Author
Listed:
- Lyndsey Craven
(Mitochondrial Research Group, Institute for Ageing and Health,)
- Helen A. Tuppen
(Mitochondrial Research Group, Institute for Ageing and Health,)
- Gareth D. Greggains
(Newcastle Fertility Centre, International Centre for Life,
Institute for Ageing and Health, International Centre for Life,)
- Stephen J. Harbottle
(Newcastle Fertility Centre, International Centre for Life,)
- Julie L. Murphy
(Mitochondrial Research Group, Institute for Ageing and Health,)
- Lynsey M. Cree
(Mitochondrial Research Group, Institute for Ageing and Health,)
- Alison P. Murdoch
(Newcastle Fertility Centre, International Centre for Life,
North East England Stem Cell Institute (NESCI), Bioscience Centre, International Centre for Life, Newcastle University, Newcastle upon Tyne NE1 4EP, UK)
- Patrick F. Chinnery
(Mitochondrial Research Group, Institute for Ageing and Health,)
- Robert W. Taylor
(Mitochondrial Research Group, Institute for Ageing and Health,)
- Robert N. Lightowlers
(Mitochondrial Research Group, Institute for Ageing and Health,)
- Mary Herbert
(Newcastle Fertility Centre, International Centre for Life,
Institute for Ageing and Health, International Centre for Life,
North East England Stem Cell Institute (NESCI), Bioscience Centre, International Centre for Life, Newcastle University, Newcastle upon Tyne NE1 4EP, UK)
- Douglass M. Turnbull
(Mitochondrial Research Group, Institute for Ageing and Health,
Newcastle University Centre for Brain Ageing and Vitality, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne NE2 4HH, UK
North East England Stem Cell Institute (NESCI), Bioscience Centre, International Centre for Life, Newcastle University, Newcastle upon Tyne NE1 4EP, UK)
Abstract
mtDNA replacement Mitochondrial DNA (mtDNA) mutations passed down from a mother to offspring are a common cause of genetic disease, including neurological, muscle and heart problems, deafness and type 2 diabetes. It was shown recently in non-human primates that nuclear transfer techniques can prevent their transmission. Now, that proof-of-principle work has been extended to human embryos (see News, http://go.nature.com/xqgWXf ). A multi-department team based at Newcastle University transferred pronuclei between human zygotes, and obtained onward development to the blastocyst stage in vitro. Carry-over of donor zygote mtDNA is minimal, so the technique could potentially prevent the transmission of mtDNA disease in humans.
Suggested Citation
Lyndsey Craven & Helen A. Tuppen & Gareth D. Greggains & Stephen J. Harbottle & Julie L. Murphy & Lynsey M. Cree & Alison P. Murdoch & Patrick F. Chinnery & Robert W. Taylor & Robert N. Lightowlers & , 2010.
"Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease,"
Nature, Nature, vol. 465(7294), pages 82-85, May.
Handle:
RePEc:nat:nature:v:465:y:2010:i:7294:d:10.1038_nature08958
DOI: 10.1038/nature08958
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