Details

Autor(en) / Beteiligte

• Kang, Eunju
• Wu, Jun
• Gutierrez, Nuria Marti
• Koski, Amy
• Tippner-Hedges, Rebecca
• Agaronyan, Karen
• Platero-Luengo, Aida
• Martinez-Redondo, Paloma
• Ma, Hong
• Lee, Yeonmi
• Hayama, Tomonari
• Van Dyken, Crystal
• Wang, Xinjian
• Luo, Shiyu
• Ahmed, Riffat
• Li, Ying
• Ji, Dongmei
• Kayali, Refik
• Cinnioglu, Cengiz
• Olson, Susan
• Jensen, Jeffrey
• Battaglia, David
• Lee, David
• Wu, Diana
• Huang, Taosheng
• Wolf, Don P
• Temiakov, Dmitry
• Belmonte, Juan Carlos Izpisua
• Amato, Paula
• Mitalipov, Shoukhrat

Titel

Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations

Ist Teil von

• Nature (London), 2016-12, Vol.540 (7632), p.270-275

Ort / Verlag

England: Nature Publishing Group

Erscheinungsjahr

2016

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Maternally inherited mitochondrial (mt)DNA mutations can cause fatal or severely debilitating syndromes in children, with disease severity dependent on the specific gene mutation and the ratio of mutant to wild-type mtDNA (heteroplasmy) in each cell and tissue. Pathogenic mtDNA mutations are relatively common, with an estimated 778 affected children born each year in the United States. Mitochondrial replacement therapies or techniques (MRT) circumventing mother-to-child mtDNA disease transmission involve replacement of oocyte maternal mtDNA. Here we report MRT outcomes in several families with common mtDNA syndromes. The mother's oocytes were of normal quality and mutation levels correlated with those in existing children. Efficient replacement of oocyte mutant mtDNA was performed by spindle transfer, resulting in embryos containing >99% donor mtDNA. Donor mtDNA was stably maintained in embryonic stem cells (ES cells) derived from most embryos. However, some ES cell lines demonstrated gradual loss of donor mtDNA and reversal to the maternal haplotype. In evaluating donor-to-maternal mtDNA interactions, it seems that compatibility relates to mtDNA replication efficiency rather than to mismatch or oxidative phosphorylation dysfunction. We identify a polymorphism within the conserved sequence box II region of the D-loop as a plausible cause of preferential replication of specific mtDNA haplotypes. In addition, some haplotypes confer proliferative and growth advantages to cells. Hence, we propose a matching paradigm for selecting compatible donor mtDNA for MRT.