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首页> 外文期刊>Molecular Microbiology >Sequence, exon-intron organization, transcription and mutational analysis of prnA, the gene encoding the transcriptional activator of the prn gene cluster in Aspergillus nidulans (published erratum appears in Mol Microbiol 1999 Feb;31(4):1283)
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Sequence, exon-intron organization, transcription and mutational analysis of prnA, the gene encoding the transcriptional activator of the prn gene cluster in Aspergillus nidulans (published erratum appears in Mol Microbiol 1999 Feb;31(4):1283)

机译:prnA的序列,外显子-内含子组织,转录和突变分析,该基因编码构巢曲霉中prn基因簇的转录激活因子(发表的勘误出现在Mol Microbiol 1999年2月; 31(4):1283中)

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摘要

The prnA gene codes for a transcriptional activator that mediates proline induction of four other genes involved in proline utilization as a nitrogen and/or carbon source in Aspergillus nidulans. In this paper, we present the genomic and cDNA sequence and the transcript map of prnA. The PrnA protein belongs to the Zn binuclear cluster family of transcriptional activators. The gene shows a striking intron-exon organization, with the putative nuclear localization sequence and the Zn cluster domain in discrete exons. Although the protein sequence presents some interesting similarities with the isofunctional protein of Saccharomyces cerevisiae Put3p, a higher degree of similarity is found with a functionally unrelated protein Thi1 of Schizosaccharomyces pombe. A number of mutations mapping in the prnA gene were sequenced. This comprises a deletion that results in an almost complete loss of the prnA-specific mRNA, a mutation in the putative nuclear localization signal, a proline to leucine mutation in the second loop of the zinc cluster and a cold-sensitive mutation in the so-called 'central region'. Other complete or partial loss of function mutations map in regions of unknown function. We establish that the transcription of the gene is neither self-regulated nor significantly affected by carbon and/or nitrogen metabolite repression.
机译:prnA基因编码一个转录激活因子,可介导脯氨酸诱导构巢曲霉中作为氮和/或碳源的四个其他脯氨酸利用基因。在本文中,我们介绍了prnA的基因组和cDNA序列以及转录本图谱。 PrnA蛋白属于转录激活因子Zn双核簇家族。该基因显示了一个惊人的内含子-外显子组织,假定的核定位序列和Zn簇结构域位于离散的外显子中。尽管该蛋白序列与酿酒酵母Put3p的同功能蛋白表现出一些有趣的相似性,但与功能性无关的粟酒裂殖酵母Thi1却发现了更高的相似性。对在prnA基因中定位的许多突变进行测序。这包括一个缺失,该缺失导致prnA特异的mRNA几乎完全丧失,推定的核定位信号发生突变,锌簇第二个环中的脯氨酸变为亮氨酸突变以及因此导致的冷敏感突变。称为“中央区域”。其他完全或部分功能丧失的突变定位在功能未知的区域。我们确定该基因的转录既不受自我调节,也不受碳和/或氮代谢物阻抑的影响。

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