摘要
目的:研究酵母RAD24L基因功能,克隆人类同源物。方法:分离RAD24基因区域rad24L突变株,以人的cDNA表达文库转化突变株,筛选回复表型;大剂量X线照射观察细胞周期。结果:rad24L对紫外线敏感,从转化文库后的回复表型中克隆出人类hR24L全长cDNA。结论:克隆的人类DNA修复基因hR24L,它能校正rad24L的突变表型,参与细胞周期检定点调控。
Objective:To study the function of RAD24L of S.cerevisiae and clone human functional homologue. Methods:The UV sensitive mutant rad24L was isolated by plasmid shuffling. Then, transformation of rad24L was performed with human cDNA expression library to screen for reversion phenotype. The cell cycle was studied by X ray irradiation. Results:The mutant rad24L was obtained and a full length cDNA was cloned from reversion phenotype by transformation with human expression library. Conclusion:Human functional homologue of RAD24L was cloned. The hR24L which corrected the phenotype of rad24L mutant is involved in cell cycle checkpoint control.
出处
《北京医科大学学报》
CSCD
1999年第3期269-273,共5页
Journal of Peking University(Health Sciences)
基金
国家自然科学基金
国家高技术发展计划青年基金
关键词
酵母菌
调控
DNA修复基因
突变分析
细胞周期
Saccharomyces, cerevisiae/genet Gene library DNA mutational analysis Cell cycle Genetic complementation test