Altered epigenetic variance in surviving litters from nutritionally restricted lactating primiparous sows
M. D. Vinsky A , G. K. Murdoch A , W. T. Dixon A , M. K. Dyck A and G. R. Foxcroft A BA Swine Reproduction-Development Program, Swine Research and Technology Centre, University of Alberta, Edmonton, Alberta, Canada.
B Corresponding author. Email: george.foxcroft@ualberta.ca
Reproduction, Fertility and Development 19(3) 430-435 https://doi.org/10.1071/RD06082
Submitted: 1 August 2006 Accepted: 15 December 2006 Published: 14 March 2007
Abstract
Feed restriction of primiparous sows during the last week of lactation has been shown to decrease embryonic growth and female embryo survival to Day 30 of gestation. This study sought to determine whether global DNA methylation and epigenetic gene expression of the candidate genes Igf2, Igf2r, and Xist were associated with these treatment effects. Given that these epigenetic traits are expected to be important for embryo viability, changes in variance for these traits at Day 30 were predicted to be reflected in the loss of abnormal embryos at this time. Consistent with this prediction, variance in DNA methylation was reduced (P < 0.001) in Restrict male embryo, and there was a tendency for reduced variance (P < 0.06) in Restrict female embryos. Variation in DNA methylation tended to be correlated (R = 0.42, P < 0.1) with the difference in variance of embryo weights between treatments (P < 0.01), suggesting a relationship between epigenetic changes and embryonic development. Variance in Igf2r expression tended to decrease (P < 0.07) in Restrict female embryos while variance in Xist expression tended to decrease in Restrict male embryos (P < 0.08), suggesting that maternally inherited epigenetic defects may cause female embryonic loss and reduced growth before Day 30 of gestation.
Additional keywords: catabolism, imprinting, pig, real-time polymerase chain reaction, reverse-phase high performance liquid chromatography.
Acknowledgements
We acknowledge the staff of the University of Alberta Swine Research Technology Center for their dedication in maintenance and care of the experimental animals. We are also grateful to Dr Peter Blenis for help with the statistical analysis and Gary Sedgwick and Dr Kelvin Lien for HPLC support. Funding for this work was received from NSERC, AARI, Alberta Pork and Genex Swine Group and through appointment of Dr George Foxcroft to a Canada Research Chair in Swine Reproductive Physiology.
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