Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouse

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Abstract
In mammals, the maternal and paternal genomes are required for embryonic development1–5. This is due to genomic imprinting which leads to the expression or repression of genes solely on the basis of the parent from which they were inherited6–9 As a result, parthenogenetic embryos die before day 10 of gestation and show limited development of extra-embryonic membranes3,4. Maternal imprinting is established during oogenesis6–11 and is associated with allele specific modifications in DMA methylation. We have investigated epigenetic modifications during oocyte growth using nuclear transfer techniques to produce mature oocytes with maternal chro-matin derived from non-growing oocytes. Parthenogenetic activation of such oocytes leads to the development of normal size fetuses with a well developed placenta on day 13.5 of gestation; three days further than previously recorded for parthenogenetic development. In contrast, after fertilization, only one embryo was recovered on 9.5 days of gestation. Further, in these embryos we investigated the well characterized methylation pattern of the maternally expressed insulin-like growth factor II receptor gene (lgf2r) and found that the pattern of methylation was indeed different to that of fertilized control embryos. Thus, the embryonic phenotypes observed here correlate with changes in epigenetic events that normally occur during oocyte growth.