A novel single-cell DNA fingerprinting method successfully distinguishes sibling human embryos
Objective
To validate a novel system for embryonic DNA fingerprinting which can reliably distinguish sibling embryos from each other.
Design
Prospective, randomized, and blinded study.
Setting
Academic center for reproductive medicine.
Patient(s)
Blastomeres were obtained from discarded and transferred embryos from six patients undergoing IVF treatment.
Intervention(s)
None.
Main Outcome Measure(s)
Single lymphocytes from sibling cell lines and blastomeres from sibling day 3 human embryos were evaluated for accurate assignment of relationship using whole genome amplification and single-nucleotide polymorphism microarrays.
Result(s)
Assignment of single-cell relationships was accomplished with 100% accuracy. We also observed complete agreement between the molecular karyotype and DNA fingerprint–based identification of embryos implanted in three clinical IVF cases after multiple embryo transfer.
Conclusion(s)
These data demonstrate the first single-blastomere DNA fingerprinting technology capable of unequivocal discrimination of sibling human embryos.
Key Words: Blastomere, DNA fingerprinting, DNA microarray, single nucleotide polymorphism, whole genome amplification
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N.T., K.M., and R.S. are supported by grants from EMD Serono, Schering Plough, Ferring Pharmaceuticals, and Barr Pharmaceuticals. The spouse of J.S. is an employee of GE Healthcare. B.L. is a consultant and advisory board member for Affymetrix. X.T. has nothing to disclose.
PII: S0015-0282(09)00637-2
doi:10.1016/j.fertnstert.2009.03.067
© 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

