Lewin A, Morimoto R, Rabinowitz M
Mol Gen Genet. 1978 Jul 25;163(3):257-75. doi: 10.1007/BF00271955.
We have analyzed the restriction digest patterns of the mitochondrial DNA from 41 cytoplasmic petite strains of Saccharomyces cerevisiae, that have been extensively characterized with respect to genetic markers. Each mitochondrial DNA was digested with seven restriction endonucleases (EcoRI, HPaI, HindIII, BamHI, HhaI, SalI, and PstI) which together make 41 cuts in grande mitochondrial DNA and for which we have derived fragment maps. The petite mitochondrial DNAs were also analyzed with HpaII, HaeIII, and AluI, each of which makes more than 80 cleavages in grande mitochondrial DNA. On the basis of the restriction patterns observed (i.e., only one fragment migrating differently from grande for a single deletion, and more than one for multiple deletions) and by comparing petite and grande mitochondrial DNA restriction maps, the petite clones could be classified into two main groups: (1) petites representing a single deletion of grande mitochondrial DNA and (2) petites containing multiple deletions of the grande mitochondrial DNA resulting in rearranged sequences. Single deletion petites may retain a large portion of the grande mitochondrial genome or may be of low kinetic cimplexity. Many petites which are scored as single continuous deletions by genetic criteria were later demonstrated to be internally deleted by restriction endonuclease analysis. Heterogeneous sequences, manifested by the presence of sub-stoichiometric amounts of some restriction fragments, may accompany the single or multiple deletions. Single deletions with heterogeneous sequences remain useful for mapping if the low concentration sequences represent a subset of the stoichiometric bands. Using a group of petites which retain single continuous regions of the grande mitochondrial DNA, we have physically mapped antibiotic resistance and mit- markers to regions of the grande restriction map as follows: C (99.3--1.4 map units)--OXI-1 (2.5--15.7)--OXI-2 (18.5--25)--P (28.1--34.2)--OXI-3 (32.2--61.2--OII (60--62)--COB (64.6--80.8--0I (80.4--85.7)--E (95--98.9).
我们分析了41株酿酒酵母细胞质小菌落菌株线粒体DNA的限制性酶切图谱,这些菌株已通过遗传标记进行了广泛表征。每种线粒体DNA用7种限制性内切酶(EcoRI、HPaI、HindIII、BamHI、HhaI、SalI和PstI)进行消化,这些酶在野生型线粒体DNA中总共产生41个切点,我们据此绘制了片段图谱。小菌落线粒体DNA还用HpaII、HaeIII和AluI进行了分析,每种酶在野生型线粒体DNA中产生80多个切点。根据观察到的限制性图谱(即单个缺失时只有一个片段迁移情况与野生型不同,多个缺失时有多个片段迁移情况不同),并通过比较小菌落和野生型线粒体DNA限制性图谱,小菌落克隆可分为两个主要组:(1)代表野生型线粒体DNA单个缺失的小菌落;(2)包含野生型线粒体DNA多个缺失导致序列重排的小菌落。单个缺失的小菌落可能保留了大部分野生型线粒体基因组,也可能具有低动力学复杂性。许多根据遗传标准被判定为单个连续缺失的小菌落在后来通过限制性内切酶分析被证明是内部缺失。一些限制性片段亚化学计量存在所表现出的异质序列可能伴随单个或多个缺失。如果低浓度序列代表化学计量条带的一个子集,具有异质序列的单个缺失对于图谱绘制仍然有用。使用一组保留野生型线粒体DNA单个连续区域的小菌落,我们已将抗生素抗性和线粒体标记物物理定位到野生型限制性图谱的区域如下:C(99.3 - 1.4图谱单位) - OXI - 1(2.5 - 15.7) - OXI - 2(18.5 - 25) - P(28.1 - 34.2) - OXI - 3(32.2 - 61.2) - OII(60 - 62) - COB(64.6 - 80.8) - OI(80.4 - 85.7) - E(95 - 98.9)。