Cummings D J, Belcour L, Grandchamp C
Mol Gen Genet. 1979 Mar 27;171(3):239-50. doi: 10.1007/BF00267578.
Mitochondrial (Mt) DNA from mitochondrial mutants of race s Podospora anserina and from senescent cultures of races s and A was examined. In mutants, we observed that fewer full length circles (31 mu) were present; instead, smaller circles characteristic for each mutant studied were found. Eco R1 digestion of these mutant MtDNAs indicated that in certain mutants, although specific fragments were absent, the total molecular weight of the fragments was not much different than wild-type. The properties of senescent MtDNA was strikingly different from either wild-type or mutant Mt DNA. First, a multimeric set of circular DNA was observed for both race s and A, with a monomeric repeat size of 0.89 mu. These circles ranged in size from 0.89 mu to greater than 20 mu; only one molecule out of some 200 molecules was thought to be of full length (31 mu). Density gradient analysis showed that there were two density species: a majority were at the same density as wild-type (1.694 g/cm3) and a second at 1.699 g/cm3. Most of the circular molecules from MtDNA isolated by either total DNA extraction or by extraction of DNA from isolated mitochondria were contained in the heavy DNA fraction. Eco R1 enzymatic digestion indicated that the light DNA had several fragments (amounting to about 23 x 10(6) daltons) missing, compared with young, wild-type MtDNA. Heavy senescent MtDNA was not cleaved by Eco R1. Analysis with Hae III restriction endonuclease showed also that light senescent MtDNA was missing certain fragments. Heavy MtDNA of average size 20 x 10(6) daltons, yielded only one fragment, 2,500 bp long, by digestion with Hae III restriction endonuclease. Digestion of heavy DNA with Alu I enzyme yielded 10 fragments totalling 2,570 bp. By three criteria, electron-microscopy, Eco R1 and Hae digestion, we conclude that the heavy MtDNA isolated from senescent cultures of Podospora anserina consisted of a monomeric tandemly repeating subunit of about 2,600 bp length. These results on the properties of senescent MtDNA are discussed with regard to the published properties of the rho- mutation in the yeast, S. cerevisiae.
对盘基网柄菌s族线粒体突变体以及s族和A族衰老培养物的线粒体(Mt)DNA进行了检测。在突变体中,我们观察到全长环状物(31μm)较少;相反,发现了所研究的每个突变体特有的较小环状物。对这些突变体MtDNA进行Eco R1酶切表明,在某些突变体中,尽管特定片段缺失,但片段的总分子量与野生型相差不大。衰老MtDNA的性质与野生型或突变体MtDNA明显不同。首先,在s族和A族中均观察到一组多聚体环状DNA,单体重复大小为0.89μm。这些环状物大小从0.89μm到大于20μm不等;在约200个分子中,只有一个分子被认为是全长的(31μm)。密度梯度分析表明有两种密度类型:大多数与野生型密度相同(1.694 g/cm³),另一种密度为1.699 g/cm³。通过总DNA提取或从分离的线粒体中提取DNA而分离出的MtDNA的大多数环状分子都包含在重DNA组分中。Eco R1酶切表明,与年轻的野生型MtDNA相比,轻DNA缺少几个片段(总计约23×10⁶道尔顿)。重的衰老MtDNA不能被Eco R1切割。用Hae III限制性内切酶分析还表明,轻的衰老MtDNA缺少某些片段。平均大小为20×10⁶道尔顿的重MtDNA,用Hae III限制性内切酶消化后仅产生一个2500 bp长的片段。用Alu I酶消化重DNA产生10个片段,总计2570 bp。通过电子显微镜、Eco R1酶切和Hae酶切这三个标准,我们得出结论,从盘基网柄菌衰老培养物中分离出的重MtDNA由一个长度约为2600 bp的单体串联重复亚基组成。关于衰老MtDNA的这些性质的结果,结合酵母酿酒酵母中rho - 突变的已发表性质进行了讨论。