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对依赖TALE的基因激活的剖析表明,它们以协同方式且在两个方向上诱导转录。

Dissection of TALE-dependent gene activation reveals that they induce transcription cooperatively and in both orientations.

作者信息

Streubel Jana, Baum Heidi, Grau Jan, Stuttmann Johannes, Boch Jens

机构信息

Institute of Plant Genetics, Leibniz Universität Hannover, Hannover, Germany.

Department of Plant Genetics, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Germany.

出版信息

PLoS One. 2017 Mar 16;12(3):e0173580. doi: 10.1371/journal.pone.0173580. eCollection 2017.

Abstract

Plant-pathogenic Xanthomonas bacteria inject transcription activator-like effector proteins (TALEs) into host cells to specifically induce transcription of plant genes and enhance susceptibility. Although the DNA-binding mode is well-understood it is still ambiguous how TALEs initiate transcription and whether additional promoter elements are needed to support this. To systematically dissect prerequisites for transcriptional initiation the activity of one TALE was compared on different synthetic Bs4 promoter fragments. In addition, a large collection of artificial TALEs spanning the OsSWEET14 promoter was compared. We show that the presence of a TALE alone is not sufficient to initiate transcription suggesting the requirement of additional supporting promoter elements. At the OsSWEET14 promoter TALEs can initiate transcription from various positions, in a synergistic manner of multiple TALEs binding in parallel to the promoter, and even by binding in reverse orientation. TALEs are known to shift the transcriptional start site, but our data show that this shift depends on the individual position of a TALE within a promoter context. Our results implicate that TALEs function like classical enhancer-binding proteins and initiate transcription in both orientations which has consequences for in planta target gene prediction and design of artificial activators.

摘要

植物致病黄单胞菌将转录激活样效应蛋白(TALEs)注入宿主细胞,以特异性诱导植物基因转录并增强易感性。尽管DNA结合模式已被充分理解,但TALEs如何启动转录以及是否需要额外的启动子元件来支持这一过程仍不明确。为了系统地剖析转录起始的先决条件,我们比较了一种TALE在不同合成Bs4启动子片段上的活性。此外,还比较了一系列跨越OsSWEET14启动子的人工TALEs。我们发现,仅TALE的存在不足以启动转录,这表明需要额外的支持性启动子元件。在OsSWEET14启动子上,TALEs可以从多个位置启动转录,多个TALEs以协同方式平行结合到启动子上,甚至以反向结合的方式启动转录。已知TALEs会改变转录起始位点,但我们的数据表明,这种改变取决于TALE在启动子背景中的个体位置。我们的结果表明,TALEs的功能类似于经典的增强子结合蛋白,并且可以双向启动转录,这对植物体内靶基因预测和人工激活剂的设计具有重要意义。

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