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Generation of xenomitochondrial embryonic stem cells for the production of live xenomitochondrial mice
chapter
posted on 2016-01-01, 00:00 authored by Ian A Trounce, Jessica Ackerley, Matthew McKenzieMatthew McKenzieThe unique features of the mitochondrial genome, such as its high copy number and lack of defined mechanisms of recombination, have hampered efforts to manipulate its sequence to create specific mutations in mouse mtDNA. As such, the generation of in vivo mouse models of mtDNA disease has proved technically challenging. This chapter describes a unique approach to create mitochondrial oxidative phosphorylation (OXPHOS) defects in mouse ES cells by transferring mtDNA from different murid species into Mus musculus domesticus ES cells using cytoplasmic hybrid ("cybrid") fusion. The resulting "xenocybrid" ES cells carry OXPHOS defects of varying severity, and can be utilized to generate live mouse models of mtDNA disease.
History
Title of book
Mitochondrial DNA : methods and protocolsSeries
Methods in molecular biology ; 1351Chapter number
12Pagination
163 - 173Publisher
SpringerPlace of publication
Berlin, GermanyPublisher DOI
eISSN
1940-6029ISBN-13
9781493930395Language
engPublication classification
B Book chapter; B1.1 Book chapterCopyright notice
2016, SpringerExtent
17Editor/Contributor(s)
Matthew McKenzieUsage metrics
Categories
Keywords
Embryonic stem cell sFibroblastsFusionMouseXenocybridAnimalsBlastocystCell FusionCell LineCell NucleusChimeraDNA, MitochondrialDisease Models, AnimalEmbryonic Stem CellsFemaleGene Transfer TechniquesL Cells (Cell Line)MiceMitochondriaMitochondrial DiseasesNuclear Transfer TechniquesNucleic Acid Amplification TechniquesOxidative PhosphorylationScience & TechnologyLife Sciences & BiomedicineBiochemical Research MethodsBiochemistry & Molecular BiologyMITOCHONDRIAL GENOTYPE SEGREGATIONTRANSMITOCHONDRIAL MICEMOUSE MODELDNAMTDNAGENEMUTATIONCHLORAMPHENICOLMICROINJECTIONDYSFUNCTION