Weiss W A, Friedberg E C
EMBO J. 1985 Jun;4(6):1575-82. doi: 10.1002/j.1460-2075.1985.tb03819.x.
A plasmid designated pNF101 was isolated by transforming rad10 mutants with a yeast genomic library and screening transformed cells for enhanced resistance to killing by u.v. radiation. Plasmid pNF101 fully complements the u.v. sensitivity of rad10 mutant strains and was shown to contain the RAD10 gene by genetic analysis of integrant strains. The nucleotide sequence of the RAD10 gene was determined. The coding region consists of 195 codons and could encode a polypeptide of calculated mol. wt. 22 616 daltons. RAD10 protein expressed in Escherichia coli maxicells has a mol. wt of approximately 30 kd measured by gel electrophoresis. The RAD10 gene was localized to chromosome XIII of Saccharomyces cerevisiae by hybridization of the cloned gene to yeast chromosomes resolved by electrophoresis, and by genetic analysis.
通过用酵母基因组文库转化rad10突变体并筛选转化细胞以增强对紫外线辐射杀伤的抗性,分离出了一种名为pNF101的质粒。质粒pNF101完全互补rad10突变体菌株的紫外线敏感性,并且通过整合菌株的遗传分析表明其包含RAD10基因。确定了RAD10基因的核苷酸序列。编码区由195个密码子组成,可编码一个计算分子量为22616道尔顿的多肽。在大肠杆菌最大细胞中表达的RAD10蛋白通过凝胶电泳测量其分子量约为30kd。通过将克隆基因与经电泳分离的酵母染色体杂交以及遗传分析,将RAD10基因定位到酿酒酵母的第十三号染色体上。