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Impact of whole-genome amplification on the reliability of pre-transfer cattle embryo breeding value estimates
Authors:Habib A Shojaei Saadi  Christian Vigneault  Mehdi Sargolzaei  Dominic Gagné  éric Fournier  Béatrice de Montera  Jacques Chesnais  Patrick Blondin  Claude Robert
Institution:.Laboratory of Functional Genomics of Early Embryonic Development, Institut des nutraceutiques et des aliments fonctionnels, Faculté des sciences de l’agriculture et de l’alimentation, Pavillon des services, Université Laval, Québec, G1V 0A6 Canada ;.L’Alliance Boviteq Inc, 19320 Grand rang St-François, Saint-Hyacinthe, J2T 5H1 Québec Canada ;.L’Alliance Semex Inc, 130 Stone Road West, Guelph, N1G 3Z2 Ontario Canada
Abstract:

Background

Genome-wide profiling of single-nucleotide polymorphisms is receiving increasing attention as a method of pre-implantation genetic diagnosis in humans and of commercial genotyping of pre-transfer embryos in cattle. However, the very small quantity of genomic DNA in biopsy material from early embryos poses daunting technical challenges. A reliable whole-genome amplification (WGA) procedure would greatly facilitate the procedure.

Results

Several PCR-based and non-PCR based WGA technologies, namely multiple displacement amplification, quasi-random primed library synthesis followed by PCR, ligation-mediated PCR, and single-primer isothermal amplification were tested in combination with different DNA extractions protocols for various quantities of genomic DNA inputs. The efficiency of each method was evaluated by comparing the genotypes obtained from 15 cultured cells (representative of an embryonic biopsy) to unamplified reference gDNA. The gDNA input, gDNA extraction method and amplification technology were all found to be critical for successful genome-wide genotyping. The selected WGA platform was then tested on embryo biopsies (n = 226), comparing their results to that of biopsies collected after birth. Although WGA inevitably leads to a random loss of information and to the introduction of erroneous genotypes, following genomic imputation the resulting genetic index of both sources of DNA were highly correlated (r = 0.99, P<0.001).

Conclusion

It is possible to generate high-quality DNA in sufficient quantities for successful genome-wide genotyping starting from an early embryo biopsy. However, imputation from parental and population genotypes is a requirement for completing and correcting genotypic data. Judicious selection of the WGA platform, careful handling of the samples and genomic imputation together, make it possible to perform extremely reliable genomic evaluations for pre-transfer embryos.

Electronic supplementary material

The online version of this article (doi:10.1186/1471-2164-15-889) contains supplementary material, which is available to authorized users.
Keywords:Bovine early embryo  Embryo biopsy  Whole-genome amplification  Genotyping  Genomic breeding value  Genotype imputation  Pre-Implantation genetic diagnosis  Multiple displacement amplification
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