A spindle transfer (more properly "spindle-chromosomal complex transfer") is a genetic manipulation technique where the donor's mitochondrial DNA is not transferred to the receiving egg. It may be used to treat mitochondrial diseases.
Polarized light microscopy spindle imaging and manipulation first were reported (Nature Biotechnology 2000;18(2)223-5) by a team then at the Woods Hole Marine Biological Laboratory and Women and Infants Hospital Division of Reproductive Medicine and IVF (5). They reported 100% spindle enucleation efficiency with transfer of few mitochondria in the karyoplasts of oocytes from various mammalian species. In an article published in Nature online on 26 August 2009, a team in Oregon headed by Dr. Tachibana made the report of the transfer of maternal DNA without any mitochondrial DNA included in a laboratory monkey. This has the implication that any genetic problems which may be transferred from mother to offspring through mitochondrial DNA can be avoided. Teams from the Oregon National Primate Research Center, the Oregon Stem Cell Center and the Departments of Obstetrics and Gynecology, and Molecular and Medical Genetics at the Oregon Health and Science University were all credited in the study.
The 2009 experiment was extended and led to live births. In the latest study (published in Nature in October 2012), the offspring were reported as being alive and well at three years old, and the team conducted a follow-up experiment using human eggs and DNA. Dr. Mitalipov, a development biologist at Oregon Health & Science University, and his team retrieved more than 100 eggs from seven volunteers, who ranged in age from 21 years to 32 years. Of these eggs, 65 were used in the spindle-transfer experiment, while 33 served as non-manipulated controls. Both groups were fertilized by sperm in a lab dish, and their fertilization rate was shown to be roughly the same at more than 70%.
The technique involves taking nuclear DNA from an egg cell and transferring that DNA into another egg cell, leaving the defective mitochondrial DNA behind. The cell is then implanted using in-vitro fertilization techniques. The final mitochondrial DNA, however, is from the receiving egg cell, causing the original donor's mitochondrial DNA to not be passed on to the eventual offspring.
Genetic analysis may then be utilized to confirm that the mother's mitochondrial DNA is not part of the final DNA makeup.
The implications is that a mother who has one of the 150 or so documented syndromes or diseases due to a mitchondral DNA aberration would be able to, using this technique, have children without the mitochondrial issues. This type of human genetic engineering is already being used on a small scale to allow infertile women with genetic defects in their mitochondria to have children.
- Masahito Tachibana, M; Michelle Sparman, Hathaitip Sritanaudomchai, Hong Ma, Lisa Clepper, Joy Woodward, Ying Li, Cathy Ramsey, Olena Kolotushkina & Shoukhrat Mitalipov (17 September 2009). "Mitochondrial gene replacement in primate offspring and embryonic stem cells". Nature 461 (7262): 367–372. doi:10.1038/nature08368. PMC 2774772. PMID 19710649.
- Naik, Gautam (24 October 2012). "DNA Switch Shows Promise Against Genetic Disease". Wall Street Journal. Retrieved 27 November 2012.
- "Genetically altered babies born". BBC News. 2001-05-04. Retrieved 2008-04-26.
5. Liu L,Oldenbourg R, Trimarchi J, Keefe DL. A reliable, non invasive technique for spindle imaging and enucleation of mammalian oocytes. Nature Biotechnology 2000;18(2)223-5.