Morrison A, Christensen R B, Alley J, Beck A K, Bernstine E G, Lemontt J F, Lawrence C W
Department of Biophysics, School of Medicine, University of Rochester, New York 14642.
J Bacteriol. 1989 Oct;171(10):5659-67. doi: 10.1128/jb.171.10.5659-5667.1989.
We have cloned the REV3 gene of Saccharomyces cerevisiae by complementation of the rev3 defect in UV-induced mutagenesis. The nucleotide sequence of this gene encodes a predicted protein of Mr 172,956 showing significant sequence similarity to Epstein-Barr virus DNA polymerase and to other members of a class of DNA polymerases including human DNA polymerase alpha and yeast DNA polymerase I. REV3 protein shows less sequence identity, and presumably a more distant evolutionary relationship, to the latter two enzymes than they do to each other. Haploids carrying a complete deletion of REV3 are viable. We suggest that induced mutagenesis in S. cerevisiae depends on a specialized DNA polymerase that is not required for other replicative processes. REV3 is located 2.8 centimorgans from CDC60, on chromosome XVI.
我们通过互补紫外线诱导诱变中的rev3缺陷,克隆了酿酒酵母的REV3基因。该基因的核苷酸序列编码一个预测的蛋白质,分子量为172,956,与爱泼斯坦-巴尔病毒DNA聚合酶以及包括人类DNA聚合酶α和酵母DNA聚合酶I在内的一类DNA聚合酶的其他成员具有显著的序列相似性。与后两种酶相比,REV3蛋白与它们彼此之间的序列同一性更低,推测其进化关系更远。携带REV3完全缺失的单倍体是可存活的。我们认为酿酒酵母中的诱导诱变依赖于一种专门的DNA聚合酶,而其他复制过程不需要这种酶。REV3位于第十六号染色体上,距离CDC60有2.8厘摩。