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Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation

Mitochondrial DNA (mtDNA) sequence variants segregate in mutation and tissue-specific manners, but the mechanisms remain unknown. The segregation pattern of pathogenic mtDNA mutations is a major determinant of the onset and severity of disease. Using a heteroplasmic mouse model, we demonstrate that...

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Detalles Bibliográficos
Autores principales: Jokinen, Riikka, Marttinen, Paula, Sandell, Helen Katarin, Manninen, Tuula, Teerenhovi, Heli, Wai, Timothy, Teoli, Daniella, Loredo-Osti, J. C., Shoubridge, Eric A., Battersby, Brendan J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954831/
https://www.ncbi.nlm.nih.gov/pubmed/20976251
http://dx.doi.org/10.1371/journal.pgen.1001161
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author Jokinen, Riikka
Marttinen, Paula
Sandell, Helen Katarin
Manninen, Tuula
Teerenhovi, Heli
Wai, Timothy
Teoli, Daniella
Loredo-Osti, J. C.
Shoubridge, Eric A.
Battersby, Brendan J.
author_facet Jokinen, Riikka
Marttinen, Paula
Sandell, Helen Katarin
Manninen, Tuula
Teerenhovi, Heli
Wai, Timothy
Teoli, Daniella
Loredo-Osti, J. C.
Shoubridge, Eric A.
Battersby, Brendan J.
author_sort Jokinen, Riikka
collection PubMed
description Mitochondrial DNA (mtDNA) sequence variants segregate in mutation and tissue-specific manners, but the mechanisms remain unknown. The segregation pattern of pathogenic mtDNA mutations is a major determinant of the onset and severity of disease. Using a heteroplasmic mouse model, we demonstrate that Gimap3, an outer mitochondrial membrane GTPase, is a critical regulator of this process in leukocytes. Gimap3 is important for T cell development and survival, suggesting that leukocyte survival may be a key factor in the genetic regulation of mtDNA sequence variants and in modulating human mitochondrial diseases.
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spelling pubmed-29548312010-10-25 Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation Jokinen, Riikka Marttinen, Paula Sandell, Helen Katarin Manninen, Tuula Teerenhovi, Heli Wai, Timothy Teoli, Daniella Loredo-Osti, J. C. Shoubridge, Eric A. Battersby, Brendan J. PLoS Genet Research Article Mitochondrial DNA (mtDNA) sequence variants segregate in mutation and tissue-specific manners, but the mechanisms remain unknown. The segregation pattern of pathogenic mtDNA mutations is a major determinant of the onset and severity of disease. Using a heteroplasmic mouse model, we demonstrate that Gimap3, an outer mitochondrial membrane GTPase, is a critical regulator of this process in leukocytes. Gimap3 is important for T cell development and survival, suggesting that leukocyte survival may be a key factor in the genetic regulation of mtDNA sequence variants and in modulating human mitochondrial diseases. Public Library of Science 2010-10-14 /pmc/articles/PMC2954831/ /pubmed/20976251 http://dx.doi.org/10.1371/journal.pgen.1001161 Text en Jokinen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jokinen, Riikka
Marttinen, Paula
Sandell, Helen Katarin
Manninen, Tuula
Teerenhovi, Heli
Wai, Timothy
Teoli, Daniella
Loredo-Osti, J. C.
Shoubridge, Eric A.
Battersby, Brendan J.
Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation
title Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation
title_full Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation
title_fullStr Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation
title_full_unstemmed Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation
title_short Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation
title_sort gimap3 regulates tissue-specific mitochondrial dna segregation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954831/
https://www.ncbi.nlm.nih.gov/pubmed/20976251
http://dx.doi.org/10.1371/journal.pgen.1001161
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