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Molecular Structure of the GARP Family of Plant Myb-Related DNA Binding Motifs of the Arabidopsis Response Regulators

机译:拟南芥响应调节因子的植物Myb相关DNA结合基序的GARP家族的分子结构。

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摘要

The B motif is a signature of type-B response regulators (ARRs) involved in His-to-Asp phosphorelay signal transduction systems in Arabidopsis. Homologous motifs occur widely in the GARP family of plant transcription factors. To gain general insight into the structure and function of B motifs (or GARP motifs), we characterized the B motif derived from a representative ARR, ARR10, which led to a number of intriguing findings. First, the B motif of ARR10 (named ARR10-B and extending from Thr-179 to Ser-242) possesses a nuclear localization signal, as indicated by the intracellular localization of a green fluorescent protein–ARR10-B fusion protein in onion epidermal cells. Second, the purified ARR10-B molecule binds specifically in vitro to DNA with the core sequence AGATT. This was demonstrated by several in vitro approaches, including PCR-assisted DNA binding site selection, gel retardation assays, and surface plasmon resonance analysis. Finally, the three-dimensional structure of ARR10-B in solution was determined by NMR spectroscopy, showing that it contains a helix-turn-helix structure. Furthermore, the mode of interaction between ARR10-B and the target DNA was assessed extensively by NMR spectroscopy. Together, these results lead us to propose that the mechanism of DNA recognition by ARR10-B is essentially the same as that of homeodomains. We conclude that the B motif is a multifunctional domain responsible for both nuclear localization and DNA binding and suggest that these insights could be applicable generally to the large GARP family of plant transcription factors.
机译:B基序是参与拟南芥中His-Asp磷酸化信号转导系统的B型应答调节器(ARR)的标志。同源基序广泛存在于植物转录因子的GARP家族中。为了获得对B主题(或GARP主题)的结构和功能的一般了解,我们对源自代表性ARR ARR10的B主题进行了表征,从而得出了许多有趣的发现。首先,ARR10的B基序(命名为ARR10-B,从Thr-179延伸到Ser-242)具有核定位信号,绿色荧光蛋白–ARR10-B融合蛋白在洋葱表皮细胞中的胞内定位表明。其次,纯化的ARR10-B分子在体外与具有核心序列AGATT的DNA特异性结合。这已通过几种体外方法得到证实,包括PCR辅助DNA结合位点选择,凝胶阻滞测定和表面等离振子共振分析。最后,通过NMR光谱法确定溶液中ARR10-B的三维结构,表明其含有螺旋-转-螺旋结构。此外,通过NMR光谱对ARR10-B与目标DNA之间的相互作用方式进行了广泛评估。在一起,这些结果使我们提出ARR10-B的DNA识别机制与同源域的机制基本相同。我们得出的结论是B母题是负责核定位和DNA结合的多功能域,并建议这些见解可普遍适用于植物转录因子的大GARP家族。

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