Naumovski L, Friedberg E C
Mol Cell Biol. 1984 Feb;4(2):290-5. doi: 10.1128/mcb.4.2.290-295.1984.
A plasmid (pNF2000) containing a 9.7-kilobase pair DNA insert that complements the UV sensitivity of rad2-1, rad2-2, and rad2-4 mutants of Saccharomyces cerevisiae has been isolated from a yeast genomic library. Genetic analysis of strains derived by transformation of rad2 mutants with an integrating plasmid containing a 9.3-kilobase pair fragment from pNF2000 shows that the fragment integrates exclusively at the chromosomal rad2 gene. We therefore conclude that this plasmid contains the RAD2 gene. The 9.3-kilobase pair fragment was partially digested with Sau3A and cloned into a multicopy yeast vector designed for easy retrieval of Sau3A inserts. The smallest subclone that retains the RAD2 gene is 4.5 kilobase pairs. This fragment was partially digested with Sau3A and cloned into an integrating plasmid. These plasmids were isolated and integrated into a heterozygous rad2/RAD2 strain. Plasmids containing internal fragments of the RAD2 gene were identified because they yielded UV-sensitive transformants due to disruption of the RAD2 gene. Sporulation of diploids transformed with integrating plasmids containing internal fragments of RAD2 gave rise to four viable haploids per tetrad, indicating that unlike the RAD3 gene of S. cerevisiae, the RAD2 gene is not essential for the viability of haploid cells under normal growth conditions. Measurements of the RNA transcript by RNA-DNA hybridization with the internal fragment as the probe indicate a size of approximately 3.2 kilobases.
从酵母基因组文库中分离出了一个质粒(pNF2000),其含有一段9.7千碱基对的DNA插入片段,该片段可弥补酿酒酵母rad2-1、rad2-2和rad2-4突变体对紫外线的敏感性。用含有来自pNF2000的9.3千碱基对片段的整合质粒转化rad2突变体所得到的菌株的遗传分析表明,该片段仅整合到染色体rad2基因处。因此,我们得出结论,该质粒含有RAD2基因。用Sau3A对9.3千碱基对片段进行部分酶切,并克隆到一个多拷贝酵母载体中,该载体设计用于方便回收Sau3A插入片段。保留RAD2基因的最小亚克隆为4.5千碱基对。用Sau3A对该片段进行部分酶切,并克隆到一个整合质粒中。分离出这些质粒并将其整合到杂合rad2/RAD2菌株中。含有RAD2基因内部片段的质粒被鉴定出来,因为它们由于RAD2基因的破坏而产生对紫外线敏感的转化体。用含有RAD2内部片段的整合质粒转化的二倍体的孢子形成产生每个四分体四个存活的单倍体,这表明与酿酒酵母的RAD3基因不同,RAD2基因在正常生长条件下对单倍体细胞的存活不是必需的。以内部片段为探针通过RNA-DNA杂交对RNA转录本进行测量,结果表明其大小约为3.2千碱基。