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Mapping major replication origins on the rice plastid DNA

机译:在水稻质体DNA上定位主要复制起点

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To maintain and to differentiate into various plastid lineages, replication of the plastid DNA (ptDNA) and division of the plastid must take place. However, replication initiation of the ptDNA has been less understood. The present study describes identification of the initiation region (origin) of ptDNA replication in the rice cultured cells. RNA-primed newly replicated DNA strands pulse-labeled with bromodeoxyuridine were isolated and size-fractionated. Locations of these nascent strands on the ptDNA determined the two major origin regions around the 3' region of each 23S rDNA in the inverted repeats (IR_A and IR_B). Two-dimensional agarose gel electrophoresis of the replication intermediates suggested that replication from each origin proceeds bidirectionally. This contrasted to replication by the double D - loop mechanism.
机译:为了维持并分化成各种质体谱系,必须进行质体DNA(ptDNA)的复制和质体的分裂。但是,对ptDNA的复制起始了解得很少。本研究描述了水稻培养细胞中ptDNA复制起始区域(起源)的鉴定。分离出用溴脱氧尿苷脉冲标记的RNA引发的新复制的DNA链,并进行大小分级。这些新生链在ptDNA上的位置决定了反向重复序列(IR_A和IR_B)中每个23S rDNA 3'区域周围的两个主要来源区域。复制中间体的二维琼脂糖凝胶电泳表明,每个起点的复制都是双向进行的。这与通过双重D循环机制进行复制形成对比。

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