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The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2–His2 zinc finger motif

机译:拟南芥SUPERMAN蛋白能够通过其单个的Cys2-His2锌指基序特异性结合DNA

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摘要

The Arabidopsis SUPERMAN (SUP) gene has been shown to be important in maintaining the boundary between stamens and carpels, and is presumed to act by regulating cell proliferation. In this work, we show that the SUP protein, which contains a single Cys2–His2 zinc finger domain including the QALGGH sequence, highly conserved in the plant zinc finger proteins, binds DNA. Using a series of deletion mutants, it was determined that the minimal domain required for specific DNA binding (residues 15–78) includes the single zinc finger and two basic regions located on either side of this motif. Furthermore, amino acid substitutions in the zinc finger or in the basic regions, including a mutation that knocks out the function of the SUP protein in vivo (glycine 63 to aspartate), have been found to abolish the activity of the SUP DNA-binding domain. These results strongly suggest that the SUP protein functions in vivo by acting as a DNA-binding protein, likely involved in transcriptional regulation. The association of both an N-terminal and a C-terminal basic region with a single Cys2–His2 zinc finger represents a novel DNA-binding motif suggesting that the mechanism of DNA recognition adopted by the SUP protein is different from that described so far in other zinc finger proteins.
机译:拟南芥SUPERMAN(SUP)基因在维持雄蕊和心皮之间的边界方面很重要,并且推测是通过调节细胞增殖来发挥作用的。在这项工作中,我们证明了SUP蛋白与DNA结合,该SUP蛋白包含一个单一的Cys2-His2锌指结构域,其中QALGGH序列在植物锌指蛋白中高度保守。使用一系列缺失突变体,可以确定特异性DNA结合所需的最小结构域(残基15-78)包括单个锌指和位于该基序两侧的两个基本区域。此外,已发现锌指或基本区域中的氨基酸取代(包括敲除体内SUP蛋白功能的突变(甘氨酸63变为天冬氨酸))消除了SUP DNA结合结构域的活性。 。这些结果强烈表明,SUP蛋白通过充当DNA结合蛋白(可能参与转录调控)而在体内发挥作用。 N末端和C末端基本区域与单个Cys2-His2锌指的结合代表了一种新的DNA结合基序,表明SUP蛋白采用的DNA识别机制与迄今为止描述的机制不同。其他锌指蛋白。

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