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在拟南芥根表皮细胞命运特化过程中,狼人MYB蛋白直接调控CAPRICE转录。

The WEREWOLF MYB protein directly regulates CAPRICE transcription during cell fate specification in the Arabidopsis root epidermis.

作者信息

Ryu Kook Hui, Kang Yeon Hee, Park Young-hwan, Hwang Ildoo, Schiefelbein John, Lee Myeong Min

机构信息

Department of Biology, Yonsei University, Sinchon 134, Seoul 120-749, Korea.

出版信息

Development. 2005 Nov;132(21):4765-75. doi: 10.1242/dev.02055. Epub 2005 Oct 5.

DOI:10.1242/dev.02055
PMID:16207757
Abstract

The Arabidopsis root epidermis is composed of two types of cells, hair cells and non-hair cells, and their fate is determined in a position-dependent manner. WEREWOLF (WER), a R2R3 MYB protein, has been shown genetically to function as a master regulator to control both of the epidermal cell fates. To directly test the proposed role of WER in this system, we examined its subcellular localization and defined its transcriptional activation properties. We show that a WER-GFP fusion protein is functional and accumulates in the nucleus of the N-position cells in the Arabidopsis root epidermis, as expected for a transcriptional regulator. We also find that a modified WER protein with a strong activation domain (WER-VP16) promotes the formation of both epidermal cell types, supporting the view that WER specifies both cell fates. In addition, we used the glucocorticoid receptor (GR) inducible system to show that CPC transcription is regulated directly by WER. Using EMSA, we found two WER-binding sites (WBSs; WBSI and WBSII) in the CPC promoter. WER-WBSI binding was confirmed in vivo using the yeast one-hybrid assay. Binding between the WER protein and both WBSs (WBSI and WBSII), and the importance of the two WBSs in CPC promoter activity were confirmed in Arabidopsis. These results provide experimental support for the proposed role of WER as an activator of gene transcription during the specification of both epidermal cell fates.

摘要

拟南芥根表皮由两种类型的细胞组成,即毛细胞和非毛细胞,它们的命运是以位置依赖的方式决定的。WEREWOLF(WER)是一种R2R3 MYB蛋白,遗传学研究表明它作为主要调节因子控制两种表皮细胞的命运。为了直接测试WER在该系统中的假定作用,我们检测了它的亚细胞定位并确定了其转录激活特性。我们发现,WER-GFP融合蛋白具有功能,并如转录调节因子所预期的那样,在拟南芥根表皮的N位置细胞的细胞核中积累。我们还发现,带有强激活结构域的修饰WER蛋白(WER-VP16)促进了两种表皮细胞类型的形成,支持了WER决定两种细胞命运的观点。此外,我们使用糖皮质激素受体(GR)诱导系统表明,CPC转录直接受WER调控。通过电泳迁移率变动分析(EMSA),我们在CPC启动子中发现了两个WER结合位点(WBSs;WBSI和WBSII)。使用酵母单杂交试验在体内证实了WER与WBSI的结合。在拟南芥中证实了WER蛋白与两个WBSs(WBSI和WBSII)之间的结合,以及两个WBSs在CPC启动子活性中的重要性。这些结果为WER在两种表皮细胞命运特化过程中作为基因转录激活因子的假定作用提供了实验支持。

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