Kurjan J, Hall B D
Department of Genetics, University of Washington, Seattle, Washington 98195, USA.
Mol Cell Biol. 1982 Dec;2(12):1501-13. doi: 10.1128/mcb.2.12.1501-1513.1982.
The SUP4 tRNA(Tyr) locus in Saccharomyces cerevisiae has been studied by the isolation and characterization of mutations at the SUP4 gene which result in the loss of suppressor function. Most of the mutations act as single-site mutations, whereas about a third of the mutations are deletions of the entire gene. Two meiotic fine-structure maps of the gene were made. The first mapping technique placed 10 mutations plus the sup4+ anticodon on a map by a measurement of levels of recombination between pairs of mutations. The second map utilized a more qualitative estimate of recombination frequency, allowing 69 mutations and the sup4+ anticodon to be mapped. The maps were compared with the physical structure of the gene for the 34 mutations whose nucleotide alteration has been determined by DNA sequencing (Koski et al., Cell 22:415-425, 1980; Kurjan et al., Cell 20:701-709, 1980). Both maps show a good correlation with the physical structure of the gene, even though certain properties of genetic fine-structure maps, such as marker effects and "map expansion," were seen.
通过分离和鉴定酿酒酵母中SUP4基因的突变(这些突变导致抑制功能丧失),对SUP4 tRNA(Tyr)基因座进行了研究。大多数突变表现为单点突变,而约三分之一的突变是整个基因的缺失。构建了该基因的两个减数分裂精细结构图。第一种作图技术通过测量成对突变之间的重组水平,将10个突变加上sup4 +反密码子定位在一张图上。第二张图利用了对重组频率的更定性估计,从而将69个突变和sup4 +反密码子定位。将这些图与34个突变的基因物理结构进行了比较,这些突变的核苷酸改变已通过DNA测序确定(Koski等人,《细胞》22:415 - 425,1980;Kurjan等人,《细胞》20:701 - 709,1980)。尽管观察到了遗传精细结构图的某些特性,如标记效应和“图谱扩展”,但两张图都与基因的物理结构显示出良好的相关性。