Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions. 2019

Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
Department of Medical Biochemistry and Cell Biology, University of Gothenburg, P.O. Box 440, Gothenburg, SE-405 30, Sweden.

Mitochondrial DNA (mtDNA) deletions are associated with mitochondrial disease, and also accumulate during normal human ageing. The mechanisms underlying mtDNA deletions remain unknown although several models have been proposed. Here we use deep sequencing to characterize abundant mtDNA deletions in patients with mutations in mitochondrial DNA replication factors, and show that these have distinct directionality and repeat characteristics. Furthermore, we recreate the deletion formation process in vitro using only purified mitochondrial proteins and defined DNA templates. Based on our in vivo and in vitro findings, we conclude that mtDNA deletion formation involves copy-choice recombination during replication of the mtDNA light strand.

UI MeSH Term Description Entries
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D004261 DNA Replication The process by which a DNA molecule is duplicated. Autonomous Replication,Replication, Autonomous,Autonomous Replications,DNA Replications,Replication, DNA,Replications, Autonomous,Replications, DNA
D004272 DNA, Mitochondrial Double-stranded DNA of MITOCHONDRIA. In eukaryotes, the mitochondrial GENOME is circular and codes for ribosomal RNAs, transfer RNAs, and about 10 proteins. Mitochondrial DNA,mtDNA
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D015139 Blotting, Southern A method (first developed by E.M. Southern) for detection of DNA that has been electrophoretically separated and immobilized by blotting on nitrocellulose or other type of paper or nylon membrane followed by hybridization with labeled NUCLEIC ACID PROBES. Southern Blotting,Blot, Southern,Southern Blot
D017384 Sequence Deletion Deletion of sequences of nucleic acids from the genetic material of an individual. Deletion Mutation,Deletion Mutations,Deletion, Sequence,Deletions, Sequence,Mutation, Deletion,Mutations, Deletion,Sequence Deletions
D024101 Mitochondrial Proteins Proteins encoded by the mitochondrial genome or proteins encoded by the nuclear genome that are imported to and resident in the MITOCHONDRIA. Proteins, Mitochondrial,Mitochondrial Protein,Protein, Mitochondrial

Related Publications

Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
March 1988, Cell,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
August 1990, Cell,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
June 1994, The EMBO journal,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
November 1994, BioEssays : news and reviews in molecular, cellular and developmental biology,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
June 2017, eLife,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
March 2008, Nature genetics,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
February 2009, Genes & development,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
May 2001, Annals of neurology,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
August 2016, JCI insight,
Örjan Persson, and Yazh Muthukumar, and Swaraj Basu, and Louise Jenninger, and Jay P Uhler, and Anna-Karin Berglund, and Robert McFarland, and Robert W Taylor, and Claes M Gustafsson, and Erik Larsson, and Maria Falkenberg
January 2021, Frontiers in genetics,
Copied contents to your clipboard!