Morimoto R, Lewin A, Rabinowitz M
Nucleic Acids Res. 1977 Jul;4(7):2331-51. doi: 10.1093/nar/4.7.2331.
Mitochondrial DNA (mtDNA) from the yeast Saccharomyces cerevisiae was cleaved by restriction endonucleases Eco RI, Hpa I, Bam HI, Hind III, Pst I, and Sal I, yielding 10, 7, 5, 6, 1, and 1 fragments, respectively. A physical ordering of the restriction sites on yeast mtDNA has been derived. Yeast mtDNA cannot be isolated as intact molecules, and it contains nicks and gaps which complicate the use of conventional fragment mapping procedures. Nevertheless, the position of each of the restriction sites was obtained primarily by reciprocal redigestion of isolated restriction fragments. This procedure was supplemented by co-digestion of mtDNA with a multisite enzyme and a single-site enzyme (i.e., Sal I or Pst I) which provided a unique orientation for overlapping fragments cleaved by Sal I or Pst I. The data obtained from these approaches were confirmed by analysis of double and triple enzyme digests. Analysis of partial digest fragments was used for positioning of the smallest Eco RI fragment. A comparison of mtDNA from four grande strains (MH41-7B, 19d, TR3-15A, and MH32-12D) revealed similar, but slightly varying restriction patterns, with an identical genome size for each of approximately 5 X 10(-7) d or 75 kb. A fifth grande strain, D273-10B from S. cerevisiae, revealed restriction patterns different from those of the above strains, with a smaller genome size of 70 kb.
来自酿酒酵母的线粒体DNA(mtDNA)被限制性内切酶Eco RI、Hpa I、Bam HI、Hind III、Pst I和Sal I切割,分别产生10、7、5、6、1和1个片段。已得出酵母mtDNA上限制性酶切位点的物理排序。酵母mtDNA无法作为完整分子分离,并且它含有切口和间隙,这使得传统的片段图谱绘制程序的使用变得复杂。然而,每个限制性酶切位点的位置主要通过对分离的限制性片段进行相互再消化来获得。该程序通过将mtDNA与一种多位点酶和一种单位点酶(即Sal I或Pst I)共同消化来补充,这为被Sal I或Pst I切割的重叠片段提供了独特的方向。通过对双酶切和三酶切消化产物的分析,证实了从这些方法获得的数据。对部分消化片段的分析用于定位最小的Eco RI片段。对四个大菌株(MH41 - 7B、19d、TR3 - 15A和MH32 - 12D)的mtDNA进行比较,发现它们的限制性图谱相似但略有不同,每个菌株的基因组大小相同,约为5×10⁻⁷ d或75 kb。第五个大菌株,来自酿酒酵母的D273 - 10B,其限制性图谱与上述菌株不同,基因组大小为70 kb。