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DNA拓扑异构酶活性作为DNA复制及核糖体RNA转录的旋转体的必要性。

Need for DNA topoisomerase activity as a swivel for DNA replication for transcription of ribosomal RNA.

作者信息

Brill S J, DiNardo S, Voelkel-Meiman K, Sternglanz R

出版信息

Nature. 1987;326(6111):414-6. doi: 10.1038/326414a0.

Abstract

Yeast strains with mutations in the genes for DNA topoisomerases I and II have been identified previously in both Saccharomyces cerevisiae and Schizosaccharomyces pombe. The topoisomerase II mutants (top2) are conditional-lethal temperature-sensitive (ts) mutants. They are defective in the termination of DNA replication and the segregation of daughter chromosomes, but otherwise appear to replicate and transcribe DNA normally. Topoisomerase I mutants (top1), including strains with null mutations are viable and exhibit no obvious growth defects, demonstrating that DNA topoisomerase I is not essential for viability in yeast. In contrast to the single mutants, top1 top2 ts double mutants from both Schizosaccharomyces pombe and Saccharomyces cerevisiae grow poorly at the permissive temperature and stop growth rapidly at the non-permissive temperature. Here we report that DNA and ribosomal RNA synthesis are drastically inhibited in an S. cerevisiae top1 top2 ts double mutant at the restrictive temperature, but that the rate of poly(A)+ RNA synthesis is reduced only about threefold and transfer DNA synthesis remains relatively normal. The results suggest that DNA replication and at least ribosomal RNA synthesis require an active topoisomerase, presumably to act as a swivel to relieve torsional stress, and that either topoisomerase can perform the required function (except in termination of DNA replication where topoisomerase II is required).

摘要

先前已在酿酒酵母和粟酒裂殖酵母中鉴定出DNA拓扑异构酶I和II基因发生突变的酵母菌株。拓扑异构酶II突变体(top2)是条件致死的温度敏感(ts)突变体。它们在DNA复制的终止和子染色体的分离方面存在缺陷,但在其他方面似乎能正常复制和转录DNA。拓扑异构酶I突变体(top1),包括具有无效突变的菌株是可存活的,并且没有表现出明显的生长缺陷,这表明DNA拓扑异构酶I对于酵母的生存力不是必需的。与单突变体不同,来自粟酒裂殖酵母和酿酒酵母的top1 top2 ts双突变体在允许温度下生长不良,在非允许温度下迅速停止生长。在此我们报告,在限制温度下,酿酒酵母top1 top2 ts双突变体中的DNA和核糖体RNA合成受到严重抑制,但聚腺苷酸(poly(A)+)RNA合成速率仅降低约三倍,转移DNA合成仍相对正常。结果表明,DNA复制和至少核糖体RNA合成需要一种活跃的拓扑异构酶,推测其作为一个旋转体来缓解扭转应力,并且任何一种拓扑异构酶都可以执行所需功能(除了在DNA复制终止时需要拓扑异构酶II)。

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