| Literature DB >> 27611966 |
Ning Cheng1,2, Yih-Shan Lo1, Mohammad Israil Ansari1, Kuo-Chieh Ho2, Shih-Tong Jeng2, Na-Sheng Lin1, Hwa Dai1.
Abstract
The currently accepted model of recombination-dependent replication (RDR) in plant mitochondrial DNA (mtDNA) does not clearly explain how RDR progresses and how highly complex mtDNA develops. This study aimed to investigate the correlation between RDR and mtDNA complexity during mitochondrial development in mung bean (Vigna radiata) seed, and the initiation and processing of RDR in plant mitochondria. Flow cytometry, pulsed-field gel electrophoresis, electron microscopy, real-time PCR and biochemical studies were used in this study. The highly dynamic changes in mtDNA complexity correspond to mtDNA RDR activity throughout mitochondrial development. With in vitro freeze-thaw treatment or prolonged in vivo cold incubation, the mtDNA rosette core disappeared and the rosette structure converted to a much longer linear DNA structure. D-loops, Holliday junctions and putative RDR forks often appeared near the rosette cores. We hypothesize that the rosette core may consist of condensed mtDNA and a replication starting sequence, and play an initial and central role in RDR. The satellite cores in the rosette structure may represent the re-initiation sites of mtDNA RDR in the same parental molecule, thereby forming highly complex and giant mitochondrial molecules, representing the RDR intermediates, in vivo.Entities:
Keywords: in vitro mtDNA replication; mitochondrial development; mtDNA complexity; mtDNA rosette; mung bean (Vigna radiata); plant mitochondrial DNA; recombination-dependent replication; rosette core
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Year: 2016 PMID: 27611966 DOI: 10.1111/nph.14158
Source DB: PubMed Journal: New Phytol ISSN: 0028-646X Impact factor: 10.151