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使用非变性Southern杂交和二维琼脂糖凝胶检测酿酒酵母端粒复制中的假定中间体。

Use of non-denaturing Southern hybridization and two dimensional agarose gels to detect putative intermediates in telomere replication in Saccharomyces cerevisiae.

作者信息

Wellinger R J, Wolf A J, Zakian V A

机构信息

Fred Hutchinson Cancer Research Center, Seattle, WA 98104.

出版信息

Chromosoma. 1992;102(1 Suppl):S150-6. doi: 10.1007/BF02451800.

Abstract

Telomeres are required for the complete duplication of the ends of linear chromosomes. Saccharomyces telomeres bear approximately 350 bps of C1-3A/TG1-3 sequences. Previous work using non-denaturing Southern blotting has demonstrated the cell cycle controlled appearance of single stranded TG1-3 tails on chromosomal and plasmid telomeres (Wellinger et al. submitted). Furthermore it was shown that short linear plasmids carrying an origin of replication derived from 2 microns DNA can circularize at the time of telomere replication (Wellinger et al. submitted). Here we demonstrate that those loci previously shown to acquire single stranded tails are indeed telomeres and that single stranded TG1-3 cannot be observed in non-telomeric C1-3A/TG1-3-tracts. Moreover, we demonstrate that the formation of circular DNA by short linear plasmids is not restricted to plasmids containing a 2 microns origin of replication but can also be detected for plasmids containing ARS1.

摘要

端粒对于线性染色体末端的完整复制是必需的。酿酒酵母的端粒带有约350个碱基对的C1-3A/TG1-3序列。先前使用非变性Southern印迹法的研究表明,在染色体和质粒端粒上,单链TG1-3尾巴的出现受细胞周期控制(韦林格等人提交)。此外,研究表明,携带源自2μm DNA的复制起点的短线性质粒在端粒复制时可以环化(韦林格等人提交)。在这里,我们证明,先前显示会获得单链尾巴的那些位点确实是端粒,并且在非端粒的C1-3A/TG1-3片段中无法观察到单链TG1-3。此外,我们证明,短线性质粒形成环状DNA并不局限于含有2μm复制起点的质粒,对于含有ARS1的质粒也能检测到。

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