bZIP17 and bZIP60, two ER-located transcription factors, are involved in the cellular response to salt stress. On the other hand, bZIP60 is also involved in the unfolded protein response (UPR), a signaling pathway that up-regulates the expression of ER-chaperones. Coincidentally, salt stress produces the up-regulation of BiP, one of the main chaperones located in this organelle. Then, it has been proposed that UPR is associated to salt stress. Here, by using insertional mutant plants on bZIP17 and bZIP60, we show that bZIP17 regulate the accumulation of the transcript for the chaperone BiP3 under salt stress conditions, but does not lead to the accumulation of UPR-responding genes such as the chaperones Calnexin, Calreticulin, and PDIL under salt treatments. In contrast, DTT, a known inducer of UPR, leads to the up-regulation of all these chaperones. On the other hand, we found that bZIP60 regulates the expression of some bZIP17 target genes under conditions were splicing of bZIP60 does not occur, suggesting that the spliced and unspliced forms of bZIP60 play different roles in the physiological response of the plant. Our results indicate that the ER-located transcription factors bZIP17 and bZIP60 play a role in salt stress but this response goes through a signaling pathway that is different to that triggered by the unfolded protein response. J. Cell. Biochem. 116: 1638–1645, 2015. © 2015 Wiley Periodicals, Inc.
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