Literature DB >> 33665557

Thermodynamic analysis of DNA hybridization signatures near mitochondrial DNA deletion breakpoints.

Lakshmi Narayanan Lakshmanan1,2, Zhuangli Yee3, Barry Halliwell4, Jan Gruber4,5, Rudiyanto Gunawan6.   

Abstract

Broad evidence in the literature supports double-strand breaks (DSBs) as initiators of mitochondrial DNA (mtDNA) deletion mutations. While DNA misalignment during DSB repair is commonly proposed as the mechanism by which DSBs cause deletion mutations, details such as the specific DNA repair errors are still lacking. Here, we used DNA hybridization thermodynamics to infer the sequence lengths of mtDNA misalignments that are associated with mtDNA deletions. We gathered and analyzed 9,921 previously reported mtDNA deletion breakpoints in human, rhesus monkey, mouse, rat, and Caenorhabditis elegans. Our analysis shows that a large fraction of mtDNA breakpoint positions can be explained by the thermodynamics of short ≤ 5-nt misalignments. The significance of short DNA misalignments supports an important role for erroneous non-homologous and micro-homology-dependent DSB repair in mtDNA deletion formation. The consistency of the results of our analysis across species further suggests a shared mode of mtDNA deletion mutagenesis.
© 2021 The Author(s).

Entities:  

Keywords:  Bioinformatics; Molecular Genetics; Sequence Analysis

Year:  2021        PMID: 33665557      PMCID: PMC7900216          DOI: 10.1016/j.isci.2021.102138

Source DB:  PubMed          Journal:  iScience        ISSN: 2589-0042


  61 in total

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Journal:  Nucleic Acids Res       Date:  1994-03-25       Impact factor: 16.971

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Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

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Journal:  J Biol Chem       Date:  2003-09-17       Impact factor: 5.157

4.  Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion.

Authors:  Stefan Vielhaber; Grazyna Debska-Vielhaber; Viktoriya Peeva; Susanne Schoeler; Alexei P Kudin; Irina Minin; Stefanie Schreiber; Reinhard Dengler; Katja Kollewe; Werner Zuschratter; Cornelia Kornblum; Gábor Zsurka; Wolfram S Kunz
Journal:  Acta Neuropathol       Date:  2012-08-28       Impact factor: 17.088

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Journal:  Nat Genet       Date:  1992-04       Impact factor: 38.330

6.  Translesion Polymerases Drive Microhomology-Mediated Break-Induced Replication Leading to Complex Chromosomal Rearrangements.

Authors:  Cynthia J Sakofsky; Sandeep Ayyar; Angela K Deem; Woo-Hyun Chung; Grzegorz Ira; Anna Malkova
Journal:  Mol Cell       Date:  2015-12-06       Impact factor: 17.970

7.  Mechanism of microhomology-mediated end-joining promoted by human DNA polymerase θ.

Authors:  Tatiana Kent; Gurushankar Chandramouly; Shane Michael McDevitt; Ahmet Y Ozdemir; Richard T Pomerantz
Journal:  Nat Struct Mol Biol       Date:  2015-02-02       Impact factor: 15.369

8.  Intra- and inter-molecular recombination of mitochondrial DNA after in vivo induction of multiple double-strand breaks.

Authors:  Sandra R Bacman; Sion L Williams; Carlos T Moraes
Journal:  Nucleic Acids Res       Date:  2009-05-12       Impact factor: 16.971

9.  High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.

Authors:  Andreas Bender; Kim J Krishnan; Christopher M Morris; Geoffrey A Taylor; Amy K Reeve; Robert H Perry; Evelyn Jaros; Joshua S Hersheson; Joanne Betts; Thomas Klopstock; Robert W Taylor; Douglass M Turnbull
Journal:  Nat Genet       Date:  2006-04-09       Impact factor: 38.330

10.  Microhomology-mediated end joining is the principal mediator of double-strand break repair during mitochondrial DNA lesions.

Authors:  Satish Kumar Tadi; Robin Sebastian; Sumedha Dahal; Ravi K Babu; Bibha Choudhary; Sathees C Raghavan
Journal:  Mol Biol Cell       Date:  2015-11-25       Impact factor: 4.138

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