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ER 锚定转录因子 bZIP17 和 bZIP28 调控根伸长。

ER-Anchored Transcription Factors bZIP17 and bZIP28 Regulate Root Elongation.

机构信息

Gene Discovery Research Group, RIKEN Center for Sustainable Resource Science, Tsukuba, Ibaraki 305-0074, Japan.

Laboratory of Plant Molecular Physiology, Graduate School of Agricultural and Life Sciences, University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.

出版信息

Plant Physiol. 2018 Mar;176(3):2221-2230. doi: 10.1104/pp.17.01414. Epub 2018 Jan 24.

Abstract

The unfolded protein response (UPR) is a eukaryotic transcriptional regulatory network that is activated upon the accumulation of malformed proteins in the endoplasmic reticulum (ER). In Arabidopsis (), three bZIP transcription factors modulate the UPR: bZIP17, bZIP28, and bZIP60. Although bZIP28 and bZIP60 have been relatively well studied, the physiological and transcriptional roles of bZIP17 remain largely unknown. Here, we generated a double knockout mutant of bZIP17 and bZIP28 to elucidate the function of bZIP17. The mutant plant exhibited multiple developmental defects, including markedly reduced root elongation and constantly overinduced bZIP60 activity, indicating the essential roles of bZIP17 and bZIP28 in plant development and UPR modulation. Extended analysis of the transcriptomes of three double knockout mutants of , , and revealed that bZIP28 and bZIP60 are the major activators of the canonical induced UPR. By contrast, bZIP17 functions with bZIP28 to mediate the noninducible expression of multiple genes involved in cell growth, particularly to sustain their expression under stress conditions. Our study reveals pivotal roles of bZIP17 in the plant UPR and vegetative development, with functional redundancy to bZIP28.

摘要

未折叠蛋白反应 (UPR) 是一种真核转录调控网络,当内质网 (ER) 中错误折叠的蛋白质积累时,该网络就会被激活。在拟南芥 () 中,有三种 bZIP 转录因子调节 UPR:bZIP17、bZIP28 和 bZIP60。尽管 bZIP28 和 bZIP60 已经得到了相对较好的研究,但 bZIP17 的生理和转录作用在很大程度上仍然未知。在这里,我们生成了 bZIP17 和 bZIP28 的双敲除突变体,以阐明 bZIP17 的功能。该突变体植物表现出多种发育缺陷,包括明显的根伸长减少和持续过度诱导的 bZIP60 活性,这表明 bZIP17 和 bZIP28 在植物发育和 UPR 调节中起着至关重要的作用。对三个双敲除突变体(、和 )的转录组的扩展分析表明,bZIP28 和 bZIP60 是经典诱导 UPR 的主要激活剂。相比之下,bZIP17 与 bZIP28 一起发挥作用,介导涉及细胞生长的多个基因的非诱导表达,特别是在胁迫条件下维持其表达。我们的研究揭示了 bZIP17 在植物 UPR 和营养生长发育中的关键作用,与 bZIP28 具有功能冗余性。

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