Olive M G, Daugherty J R, Cooper T G
Department of Microbiology and Immunology, University of Tennessee, Memphis 38163.
J Bacteriol. 1991 Jan;173(1):255-61. doi: 10.1128/jb.173.1.255-261.1991.
Several highly inducible enzyme activities are required for the degradation of allantoin in Saccharomyces cerevisiae. Induction of these pathway enzymes has been shown to be regulated at transcription, and response to inducer is lost in dal81 and dal82/durM mutants. The similar phenotypes generated by dal81 and dal82 mutations prompted the question of whether they were allelic. We demonstrated that the DAL81 and DAL82 loci are distinct, unlinked genes situated on chromosomes IX and XIV. DAL82 gene expression did not respond to induction by the allantoin pathway inducer or to nitrogen catabolite repression. Expression was also not significantly affected by mutation of the dal80 locus. From the nucleotide sequence of the DAL82 gene, we deduced that it encodes a protein with a mass of 29,079 Da that may possess the structural motifs expected of a regulatory protein. This protein was shown to be required for the function mediated by the cis-acting upstream induction sequence situated in the 5'-flanking regions of the inducible allantoin pathway genes.
酿酒酵母中尿囊素的降解需要几种高度可诱导的酶活性。这些途径酶的诱导已被证明在转录水平受到调控,并且在dal81和dal82/durM突变体中对诱导剂的反应丧失。dal81和dal82突变产生的相似表型引发了它们是否为等位基因的问题。我们证明DAL81和DAL82位点是位于IX号和XIV号染色体上的不同的、不连锁的基因。DAL82基因的表达对尿囊素途径诱导剂的诱导或氮代谢物阻遏均无反应。dal80位点的突变对其表达也没有显著影响。根据DAL82基因的核苷酸序列,我们推断它编码一种质量为29,079 Da的蛋白质,该蛋白质可能具有调控蛋白预期的结构基序。已证明该蛋白质是位于可诱导尿囊素途径基因5'侧翼区域的顺式作用上游诱导序列介导的功能所必需的。