Literature DB >> 9242913

Mitochondrial DNA maintenance in vertebrates.

G S Shadel1, D A Clayton.   

Abstract

The discovery that mutations in mitochondrial DNA (mtDNA) can be pathogenic in humans has increased interest in understanding mtDNA maintenance. The functional state of mtDNA requires a great number of factors for gene expression, DNA replication, and DNA repair. These processes are ultimately controlled by the cell nucleus, because the requisite proteins are all encoded by nuclear genes and imported into the mitochondrion. DNA replication and transcription are linked in vertebrate mitochondria because RNA transcripts initiated at the light-strand promoter are the primers for mtDNA replication at the heavy-strand origin. Study of this transcription-primed DNA replication mechanism has led to isolation of key factors involved in mtDNA replication and transcription and to elucidation of unique nucleic acid structures formed at this origin. Because features of a transcription-primed mechanism appear to be conserved in vertebrates, a general model for initiation of vertebrate heavy-strand DNA synthesis is proposed. In many organisms, mtDNA maintenance requires not only faithful mtDNA replication, but also mtDNA repair and recombination. The extent to which these latter two processes are involved in mtDNA maintenance in vertebrates is also appraised.

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Year:  1997        PMID: 9242913     DOI: 10.1146/annurev.biochem.66.1.409

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  277 in total

1.  Mechanisms of human mitochondrial DNA maintenance: the determining role of primary sequence and length over function.

Authors:  C T Moraes; L Kenyon; H Hao
Journal:  Mol Biol Cell       Date:  1999-10       Impact factor: 4.138

Review 2.  Yeast as a model for human mtDNA replication.

Authors:  G S Shadel
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

3.  Replication and preferential inheritance of hypersuppressive petite mitochondrial DNA.

Authors:  D M MacAlpine; J Kolesar; K Okamoto; R A Butow; P S Perlman
Journal:  EMBO J       Date:  2001-04-02       Impact factor: 11.598

4.  Mitochondrial and mitochondrial-related nuclear genetic function in rabbit urinary bladder following reversal of outlet obstruction.

Authors:  C A Nevel-McGarvey; D Rohrmann; R M Levin; A P Hudson
Journal:  Mol Cell Biochem       Date:  1999-07       Impact factor: 3.396

5.  Stability of the mitochondrial genome requires an amino-terminal domain of yeast mitochondrial RNA polymerase.

Authors:  Y Wang; G S Shadel
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

6.  Genome signature comparisons among prokaryote, plasmid, and mitochondrial DNA.

Authors:  A Campbell; J Mrázek; S Karlin
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

Review 7.  Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.

Authors:  A Brega; J Narula; E Arbustini
Journal:  J Nucl Cardiol       Date:  2001 Jan-Feb       Impact factor: 5.952

8.  Slipped-strand mispairing at noncontiguous repeats in Poecilia reticulata: a model for minisatellite birth.

Authors:  J S Taylor; F Breden
Journal:  Genetics       Date:  2000-07       Impact factor: 4.562

9.  A human mitochondrial transcription factor is related to RNA adenine methyltransferases and binds S-adenosylmethionine.

Authors:  Vicki McCulloch; Bonnie L Seidel-Rogol; Gerald S Shadel
Journal:  Mol Cell Biol       Date:  2002-02       Impact factor: 4.272

10.  Developmentally-regulated packaging of mitochondrial DNA by the HMG-box protein mtTFA during Xenopus oogenesis.

Authors:  E L Shen; D F Bogenhagen
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

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