Cazelle B, Pokorska A, Hull E, Green P M, Stanway G, Scazzocchio C
Institut de Génétique et Microbiologie, Unité de Recherche Associée au CNRS no. 2225, Université Paris-Sud, Centre Universitaire d'Orsay, France.
Mol Microbiol. 1998 Apr;28(2):355-70. doi: 10.1046/j.1365-2958.1998.00801.x.
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.
prnA基因编码一种转录激活因子,该因子介导构巢曲霉中其他四个参与将脯氨酸作为氮源和/或碳源利用的基因的脯氨酸诱导。在本文中,我们展示了prnA的基因组和cDNA序列以及转录图谱。PrnA蛋白属于转录激活因子的锌双核簇家族。该基因具有显著的内含子-外显子结构,推定的核定位序列和锌簇结构域位于不同的外显子中。尽管该蛋白质序列与酿酒酵母Put3p的同功能蛋白质存在一些有趣的相似性,但与粟酒裂殖酵母功能无关的蛋白质Thi1的相似性更高。对prnA基因中的一些突变位点进行了测序。这包括一个导致prnA特异性mRNA几乎完全丧失的缺失突变、推定核定位信号中的一个突变、锌簇第二个环中脯氨酸到亮氨酸的突变以及所谓“中心区域”的一个冷敏感突变。其他功能完全或部分丧失的突变位于功能未知的区域。我们确定该基因的转录既不受自身调控,也不受碳和/或氮代谢物阻遏的显著影响。