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一个能够抑制酿酒酵母胆碱转运突变体的SCT1基因的分离与鉴定

Isolation and characterization of a SCT1 gene which can suppress a choline-transport mutant of Saccharomyces cerevisiae.

作者信息

Matsushita M, Nikawa J

机构信息

Department of Biochemical Engineering and Science, Faculty of Computer Science and Systems Engineering, Kyushu Institute of Technology, Fukuoka.

出版信息

J Biochem. 1995 Feb;117(2):447-51. doi: 10.1093/jb/117.2.447.

Abstract

The yeast Saccharomyces cerevisiae possesses a choline-transport system encoded by the CTR1 gene. We isolated a yeast gene, SCT1, that can suppress a CTR1 defect when introduced as a multicopy. The SCT1 coding frame is capable of encoding 759 residues with a calculated molecular weight of 85,734. On Northern blot analysis, an RNA species that hybridized with the coding region was detected in the total RNA of the wild-type yeast. The transcription of SCT1 is constitutive. The primary translation product contains three membrane-spanning domains, a PEST-like sequence, and a glutamic acid-rich sequence at the C terminal end. Gene disruption experiments showed that SCT1 is not an essential gene under the standard culture conditions. SCT1 did not suppress a null mutant of ctr1, indicating that a mutant form of choline transporter is necessary for the suppression caused by SCT1.

摘要

酿酒酵母拥有一个由CTR1基因编码的胆碱转运系统。我们分离出一个酵母基因SCT1,当以多拷贝形式导入时,它能够抑制CTR1缺陷。SCT1编码框能够编码759个氨基酸残基,计算分子量为85,734。在Northern印迹分析中,在野生型酵母的总RNA中检测到与编码区杂交的RNA物种。SCT1的转录是组成型的。初级翻译产物包含三个跨膜结构域、一个类PEST序列以及C末端富含谷氨酸的序列。基因破坏实验表明,在标准培养条件下SCT1不是必需基因。SCT1不能抑制ctr1的缺失突变体,这表明胆碱转运蛋白的突变形式对于SCT1引起的抑制作用是必需的。

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