Mitchell A P
Genetics. 1985 Oct;111(2):243-58. doi: 10.1093/genetics/111.2.243.
Among 41 yeast glutamine auxotrophs, complementation analysis defined a single gene, GLN1, on chromosome 16 between MAK3 and MAK6. Half of the alleles fell into two intragenic complementation classes. No clustering of complementing alleles was found in a fine structure map. Altered glutamine synthetase subunits, including nonsense fragments and charge variants, were identified in several of the mutants, indicating that GLN1 is the structural gene for this enzyme. Negative complementation was observed for almost every allele associated with a protein product and all gln1/+ heterozygotes displayed reduced susceptibility to ammonia repression of the remaining glutamine synthetase activity. This latter observation is explained by the hypothesis that ammonia represses the enzyme only through its metabolism to glutamine. A basis for the two gln1 complementation classes is proposed.
在41个酵母谷氨酰胺营养缺陷型菌株中,互补分析确定了位于第16号染色体上MAK3和MAK6之间的一个单一基因GLN1。一半的等位基因分为两个基因内互补类别。在精细结构图谱中未发现互补等位基因的聚集现象。在几个突变体中鉴定出了改变的谷氨酰胺合成酶亚基,包括无义片段和电荷变体,这表明GLN1是该酶的结构基因。几乎每个与蛋白质产物相关的等位基因都观察到负互补现象,并且所有gln1/+杂合子对剩余谷氨酰胺合成酶活性的氨抑制表现出降低的敏感性。后一观察结果可通过以下假设来解释:氨仅通过其代谢为谷氨酰胺来抑制该酶。提出了两个gln1互补类别的基础。