Cargando…

Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks

Analysis of human heart mitochondrial DNA (mtDNA) by electron microscopy and agarose gel electrophoresis revealed a complete absence of the θ-type replication intermediates seen abundantly in mtDNA from all other tissues. Instead only Y- and X-junctional forms were detected after restriction digesti...

Descripción completa

Detalles Bibliográficos
Autores principales: Pohjoismäki, Jaakko L. O., Goffart, Steffi, Tyynismaa, Henna, Willcox, Smaranda, Ide, Tomomi, Kang, Dongchon, Suomalainen, Anu, Karhunen, Pekka J., Griffith, Jack D., Holt, Ian J., Jacobs, Howard T.
Formato: Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755869/
https://www.ncbi.nlm.nih.gov/pubmed/19525233
http://dx.doi.org/10.1074/jbc.M109.016600
_version_ 1782172475787837440
author Pohjoismäki, Jaakko L. O.
Goffart, Steffi
Tyynismaa, Henna
Willcox, Smaranda
Ide, Tomomi
Kang, Dongchon
Suomalainen, Anu
Karhunen, Pekka J.
Griffith, Jack D.
Holt, Ian J.
Jacobs, Howard T.
author_facet Pohjoismäki, Jaakko L. O.
Goffart, Steffi
Tyynismaa, Henna
Willcox, Smaranda
Ide, Tomomi
Kang, Dongchon
Suomalainen, Anu
Karhunen, Pekka J.
Griffith, Jack D.
Holt, Ian J.
Jacobs, Howard T.
author_sort Pohjoismäki, Jaakko L. O.
collection PubMed
description Analysis of human heart mitochondrial DNA (mtDNA) by electron microscopy and agarose gel electrophoresis revealed a complete absence of the θ-type replication intermediates seen abundantly in mtDNA from all other tissues. Instead only Y- and X-junctional forms were detected after restriction digestion. Uncut heart mtDNA was organized in tangled complexes of up to 20 or more genome equivalents, which could be resolved to genomic monomers, dimers, and linear fragments by treatment with the decatenating enzyme topoisomerase IV plus the cruciform-cutting T7 endonuclease I. Human and mouse brain also contained a population of such mtDNA forms, which were absent, however, from mouse, rabbit, or pig heart. Overexpression in transgenic mice of two proteins involved in mtDNA replication, namely human mitochondrial transcription factor A or the mouse Twinkle DNA helicase, generated abundant four-way junctions in mtDNA of heart, brain, and skeletal muscle. The organization of mtDNA of human heart as well as of mouse and human brain in complex junctional networks replicating via a presumed non-θ mechanism is unprecedented in mammals.
format Text
id pubmed-2755869
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher American Society for Biochemistry and Molecular Biology
record_format MEDLINE/PubMed
spelling pubmed-27558692009-10-13 Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks Pohjoismäki, Jaakko L. O. Goffart, Steffi Tyynismaa, Henna Willcox, Smaranda Ide, Tomomi Kang, Dongchon Suomalainen, Anu Karhunen, Pekka J. Griffith, Jack D. Holt, Ian J. Jacobs, Howard T. J Biol Chem DNA: Replication, Repair, Recombination, and Chromosome Dynamics Analysis of human heart mitochondrial DNA (mtDNA) by electron microscopy and agarose gel electrophoresis revealed a complete absence of the θ-type replication intermediates seen abundantly in mtDNA from all other tissues. Instead only Y- and X-junctional forms were detected after restriction digestion. Uncut heart mtDNA was organized in tangled complexes of up to 20 or more genome equivalents, which could be resolved to genomic monomers, dimers, and linear fragments by treatment with the decatenating enzyme topoisomerase IV plus the cruciform-cutting T7 endonuclease I. Human and mouse brain also contained a population of such mtDNA forms, which were absent, however, from mouse, rabbit, or pig heart. Overexpression in transgenic mice of two proteins involved in mtDNA replication, namely human mitochondrial transcription factor A or the mouse Twinkle DNA helicase, generated abundant four-way junctions in mtDNA of heart, brain, and skeletal muscle. The organization of mtDNA of human heart as well as of mouse and human brain in complex junctional networks replicating via a presumed non-θ mechanism is unprecedented in mammals. American Society for Biochemistry and Molecular Biology 2009-08-07 2009-06-12 /pmc/articles/PMC2755869/ /pubmed/19525233 http://dx.doi.org/10.1074/jbc.M109.016600 Text en © 2009 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles
spellingShingle DNA: Replication, Repair, Recombination, and Chromosome Dynamics
Pohjoismäki, Jaakko L. O.
Goffart, Steffi
Tyynismaa, Henna
Willcox, Smaranda
Ide, Tomomi
Kang, Dongchon
Suomalainen, Anu
Karhunen, Pekka J.
Griffith, Jack D.
Holt, Ian J.
Jacobs, Howard T.
Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks
title Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks
title_full Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks
title_fullStr Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks
title_full_unstemmed Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks
title_short Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks
title_sort human heart mitochondrial dna is organized in complex catenated networks containing abundant four-way junctions and replication forks
topic DNA: Replication, Repair, Recombination, and Chromosome Dynamics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755869/
https://www.ncbi.nlm.nih.gov/pubmed/19525233
http://dx.doi.org/10.1074/jbc.M109.016600
work_keys_str_mv AT pohjoismakijaakkolo humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT goffartsteffi humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT tyynismaahenna humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT willcoxsmaranda humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT idetomomi humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT kangdongchon humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT suomalainenanu humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT karhunenpekkaj humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT griffithjackd humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT holtianj humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks
AT jacobshowardt humanheartmitochondrialdnaisorganizedincomplexcatenatednetworkscontainingabundantfourwayjunctionsandreplicationforks