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Characterization of the Aspergillus parasiticus major nitrogen regulatory gene, areA

机译:寄生曲霉主要氮调控基因areA的鉴定

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摘要

The major nitrogen regulatory gene, areA, was cloned from Aspergillus parasiticus. It encoded a polypeptide of 864 amino acids which contained a nuclear localization signal (NLS), a highly acidic region from positions 497 to 542, a Cys-X_2-Cys-X_(17)-Cys-X_2-Cys DNA-binding motif and a conserved carboxy-terminus. Electrophoretic mobility shift assays suggested that the A. parasiticus AREA DNA-binding domain fusion protein bound cooperatively to single GATA elements in the A. parasiticus niaD-niiA intergenic region. AREA also bound to the aflR-aflJ intergenic region of the aflatoxin biosynthesis gene cluster. Regions of areA were fused to a yeast GAL4 DNA-binding domain coding region to localize putative transcription activation domain(s) of AREA based on activation of the GAL1(p)::lacZ reporter gene expression. The portion between NLS and the acidic domain demonstrated 16-20-fold higher activation activities than other portions of AREA, which suggests that the transcription domain is located in this region.
机译:主要的氮调节基因areA是从寄生曲霉中克隆的。它编码了864个氨基酸的多肽,其中包含一个核定位信号(NLS),一个从497-542位的高酸性区域,一个Cys-X_2-Cys-X_(17)-Cys-X_2-Cys DNA结合基序和保守的羧基末端。电泳迁移率迁移分析表明,副寄生曲霉AREA DNA结合域融合蛋白与副寄生曲霉niaD-niiA基因间区域中的单个GATA元件协同结合。 AREA也与黄曲霉毒素生物合成基因簇的aflR-aflJ基因间区域结合。 areA区域与酵母GAL4 DNA结合域编码区融合,从而基于GAL1(p):: lacZ报告基因表达的激活来定位AREA的假定转录激活域。 NLS和酸性域之间的部分显示出比AREA其他部分高16-20倍的激活活性,这表明转录域位于该区域。

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