4.8 Article

Mitochondrial DNA replication proceeds via a 'bootlace' mechanism involving the incorporation of processed transcripts

期刊

NUCLEIC ACIDS RESEARCH
卷 41, 期 11, 页码 5837-5850

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OXFORD UNIV PRESS
DOI: 10.1093/nar/gkt196

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  1. Cambridge University Commonwealth Trust
  2. Medical Research Council
  3. Academy of Finland
  4. Sigrid Juselius Foundation
  5. Tampere University Hospital Medical Research Fund
  6. Medical Research Council [MC_U105663140, MC_UP_1202/14] Funding Source: researchfish
  7. MRC [MC_UP_1202/14, MC_U105663140] Funding Source: UKRI

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The observation that long tracts of RNA are associated with replicating molecules of mitochondrial DNA (mtDNA) suggests that the mitochondrial genome of mammals is copied by an unorthodox mechanism. Here we show that these RNA-containing species are present in living cells and tissue, based on interstrand cross-linking. Using DNA synthesis in organello, we demonstrate that isolated mitochondria incorporate radiolabeled RNA precursors, as well as DNA precursors, into replicating DNA molecules. RNA-containing replication intermediates are chased into mature mtDNA, to which they are thus in precursor-product relationship. While a DNA chain terminator rapidly blocks the labeling of mitochondrial replication intermediates, an RNA chain terminator does not. Furthermore, processed L-strand transcripts can be recovered from gel-extracted mtDNA replication intermediates. Therefore, instead of concurrent DNA and RNA synthesis, respectively, on the leading and lagging strands, preformed processed RNA is incorporated as a provisional lagging strand during mtDNA replication. These findings indicate that RITOLS is a physiological mechanism of mtDNA replication, and that it involves a 'bootlace' mechanism, in which processed transcripts are successively hybridized to the lagging-strand template, as the replication fork advances.

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