Abstract:
:The study of pathogenic mitochondrial DNA mutations has, in most cases, relied on the production of transmitochondrial cybrids. Although the procedure to produce such cybrids is well established, it is laborious and cumbersome. Moreover, the mechanical enucleation procedure is inefficient and different techniques have to be used depending on the adherence properties of the cell. To circumvent these difficulties, we developed a chemical enucleation method that can have wide applicability for the production of transmitochondrial cybrids. The method is based on the use of actinomycin D to render the nuclear genome transcription/replication inactive and unable to recover after treatment. Such treated cells are fused to cells devoid of mitochondrial DNA and selected for the presence of a functional oxidative phosphorylation system. Our results showed that 95% of the clones recovered by this procedure are true transmitochondrial cybrids. This method greatly facilitates the production of transmitochondrial cybrids, thereby increasing the number of mtDNA mutations and the recipient cell types that can be studied by this system.
journal_name
Nucleic Acids Resjournal_title
Nucleic acids researchauthors
Bayona-Bafaluy MP,Manfredi G,Moraes CTdoi
10.1093/nar/gng100keywords:
subject
Has Abstractpub_date
2003-08-15 00:00:00pages
e98issue
16eissn
0305-1048issn
1362-4962journal_volume
31pub_type
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