Electron micrographs of the linear mtDNA from Tetrahymena pyriformis strain GL show linear molecules with a duplex 'eye' of variable size in the middle. This indicates that replication of this DNA starts near the middle of the molecule and proceeds bidirectionally to the ends, as previously shown for the mtDNA of strain ST (Arnberg, A.C., Van Bruggen, E.F.J., Clegg, R.A., Upholt, W.B. and Borst, P. (1974) Biochim. Biophys. Acta 361, 266-276). The mtDNAs of these two strains have little base sequence homology beyond the ribosomal RNA cistron (Goldbach, R.W., Bollen-De Boer, J.E., Van Bruggen, E.F.J. and Borst, P. (1978) Biochim. Biophys. Acta 521, 187-197). 2. Electron micrographs of mtDNA from strain ST, spread under non-denaturing conditions, contain only molecules with fully duplex ends. mtDNA spread under conditions of early denaturation contains duplex loops on one end (40% of all molecules) or both ends (37%). The loops are stable to partial denaturation and vary in size from 0.15 to approximately 1.0 micron, most loops measuring 0.25--0.40 micron. No loops are formed with single-stranded DNA under analogous conditions and we conclude from this result that loop formation is based on the presence of straight, rather than inverted, duplications near the ends. 3. When full-length 3H-labelled mtDNA from strain ST, 32P-labelled at the 5'-termini with T4 polynucleotide kinase, was sedimented in alkaline sucrose gradients, greater than 70% of the 3H and less than 30% of the 32P cosedimented with full-length molecules; the remaining 32P sedimented heterogeneously and predominantly with the DNA less than 10% the size of intact single strands. Brief incubations of full-length mtDNA with DNA polymerase I from Escherichia coli and labelled dNTPs at 15 degrees C did not lead to preferential labelling of terminal EcoRI fragments of the DNA. From these results we infer that the DNA contains nicks or gaps near the termini and that these are not bordered by free 3'-OH groups. 4. A model is presented in which straight sequence repetitions at the termini of Tetrahymena pyriformis mtDNA are involved in the later stages of replication. This model can also account for the pronounced terminal heterogeneity previously observed in this DNA.
摘要
梨形四膜虫GL株系的线性线粒体DNA(mtDNA)的电子显微镜照片显示,线性分子在中间有大小可变的双链“眼”。这表明该DNA的复制始于分子中部附近,并双向延伸至末端,正如之前对ST株系的mtDNA所显示的那样(Arnberg, A.C., Van Bruggen, E.F.J., Clegg, R.A., Upholt, W.B.和Borst, P. (1974) Biochim. Biophys. Acta 361, 266 - 276)。这两个株系的mtDNA除了核糖体RNA顺反子外,碱基序列同源性很低(Goldbach, R.W., Bollen-De Boer, J.E., Van Bruggen, E.F.J.和Borst, P. (1978) Biochim. Biophys. Acta 521, 187 - 197)。2. 在非变性条件下铺展的ST株系mtDNA的电子显微镜照片仅显示出双链末端的分子。在早期变性条件下铺展的mtDNA在一端(占所有分子的40%)或两端(占37%)含有双链环。这些环对部分变性稳定,大小从0.15微米到约1.0微米不等,大多数环的大小为0.25 - 0.40微米。在类似条件下单链DNA不形成环,基于这一结果我们得出结论,环的形成是由于末端附近存在正向而非反向重复序列。3. 当用T4多核苷酸激酶在5'末端进行32P标记的ST株系全长3H标记的mtDNA在碱性蔗糖梯度中沉降时,超过70%的3H与全长分子共沉降,而不到30%的32P与全长分子共沉降;其余的32P不均匀沉降,主要与大小小于完整单链10%的DNA共沉降。在15℃下用大肠杆菌DNA聚合酶I和标记的dNTP对全长mtDNA进行短暂孵育,不会导致DNA末端EcoRI片段的优先标记。从这些结果我们推断,该DNA在末端附近含有切口或缺口,且这些切口或缺口不以游离的3'-OH基团为边界。4. 提出了一个模型,其中梨形四膜虫mtDNA末端的正向序列重复参与复制的后期阶段。该模型也可以解释此前在这种DNA中观察到的明显的末端异质性。