Maintenance of mitochondrial DNA (mtDNA) during cell division is required for progeny to be respiratory competent. Maintenance involves the replication, repair, assembly, segregation, and partitioning of the mitochondrial nucleoid. MGM101 has been identified as a gene essential for mtDNA maintenance in S. cerevisiae, but its role is unknown. Using liquid chromatography coupled with tandem mass spectrometry, we identified Mgm101p as a component of highly enriched nucleoids, suggesting that it plays a nucleoid-specific role in maintenance. Subcellular fractionation, indirect immunofluorescence and GFP tagging show that Mgm101p is exclusively associated with the mitochondrial nucleoid structure in cells. Furthermore, DNA affinity chromatography of nucleoid extracts indicates that Mgm101p binds to DNA, suggesting that its nucleoid localization is in part due to this activity. Phenotypic analysis of cells containing a temperature sensitive mgm101 allele suggests that Mgm101p is not involved in mtDNA packaging, segregation, partitioning or required for ongoing mtDNA replication. We examined Mgm101p's role in mtDNA repair. As compared with wild-type cells, mgm101 cells were more sensitive to mtDNA damage induced by UV irradiation and were hypersensitive to mtDNA damage induced by gamma rays and H2O2 treatment. Thus, we propose that Mgm101p performs an essential function in the repair of oxidatively damaged mtDNA that is required for the maintenance of the mitochondrial genome.
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19 April 1999
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April 19 1999
Mgm101p Is a Novel Component of the Mitochondrial Nucleoid That Binds DNA and Is Required for the Repair of Oxidatively Damaged Mitochondrial DNA
Shelly Meeusen,
Shelly Meeusen
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
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Quinton Tieu,
Quinton Tieu
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
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Edith Wong,
Edith Wong
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
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Eric Weiss,
Eric Weiss
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
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David Schieltz,
David Schieltz
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
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John R. Yates,
John R. Yates
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
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Jodi Nunnari
Jodi Nunnari
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
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Shelly Meeusen
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
Quinton Tieu
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
Edith Wong
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
Eric Weiss
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
David Schieltz
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
John R. Yates
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
Jodi Nunnari
*Section of Molecular and Cellular Biology, University of California, Davis, California 95616; and ‡The Department of Molecular Biotechnology, University of Washington, School of Medicine, Seattle, Washington 98195
Address correspondence to Jodi Nunnari, Section of Molecular and Cellular Biology, University of California, Davis, CA 95616. Tel.: (530) 754-9774. Fax: (530) 752-7522. E-mail: [email protected]
Eric Weiss' present address is Department of Molecular and Cellular Biology, University of California, Berkeley, CA 94720.
Received:
December 11 1998
Revision Received:
March 04 1999
Online ISSN: 1540-8140
Print ISSN: 0021-9525
1999
J Cell Biol (1999) 145 (2): 291–304.
Article history
Received:
December 11 1998
Revision Received:
March 04 1999
Citation
Shelly Meeusen, Quinton Tieu, Edith Wong, Eric Weiss, David Schieltz, John R. Yates, Jodi Nunnari; Mgm101p Is a Novel Component of the Mitochondrial Nucleoid That Binds DNA and Is Required for the Repair of Oxidatively Damaged Mitochondrial DNA . J Cell Biol 19 April 1999; 145 (2): 291–304. doi: https://doi.org/10.1083/jcb.145.2.291
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