Morimoto R, Rabinowitz M
Mol Gen Genet. 1979 Feb 16;170(1):11-23. doi: 10.1007/BF00268577.
A detailed molecular dissection of the yeast mitochondrial genome can be made with restriction endonucleases that generate site-specific cuts in DNA. The ordering of restriction fragments provides the basis of the physical mapping of mitochondrial transcripts and antibiotic resistance (antR) loci, and is a means of analyzing the molecular organization of mtDNA of petite and mit- deletion mutants. We have previously mapped the sites in the mtDNA of yeast strain MH41-7B recognized by the endonucleases Eco RI, Hpa I, Hind III, Bam HI, Sal I, Pst I, and Hha I, providing a total of 41 cleavage sites. We have now mapped the sites recognized by the endonucleases Xba I, Hinc II, Bgl II, Pvu II, Xho I, and Sst I, which make 6, 13, 5, 6, 2, and 2 cuts, respectively. Fragment maps for each of these endonuclease sites were derived by analysis of the products of double-enzyme digests and by hybridization of 3H-cRNA probes transcribed from low-kinetic-complexity petite mtDNAs to restriction fragments generated by various combinations of enzymes.
利用能在DNA上产生位点特异性切割的限制性内切酶,可以对酵母线粒体基因组进行详细的分子剖析。限制性片段的排序为线粒体转录本和抗生素抗性(antR)位点的物理图谱绘制提供了基础,也是分析小菌落和线粒体缺失突变体的线粒体DNA分子组织的一种方法。我们之前已对酵母菌株MH41 - 7B线粒体DNA中被内切酶Eco RI、Hpa I、Hind III、Bam HI、Sal I、Pst I和Hha I识别的位点进行了图谱绘制,总共确定了41个切割位点。我们现在已对被内切酶Xba I、Hinc II、Bgl II、Pvu II、Xho I和Sst I识别的位点进行了图谱绘制,这些酶分别能产生6、13、5、6、2和2个切割位点。通过对双酶切产物的分析,以及将从低动力学复杂性小菌落线粒体DNA转录而来的3H - cRNA探针与由各种酶组合产生的限制性片段进行杂交,得出了每个这些内切酶位点的片段图谱。