Budd M E, Campbell J L
Braun Laboratories, California Institute of Technology, Pasadena 91125, USA.
Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7642-6. doi: 10.1073/pnas.92.17.7642.
A yeast gene has been identified by screening for DNA replication mutants using a permeabilized cell replication assay. The mutant is temperature sensitive for growth and shows a cell cycle phenotype typical of DNA replication mutants. RNA synthesis is normal in the mutant but DNA synthesis ceases upon shift to the nonpermissive temperature. The DNA2 gene was cloned by complementation of the dna2ts gene phenotype. The gene is essential for viability. The gene encodes a 172-kDa protein with characteristic DNA helicase motifs. A hemagglutinin epitope-Dna2 fusion protein was prepared and purified by conventional and immunoaffinity chromatography. The purified protein is a DNA-dependent ATPase and has 3' to 5' DNA helicase activity specific for forked substrates. A nuclease activity that endonucleolytically cleaves DNA molecules having a single-stranded 5' tail adjacent to a duplex region copurifies through all steps with the fusion protein.
通过使用通透细胞复制测定法筛选DNA复制突变体,已鉴定出一个酵母基因。该突变体对温度敏感,表现出典型的DNA复制突变体的细胞周期表型。突变体中的RNA合成正常,但转移到非允许温度后DNA合成停止。通过对dna2ts基因表型的互补作用克隆了DNA2基因。该基因对生存力至关重要。该基因编码一种具有特征性DNA解旋酶基序的172 kDa蛋白质。制备了血凝素表位-Dna2融合蛋白,并通过常规和免疫亲和层析进行纯化。纯化后的蛋白质是一种依赖DNA的ATP酶,对叉状底物具有3'至5' DNA解旋酶活性。一种核酸酶活性,可内切切割在双链区域相邻处具有单链5'尾巴的DNA分子,在所有步骤中都与融合蛋白共纯化。