Fu Y H, Marzluf G A
Department of Biochemistry, Ohio State University, Columbus 43210.
J Bacteriol. 1988 Feb;170(2):657-61. doi: 10.1128/jb.170.2.657-661.1988.
In Neurospora crassa, the expression of nit-3, the structural gene which encodes nitrate reductase, is highly regulated and requires both nitrate induction and nitrogen catabolite derepression. The major nitrogen regulatory gene, nit-2, acts in a positive fashion to turn on the expression of nit-3 and other nitrogen-related genes during nitrogen derepression. A second regulatory gene, designated nmr, acts in a negative fashion to repress the expression of nitrate reductase and related enzymes, and nmr mutants are partially insensitive to nitrogen repression. Using cloned genes as specific hybridization probes, we demonstrated that nmr does not affect the transcription of nit-2 but does appear to control nit-3 gene expression. Unlike nmr+ expression, nit-3 expression occurred to some degree even under nitrogen repression conditions in nmr mutant cells. In wild-type cells, nitrate reductase gene expression was dependent upon the presence of nitrate as an inducer. In sharp contrast, nit-3 mRNA expression occurred to a full extent in three different nit-3 mutants, even in the complete absence of any added inducer. Similarly, a nit-1 mutant which was devoid of nitrate reductase activity because it lacked an essential molybdenum cofactor expressed nit-3 without a requirement for induction by nitrate. These results suggest that nitrate reductase autogenously regulates its own expression and that this control is exerted at the transcriptional level.
在粗糙脉孢菌中,编码硝酸还原酶的结构基因nit-3的表达受到高度调控,既需要硝酸盐诱导,也需要氮代谢物阻遏解除。主要的氮调节基因nit-2以正向方式起作用,在氮阻遏解除期间开启nit-3和其他氮相关基因的表达。另一个调节基因,命名为nmr,以负向方式起作用,抑制硝酸还原酶和相关酶的表达,nmr突变体对氮阻遏部分不敏感。使用克隆基因作为特异性杂交探针,我们证明nmr不影响nit-2的转录,但似乎确实控制nit-3基因的表达。与nmr+的表达不同,即使在nmr突变体细胞的氮阻遏条件下,nit-3的表达也会在一定程度上发生。在野生型细胞中,硝酸还原酶基因的表达依赖于硝酸盐作为诱导剂的存在。与之形成鲜明对比的是,在三种不同的nit-3突变体中,即使完全没有添加任何诱导剂,nit-3 mRNA的表达也能充分发生。同样,一个nit-1突变体由于缺乏必需的钼辅因子而没有硝酸还原酶活性,但它表达nit-3时不需要硝酸盐诱导。这些结果表明,硝酸还原酶自主调节其自身的表达,并且这种控制是在转录水平上发挥作用的。