Literature DB >> 17698960

Yeast aconitase binds and provides metabolically coupled protection to mitochondrial DNA.

Xin Jie Chen1, Xiaowen Wang, Ronald A Butow.   

Abstract

Aconitase (Aco1p) is a multifunctional protein: It is an enzyme of the tricarboxylic acid cycle. In animal cells, Aco1p also is a cytosolic protein binding to mRNAs to regulate iron metabolism. In yeast, Aco1p was identified as a component of mtDNA nucleoids. Here we show that yeast Aco1p protects mtDNA from excessive accumulation of point mutations and ssDNA breaks and suppresses reductive recombination of mtDNA. Aconitase binds to both ds- and ssDNA, with a preference for GC-containing sequences. Therefore, mitochondria are opportunistic organelles that seize proteins, such as metabolic enzymes, for construction of the nucleoid, an mtDNA maintenance/segregation apparatus.

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Year:  2007        PMID: 17698960      PMCID: PMC1959452          DOI: 10.1073/pnas.0703078104

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  41 in total

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Journal:  Biochemistry       Date:  1974-07-30       Impact factor: 3.162

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Journal:  Nucleic Acids Res       Date:  1982-11-11       Impact factor: 16.971

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Authors:  Joseph M Bateman; Philip S Perlman; Ronald A Butow
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Authors:  F Sor; H Fukuhara
Journal:  Nucleic Acids Res       Date:  1984-11-26       Impact factor: 16.971

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Authors:  A L Greenleaf; J L Kelly; I R Lehman
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

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  32 in total

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7.  Suppression of metabolic defects of yeast isocitrate dehydrogenase and aconitase mutants by loss of citrate synthase.

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8.  Assembly of the iron-binding protein frataxin in Saccharomyces cerevisiae responds to dynamic changes in mitochondrial iron influx and stress level.

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9.  Mitochondria-targeted Ogg1 and aconitase-2 prevent oxidant-induced mitochondrial DNA damage in alveolar epithelial cells.

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10.  Mitochondrial nucleoids undergo remodeling in response to metabolic cues.

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