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Publication : Gene therapy for progeny of mito-mice carrying pathogenic mtDNA by nuclear transplantation.

First Author  Sato A Year  2005
Journal  Proc Natl Acad Sci U S A Volume  102
Issue  46 Pages  16765-70
PubMed ID  16275929 Mgi Jnum  J:103743
Mgi Id  MGI:3610677 Doi  10.1073/pnas.0506197102
Citation  Sato A, et al. (2005) Gene therapy for progeny of mito-mice carrying pathogenic mtDNA by nuclear transplantation. Proc Natl Acad Sci U S A 102(46):16765-70
abstractText  Pathogenic mutations in mtDNAs have been shown to be responsible for expression of respiration defects and resultant expression of mitochondrial diseases. This study directly addressed the issue of gene therapy of mitochondrial diseases by using nuclear transplantation of zygotes of transmitochondria mice (mito-mice). Mito-mice expressed respiration defects and mitochondrial diseases due to accumulation of mtDNA carrying a large-scale deletion (DeltamtDNA). Second polar bodies were used as biopsy samples for diagnosis of mtDNA genotypes of mito-mouse zygotes. Nuclear transplantation was carried out from mito-mouse zygotes to enucleated normal zygotes and was shown to rescue all of the F(0) progeny from expression of respiration defects throughout their lives. This procedure should be applicable to patients with mitochondrial diseases for preventing their children from developing the diseases.
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