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利用全面的酵母单杂交筛选鉴定Zat12的新型转录调节因子。

Identification of novel transcriptional regulators of Zat12 using comprehensive yeast one-hybrid screens.

作者信息

Ben Daniel Bat-Hen, Cattan Esther, Wachtel Chaim, Avrahami Dorit, Glick Yair, Malichy Asaf, Gerber Doron, Miller Gad

机构信息

The Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, 5290002, Israel.

The Nanotechnology Institute, The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, 5290002, Israel.

出版信息

Physiol Plant. 2016 Aug;157(4):422-41. doi: 10.1111/ppl.12439. Epub 2016 Apr 14.

Abstract

To appropriately acclimate to environmental stresses, plants have to rapidly activate a specific transcriptional program. Yet, the identity and function of many of the transcriptional regulators that mediate early responses to abiotic stress stimuli is still unknown. In this work we employed the promoter of the multi-stress-responsive zinc-finger protein Zat12 in yeast one-hybrid (Y1H) screens to identify early abiotic stress-responsive transcriptional regulators. Analysis of Zat12 promoter fragments fused to luciferase underlined an approximately 200 bp fragment responsive to NaCl and to reactive oxygen species (ROS). Using these segments and others as baits against Y1H control or stress Arabidopsis prey libraries, we identified 15 potential Zat12 transcriptional regulators. Among the prominent proteins identified were known transcription factors including bZIP29 and ANAC91 as well as unknown function proteins such as a homolog of the human USB1, a U6 small nuclear RNA (snRNA) processing protein, and dormancy/auxin-associated family protein 2 (DRM2). Altered expression of Zat12 during high light stress in the knockout mutants further indicated the involvement of these proteins in the regulation of Zat12. Using a state of the art microfluidic approach we showed that AtUSB1 and DRM2 can specifically bind dsDNA and were able to identify the preferred DNA-binding motif of all four proteins. Overall, the proteins identified in this work provide an important start point for charting the earliest signaling network of Zat12 and of other genes required for acclimation to abiotic stresses.

摘要

为了适当地适应环境胁迫,植物必须迅速激活特定的转录程序。然而,许多介导对非生物胁迫刺激早期反应的转录调节因子的身份和功能仍然未知。在这项工作中,我们在酵母单杂交(Y1H)筛选中使用了多胁迫响应锌指蛋白Zat12的启动子,以鉴定早期非生物胁迫响应转录调节因子。对与荧光素酶融合的Zat12启动子片段的分析强调了一个约200 bp的片段,该片段对NaCl和活性氧(ROS)有反应。使用这些片段和其他片段作为诱饵,针对Y1H对照或胁迫拟南芥猎物文库,我们鉴定了15种潜在的Zat12转录调节因子。鉴定出的突出蛋白质包括已知的转录因子,如bZIP29和ANAC91,以及功能未知的蛋白质,如人类USB1的同源物、一种U6小核RNA(snRNA)加工蛋白和休眠/生长素相关家族蛋白2(DRM2)。敲除突变体在高光胁迫期间Zat12的表达改变进一步表明这些蛋白质参与了Zat12的调节。使用最先进的微流控方法,我们表明AtUSB1和DRM2可以特异性结合双链DNA,并能够鉴定所有四种蛋白质的首选DNA结合基序。总体而言,这项工作中鉴定出的蛋白质为绘制Zat12以及适应非生物胁迫所需的其他基因的最早信号网络提供了重要的起点。

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