Ahne F, Baur M, Eckardt-Schupp F
GSF-Forschungszentrum für Umwelt und Gesundheit, Institut für Strahlenbiologie, Neuherberg, Federal Republic of Germany.
Curr Genet. 1992 Oct;22(4):277-82. doi: 10.1007/BF00317921.
The REV2 gene of Saccharomyces cerevisiae was cloned and sequenced; it contains an open reading frame of 1986 bp with a coding potential of 662 amino acids. Interruption of the chromosomal REV2 gene by integrating the URA3 gene coupled with partial deletion of the 3' terminal region produced viable haploid rev2 delta mutants. This indicates that the REV2 gene is non-essential for growth. The rev2 delta mutant is slightly more UV-sensitive than strains carrying various rev2 alleles (rev2-1, rev2x, rad5-1, rad5-8). The putative Rev2 protein is probably a globular protein containing a highly conserved nucleotide-binding site and two zinc-finger domains.
克隆并测序了酿酒酵母的REV2基因;它包含一个1986 bp的开放阅读框,编码潜能为662个氨基酸。通过整合URA3基因并部分缺失3'末端区域来中断染色体REV2基因,产生了可存活的单倍体rev2Δ突变体。这表明REV2基因对于生长不是必需的。rev2Δ突变体比携带各种rev2等位基因(rev2-1、rev2x、rad5-1、rad5-8)的菌株对紫外线稍微更敏感。推测的Rev2蛋白可能是一种含有高度保守核苷酸结合位点和两个锌指结构域的球状蛋白。