Solomon N A, Wright M B, Chang S, Buckley A M, Dumas L B, Gaber R F
Department of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, IL 60208.
Yeast. 1992 Apr;8(4):273-89. doi: 10.1002/yea.320080405.
Two Saccharomyces cerevisiae genes previously unknown to be required for DNA synthesis have been identified by screening a collection of temperature-sensitive mutants. The effects of mutations in DNA43 and DNA52 on the rate of S phase DNA synthesis were detected by monitoring DNA synthesis in synchronous populations that were obtained by isopycnic density centrifugation. dna43-1 and dna52-1 cells undergo cell-cycle arrest at the restrictive temperature (37 degrees C), exhibiting a large-budded terminal phenotype; the nuclei of arrested cells are located at the neck of the bud and have failed to undergo DNA replication. These phenotypes suggest that DNA43 and DNA52 are required for entry into or completion of S phase. DNA43 and DNA52 were cloned by their abilities to suppress the temperature-sensitive lethal phenotypes of dna43-1 and dna52-1 cells, respectively. DNA sequence analysis suggested that DNA43 and DNA52 encode proteins of 59.6 and 80.6 kDa, respectively. Both DNA43 and DNA52 are essential for viability and genetic mapping experiments indicate that they represent previously unidentified genes: DNA43 is located on chromosome IX, 32 cM distal from his5 and DNA52 is located on chromosome IV, 0.9 cM from cdc34.
通过筛选一组温度敏感型突变体,鉴定出了两个先前未知参与DNA合成所需的酿酒酵母基因。通过监测等密度离心获得的同步群体中的DNA合成,检测了DNA43和DNA52突变对S期DNA合成速率的影响。dna43-1和dna52-1细胞在限制温度(37℃)下发生细胞周期停滞,表现出大芽的终末表型;停滞细胞的细胞核位于芽颈处,且未能进行DNA复制。这些表型表明DNA43和DNA52是进入S期或完成S期所必需的。DNA43和DNA52分别通过抑制dna43-1和dna52-1细胞的温度敏感致死表型的能力进行克隆。DNA序列分析表明,DNA43和DNA52分别编码59.6 kDa和80.6 kDa的蛋白质。DNA43和DNA52对生存力都是必需的,遗传定位实验表明它们代表先前未鉴定的基因:DNA43位于IX号染色体上,距离his5 32 cM,DNA52位于IV号染色体上,距离cdc34 0.9 cM。