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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Society for Biochemistry and Molecular Biology
2009
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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 |
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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 |
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