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Cloning of Saccharomyces cerevisiae DNA replication genes: isolation of the CDC8 gene and two genes that compensate for the cdc8-1 mutation

机译:酿酒酵母DNA复制基因的克隆:CDC8基因和两个补偿cdc8-1突变的基因的分离

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摘要

The CDC8 gene, whose product is required for DNA replication in Saccharomyces cerevisiae, has been isolated on recombinant plasmids. The yeast vector YCp50 bearing the yeast ARS1, CEN4, and URA3 sequences, to provide for replication, stability, and selection, respectively, was used to prepare a recombinant plasmid pool containing the entire yeast genome. Plasmids capable of complementing the temperature-sensitive cdc8-1 mutation were isolated by transformation of a cdc8-1 mutant and selection for clones able to grow at the nonpermissive temperature. The entire complementing activity is carried on a 0.75-kilobase fragment, as revealed by deletion mapping. This fragment lies 1 kilobase downstream from the well-characterized sup4 gene, a gene known to be genetically linked to CDC8, thus confirming that the cloned gene corresponds to the chromosomal CDC8 gene. Two additional recombinant plasmids that complement the cdc8-1 mutation but that do not contain the 0.75-kilobase fragment or any flanking DNA were also identified in this study. These plasmids may contain genes that compensate for the lack of CDC8 gene product.
机译:已在重组质粒上分离出CDC8基因,该产物是在酿酒酵母中进行DNA复制所需的产物。分别带有酵母ARS1,CEN4和URA3序列的酵母载体YCp50用于提供复制,稳定性和选择,用于制备包含整个酵母基因组的重组质粒库。通过转化cdc8-1突变体并选择能够在非容许温度下生长的克隆来分离能够互补温度敏感cdc8-1突变的质粒。如缺失图谱所揭示的,整个互补活性在0.75碱基对的片段上进行。该片段位于公认的与CDC8遗传相连的基因sup4基因的下游1 kb,因此证实了克隆的基因与染色体CDC8基因相对应。在这项研究中,还鉴定了另外两个互补于cdc8-1突变但不包含0.75碱基碱基片段或任何侧翼DNA的重组质粒。这些质粒可能包含补偿CDC8基因产物缺乏的基因。

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  • 作者单位
  • 年度 1983
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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