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首页> 外文期刊>Journal of cell biology >EVIDENCE FOR DISCONTINUOUS REPLICATION OF CIRCULAR MITOCHONDRIAL DNA MOLECULES FROM NOVIKOFF RAT ASCITES HEPATOMA CELLS
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EVIDENCE FOR DISCONTINUOUS REPLICATION OF CIRCULAR MITOCHONDRIAL DNA MOLECULES FROM NOVIKOFF RAT ASCITES HEPATOMA CELLS

机译:Novikoff大鼠断续复制圆形线粒体DNA分子的证据

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Double-forked circular molecules of mitochondrial DNA (mtDNA) from rat tissues, indicated by their form and size to be replicative intermediates, are of two structurally distinct classes. Molecules of the first class are totally double stranded. Molecules of the second class are defined by one daughter segment being totally or partially single stranded. Length histograms of daughter segments measuring between 2% and 44% of the total 5-μm molecular contour were constructed from samples of both classes of replicating molecules derived from mtDNA or Novikoff rat ascites hepatoma cells. For single strand-containing molecules, the lengths fell into eight distinct, reproducible groups with mean values separated by 4.1–7.6% of the circular contour length. For totally double stranded molecules, the lengths fell into seven groups, corresponding to seven of the groups found for single strand-containing molecules. These results suggest that along at least 44% of the contour of mtDNA molecules there exist discrete points at which DNA synthesis tends to be arrested. This may indicate that there are pauses in normal mtDNA synthesis. However, as the DNA used in these experiments was isolated from mitochondrial fractions, the findings may indicate that continuation of synthesis beyond specific points on the nucleotide strands requires a factor which is not available after cell disruption.
机译:来自大鼠组织的线粒体DNA(mtDNA)的双叉环状分子,由其形式和大小指示为可复制的中间体,属于两种结构上不同的类别。一流的分子是完全双链的。第二类分子由全部或部分单链的一个子链段定义。从mtDNA或Novikoff大鼠腹水肝细胞瘤细胞的两类复制分子样品中构建了子片段的长度直方图,其子片段的长度在总5μm分子轮廓的2%到44%之间。对于包含单链的分子,长度分为八个不同的,可重复的组,其平均值相隔圆形轮廓长度的4.1–7.6%。对于完全双链的分子,长度分为七个组,对应于含单链分子的七个组。这些结果表明,沿着mtDNA分子轮廓的至少44%,存在离散点,在该点上DNA合成趋于停止。这可能表明正常的mtDNA合成存在暂停。但是,由于这些实验中使用的DNA是从线粒体级分中分离出来的,因此该发现可能表明,要继续合成,超过核苷酸链上的特定点,则需要一个在细胞破裂后无法获得的因子。

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