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DNA polymerases delta and epsilon are required for chromosomal replication in Saccharomyces cerevisiae.

机译:DNA聚合酶δ和ε是酿酒酵母中染色体复制所必需的。

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摘要

Three DNA polymerases, alpha, delta, and epsilon are required for viability in Saccharomyces cerevisiae. We have investigated whether DNA polymerases epsilon and delta are required for DNA replication. Two temperature-sensitive mutations in the POL2 gene, encoding DNA polymerase epsilon, have been identified by using the plasmid shuffle technique. Alkaline sucrose gradient analysis of DNA synthesis products in the mutant strains shows that no chromosomal-size DNA is formed after shift of an asynchronous culture to the nonpermissive temperature. The only DNA synthesis observed is a reduced quantity of short DNA fragments. The DNA profiles of replication intermediates from these mutants are similar to those observed with DNA synthesized in mutants deficient in DNA polymerase alpha under the same conditions. The finding that DNA replication stops upon shift to the nonpermissive temperature in both DNA polymerase alpha- and DNA polymerase epsilon- deficient strains shows that both DNA polymerases are involved in elongation. By contrast, previous studies on pol3 mutants, deficient in DNA polymerase delta, suggested that there was considerable residual DNA synthesis at the nonpermissive temperature. We have reinvestigated the nature of DNA synthesis in pol3 mutants. We find that pol3 strains are defective in the synthesis of chromosomal-size DNA at the restrictive temperature after release from a hydroxyurea block. These results demonstrate that yeast DNA polymerase delta is also required at the replication fork.
机译:酿酒酵母中的生存力需要三种DNA聚合酶,α,δ和ε。我们已经研究了DNA复制是否需要DNA聚合酶epsilon和delta。 POL2基因中的两个温度敏感突变编码DNA聚合酶epsilon,已通过使用质粒改组技术进行了鉴定。突变菌株中DNA合成产物的碱性蔗糖梯度分析表明,将异步培养物转移到非允许温度后,没有形成染色体大小的DNA。观察到的唯一DNA合成是数量减少的短DNA片段。这些突变体的复制中间体的DNA谱与在相同条件下在DNA聚合酶α缺乏的突变体中合成的DNA观察到的DNA谱相似。在DNA聚合酶α和DNA聚合酶ε缺陷型菌株中,DNA复制都在转变到非许可温度时停止,这表明DNA聚合酶都参与了延伸。相比之下,先前对pol3突变体(DNA聚合酶δ不足)的研究表明,在非允许温度下仍有大量残留的DNA合成。我们已经重新研究了pol3突变体中DNA合成的本质。我们发现pol3菌株从羟基脲嵌段释放后,在限制性温度下在染色体大小的DNA合成中存在缺陷。这些结果表明复制叉处也需要酵母DNA聚合酶δ。

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