Literature DB >> 20591530

Repeats, longevity and the sources of mtDNA deletions: evidence from 'deletional spectra'.

Xinhong Guo1, Konstantin Yu Popadin, Natalya Markuzon, Yuriy L Orlov, Yevgenya Kraytsberg, Kim J Krishnan, Gábor Zsurka, Douglas M Turnbull, Wolfram S Kunz, Konstantin Khrapko.   

Abstract

Perfect direct repeats and, in particular, the prominent 13 bp repeat, are thought to cause mitochondrial DNA (mtDNA) deletions, which have been associated with the aging process. Accordingly, individuals lacking the 13 bp repeat are highly prevalent among centenarians and overall number of perfect repeats in mammalian mitochondrial genomes negatively correlates with species' longevity. However, detailed examination of the distribution of mtDNA deletions challenges a special role of the 13 bp repeat in generating mtDNA deletions. Instead, deletions appear to depend on long and stable, albeit imperfect, duplexes between distant mtDNA segments. Furthermore, significant dissimilarities in breakpoint distributions suggest that multiple mechanisms are involved in creating mtDNA deletions. Copyright 2010 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20591530      PMCID: PMC2915442          DOI: 10.1016/j.tig.2010.05.006

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  18 in total

Review 1.  Two direct repeats cause most human mtDNA deletions.

Authors:  David C Samuels; Eric A Schon; Patrick F Chinnery
Journal:  Trends Genet       Date:  2004-09       Impact factor: 11.639

Review 2.  Mitochondrial DNA repeats constrain the life span of mammals.

Authors:  David C Samuels
Journal:  Trends Genet       Date:  2004-05       Impact factor: 11.639

Review 3.  Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations.

Authors:  Yevgenya Kraytsberg; Konstantin Khrapko
Journal:  Expert Rev Mol Diagn       Date:  2005-09       Impact factor: 5.225

4.  Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia.

Authors:  J Wanagat; Z Cao; P Pathare; J M Aiken
Journal:  FASEB J       Date:  2001-02       Impact factor: 5.191

5.  An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.

Authors:  M Zeviani; S Servidei; C Gellera; E Bertini; S DiMauro; S DiDonato
Journal:  Nature       Date:  1989-05-25       Impact factor: 49.962

6.  Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

Authors:  J M Shoffner; M T Lott; A S Voljavec; S A Soueidan; D A Costigan; D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

Review 7.  Mitochondrial involvement in temporal lobe epilepsy.

Authors:  Alexei P Kudin; Gábor Zsurka; Christian E Elger; Wolfram S Kunz
Journal:  Exp Neurol       Date:  2009-03-05       Impact factor: 5.330

8.  Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

Authors:  S Mita; R Rizzuto; C T Moraes; S Shanske; E Arnaudo; G M Fabrizi; Y Koga; S DiMauro; E A Schon
Journal:  Nucleic Acids Res       Date:  1990-02-11       Impact factor: 16.971

Review 9.  What causes mitochondrial DNA deletions in human cells?

Authors:  Kim J Krishnan; Amy K Reeve; David C Samuels; Patrick F Chinnery; John K Blackwood; Robert W Taylor; Sjoerd Wanrooij; Johannes N Spelbrink; Robert N Lightowlers; Doug M Turnbull
Journal:  Nat Genet       Date:  2008-03       Impact factor: 38.330

10.  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

View more
  20 in total

Review 1.  Mechanism of homologous recombination and implications for aging-related deletions in mitochondrial DNA.

Authors:  Xin Jie Chen
Journal:  Microbiol Mol Biol Rev       Date:  2013-09       Impact factor: 11.056

2.  ImtRDB: a database and software for mitochondrial imperfect interspersed repeats annotation.

Authors:  Viktor A Shamanskiy; Valeria N Timonina; Konstantin Yu Popadin; Konstantin V Gunbin
Journal:  BMC Genomics       Date:  2019-05-08       Impact factor: 3.969

Review 3.  Mitochondrial dysfunction in neurological disorders with epileptic phenotypes.

Authors:  Gábor Zsurka; Wolfram S Kunz
Journal:  J Bioenerg Biomembr       Date:  2010-12       Impact factor: 2.945

4.  Contingency and selection in mitochondrial genome dynamics.

Authors:  Christopher J Nunn; Sidhartha Goyal
Journal:  Elife       Date:  2022-04-11       Impact factor: 8.713

5.  Transcription could be the key to the selection advantage of mitochondrial deletion mutants in aging.

Authors:  Axel Kowald; Thomas B L Kirkwood
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-03       Impact factor: 11.205

6.  Mitochondrial DNA deletions are associated with non-B DNA conformations.

Authors:  Joana Damas; João Carneiro; Joana Gonçalves; James B Stewart; David C Samuels; António Amorim; Filipe Pereira
Journal:  Nucleic Acids Res       Date:  2012-05-31       Impact factor: 16.971

7.  Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

Authors:  Lakshmi Narayanan Lakshmanan; Jan Gruber; Barry Halliwell; Rudiyanto Gunawan
Journal:  PLoS One       Date:  2012-04-18       Impact factor: 3.240

8.  Mitochondrial genome deletions and minicircles are common in lice (Insecta: Phthiraptera).

Authors:  Stephen L Cameron; Kazunori Yoshizawa; Atsushi Mizukoshi; Michael F Whiting; Kevin P Johnson
Journal:  BMC Genomics       Date:  2011-08-04       Impact factor: 3.969

9.  An appraisal of human mitochondrial DNA instability: new insights into the role of non-canonical DNA structures and sequence motifs.

Authors:  Pedro H Oliveira; Cláudia Lobato da Silva; Joaquim M S Cabral
Journal:  PLoS One       Date:  2013-03-29       Impact factor: 3.240

Review 10.  Mitochondrial dysfunction in aging: Much progress but many unresolved questions.

Authors:  Brendan A I Payne; Patrick F Chinnery
Journal:  Biochim Biophys Acta       Date:  2015-06-04
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.