Dunon-Bluteau D, Cordonnier A, Brun G
Laboratoire de Biochimie, Institut Curie, Paris, France.
J Mol Biol. 1987 Sep 20;197(2):175-85. doi: 10.1016/0022-2836(87)90116-1.
Conditions for efficient replication in vitro of mitochondrial DNA L strand into H strand products have been established. Gel electrophoresis and hybridization analyses of the products show that neosynthesized H strands are progressively elongated from the D-loop region, and some of them are synthesized as full-length molecules. Evidence for initiation of these H strands de novo is presented. In contrast, there is no detectable L strand synthesis in vitro in this system. This may prove useful for analyzing the distinct molecular mechanisms operating at OH and OL. Use of specific inhibitors indicates that DNA synthesis in the mitochondrial lysate in vitro requires DNA polymerase gamma. These observations support the conclusion that replication in vitro in this system closely resembles the first steps of mitochondrial DNA replication in vivo.
已建立了线粒体DNA轻链在体外高效复制为重链产物的条件。对产物的凝胶电泳和杂交分析表明,新合成的重链从D环区域开始逐渐延长,其中一些以全长分子形式合成。本文提供了这些重链从头起始合成的证据。相比之下,在该系统中体外未检测到轻链合成。这可能有助于分析在重链起点(OH)和轻链起点(OL)处起作用的不同分子机制。使用特异性抑制剂表明,体外线粒体裂解物中的DNA合成需要DNA聚合酶γ。这些观察结果支持以下结论:该系统中的体外复制与体内线粒体DNA复制的第一步非常相似。