Single-stranded regions in yeast mitochondrial DNA revealed by pulsed-field gel electrophoresis.

R Maleszka
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引用次数: 0

Abstract

The Klenow fragment of E. coli DNA polymerase together with pulsed-field gel electrophoresis (PFGE) have been used to investigate the presence of single-stranded DNA (ssDNA) regions in yeast (Torulopsis glabrata) DNA. Electrophoretic profiles of total DNA from Rho+ (wild type) and Rho0 (no mitochondrial DNA) strains demonstrate that this method mediates the incorporation of labelled dATP into mitochondrial DNA (mtDNA), but not into chromosomal DNA. The majority of ssDNA (> 62%) has been found associated with the electrophoretically inert component, localized on the top of PFGE gels. Treatment with single-stranded nucleases allows the resolution of this immobile fraction into fast migrating, linear molecules of a heterogeneous size. The possibility that single-stranded tracts and their recombinogenic properties are responsible for the trapping of DNA in pulsed-field gels is discussed.

酵母线粒体DNA单链区域的脉冲场凝胶电泳研究。
利用大肠杆菌DNA聚合酶的Klenow片段和脉冲场凝胶电泳(PFGE)技术研究了酵母(Torulopsis glabrata) DNA单链DNA (ssDNA)区域的存在。Rho+(野生型)和Rho0(无线粒体DNA)菌株的总DNA电泳图谱表明,该方法介导了标记的dATP与线粒体DNA (mtDNA)的结合,而不是与染色体DNA的结合。大多数ssDNA(> 62%)与定位在PFGE凝胶顶部的电泳惰性成分有关。用单链核酸酶处理可以将这种不动的组分分解成快速迁移的、不均匀大小的线性分子。讨论了单链链束及其重组特性在脉冲场凝胶中捕获DNA的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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