Cunningham T S, Cooper T G
Department of Microbiology and Immunology, University of Tennessee, Memphis 38163.
Mol Cell Biol. 1991 Dec;11(12):6205-15. doi: 10.1128/mcb.11.12.6205-6215.1991.
We have cloned the negative regulatory gene (DAL80) of the allantoin catabolic pathway, characterized its structure, and determined the physiological conditions that control DAL80 expression and its influence on the expression of nitrogen catabolic genes. Disruption of the DAL80 gene demonstrated that it regulates multiple nitrogen catabolic pathways. Inducer-independent expression was observed for the allantoin pathway genes DAL7 and DUR1,2, as well as the UGA1 gene required for gamma-aminobutyrate catabolism in the disruption mutant. DAL80 transcription was itself highly sensitive to nitrogen catabolite repression (NCR), and its promoter contained 12 sequences homologous to the NCR-sensitive UASNTR. The deduced DAL80 protein structure contains zinc finger and coiled-coil motifs. The DAL80 zinc finger motif possessed high homology to the transcriptional activator proteins required for expression of NCR-sensitive genes in fungi and the yeast GLN3 gene product required for functioning of the NCR-sensitive DAL UASNTR. It was also homologous to the three GATAA-binding proteins reported to be transcriptional activators in avian and mammalian tissues. The latter correlations raise the possibility that both positive and negative regulators of allantoin pathway transcription may bind to similar sequences.
我们克隆了尿囊素分解代谢途径的负调控基因(DAL80),对其结构进行了表征,并确定了控制DAL80表达的生理条件及其对氮分解代谢基因表达的影响。DAL80基因的破坏表明它调节多种氮分解代谢途径。在破坏突变体中,观察到尿囊素途径基因DAL7和DUR1,2以及γ-氨基丁酸分解代谢所需的UGA1基因的非诱导型表达。DAL80转录本身对氮分解代谢物阻遏(NCR)高度敏感,其启动子包含12个与NCR敏感的UASNTR同源的序列。推导的DAL80蛋白结构包含锌指和卷曲螺旋基序。DAL80锌指基序与真菌中NCR敏感基因表达所需的转录激活蛋白以及NCR敏感的DAL UASNTR功能所需的酵母GLN3基因产物具有高度同源性。它也与报道为鸟类和哺乳动物组织中的转录激活因子的三种GATAA结合蛋白同源。后一种相关性增加了尿囊素途径转录的正调控因子和负调控因子可能与相似序列结合的可能性。