Literature DB >> 17666405

The yeast Holliday junction resolvase, CCE1, can restore wild-type mitochondrial DNA to human cells carrying rearranged mitochondrial DNA.

Hiroshi Sembongi1, Miriam Di Re, Monika Bokori-Brown, Ian J Holt.   

Abstract

Rearrangements of mitochondrial DNA (mtDNA) are a well-recognized cause of human disease; deletions are more frequent, but duplications are more readily transmitted to offspring. In theory, partial duplications of mtDNA can be resolved to partially deleted and wild-type (WT) molecules, via homologous recombination. Therefore, the yeast CCE1 gene, encoding a Holliday junction resolvase, was introduced into cells carrying partially duplicated or partially triplicated mtDNA. Some cell lines carrying the CCE1 gene had substantial amounts of WT mtDNA suggesting that the enzyme can mediate intramolecular recombination in human mitochondria. However, high levels of expression of CCE1 frequently led to mtDNA loss, and so it is necessary to strictly regulate the expression of CCE1 in human cells to ensure the selection and maintenance of WT mtDNA.

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Year:  2007        PMID: 17666405     DOI: 10.1093/hmg/ddm182

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  7 in total

1.  Overexpression of MTERFD1 or MTERFD3 impairs the completion of mitochondrial DNA replication.

Authors:  Anne K Hyvärinen; Jaakko L O Pohjoismäki; Ian J Holt; Howard T Jacobs
Journal:  Mol Biol Rep       Date:  2010-06-25       Impact factor: 2.316

Review 2.  Minimizing the damage: repair pathways keep mitochondrial DNA intact.

Authors:  Lawrence Kazak; Aurelio Reyes; Ian J Holt
Journal:  Nat Rev Mol Cell Biol       Date:  2012-09-20       Impact factor: 94.444

Review 3.  The potential of mitochondrial genome engineering.

Authors:  Pedro Silva-Pinheiro; Michal Minczuk
Journal:  Nat Rev Genet       Date:  2021-12-02       Impact factor: 53.242

4.  Overexpression of DNA polymerase zeta reduces the mitochondrial mutability caused by pathological mutations in DNA polymerase gamma in yeast.

Authors:  Enrico Baruffini; Fausta Serafini; Iliana Ferrero; Tiziana Lodi
Journal:  PLoS One       Date:  2012-03-28       Impact factor: 3.240

5.  Near-complete elimination of mutant mtDNA by iterative or dynamic dose-controlled treatment with mtZFNs.

Authors:  Payam A Gammage; Edoardo Gaude; Lindsey Van Haute; Pedro Rebelo-Guiomar; Christopher B Jackson; Joanna Rorbach; Marcin L Pekalski; Alan J Robinson; Marine Charpentier; Jean-Paul Concordet; Christian Frezza; Michal Minczuk
Journal:  Nucleic Acids Res       Date:  2016-07-27       Impact factor: 16.971

Review 6.  The road to rack and ruin: selecting deleterious mitochondrial DNA variants.

Authors:  Ian J Holt; Dave Speijer; Thomas B L Kirkwood
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-07-05       Impact factor: 6.237

7.  Members of the RAD52 Epistasis Group Contribute to Mitochondrial Homologous Recombination and Double-Strand Break Repair in Saccharomyces cerevisiae.

Authors:  Alexis Stein; Lidza Kalifa; Elaine A Sia
Journal:  PLoS Genet       Date:  2015-11-05       Impact factor: 5.917

  7 in total

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