Authors
Daniel Paull, Valentina Emmanuele, Keren A Weiss, Nathan Treff, Latoya Stewart, Haiqing Hua, Matthew Zimmer, David J Kahler, Robin S Goland, Scott A Noggle, Robert Prosser, Michio Hirano, Mark V Sauer, Dieter Egli
Publication date
2013/1/31
Journal
Nature
Volume
493
Issue
7434
Pages
632-637
Publisher
Nature Publishing Group UK
Description
Mitochondrial DNA mutations transmitted maternally within the oocyte cytoplasm often cause life-threatening disorders. Here we explore the use of nuclear genome transfer between unfertilized oocytes of two donors to prevent the transmission of mitochondrial mutations. Nuclear genome transfer did not reduce developmental efficiency to the blastocyst stage, and genome integrity was maintained provided that spontaneous oocyte activation was avoided through the transfer of incompletely assembled spindle–chromosome complexes. Mitochondrial DNA transferred with the nuclear genome was initially detected at levels below 1%, decreasing in blastocysts and stem-cell lines to undetectable levels, and remained undetectable after passaging for more than one year, clonal expansion, differentiation into neurons, cardiomyocytes or β-cells, and after cellular reprogramming. Stem cells and differentiated cells had …
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