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Epigenetic reprogramming in embryonic and foetal development upon somatic cell nuclear transfer cloning

Department of Biotechnology, Institute for Animal Breeding (FAL), Mariensee, Hoeltystr. 10, 31535 Neustadt, Germany¹ Department of Animal Science/Center Regenerative Biology, University of Connecticut, 1392 Storrs Road, U-4243 Storrs, Connecticut 06269-4243, USA² Department of Biomedical Sciences, University of Guelph, Guelph, Ontario N1G 2W1, Canada and³ Reproductive Technologies Group, AgResearch, Ruakura Research Centre, Hamilton 3240, New Zealand

Correspondence should be addressed to H Niemann; Email: niemann{at}tzv.fal.de

The birth of ‘Dolly’, the first mammal cloned from an adult donor cell, has sparked a flurry of research activities to improve cloning technology and to understand the underlying mechanism of epigenetic reprogramming of the transferred somatic cell nucleus. Especially in ruminants, somatic cell nuclear transfer (SCNT) is frequently associated with pathological changes in the foetal and placental phenotype and has significant consequences for development both before and after birth. The most critical factor is epigenetic reprogramming of the transferred somatic cell nucleus from its differentiated status into the totipotent state of the early embryo. This involves an erasure of the gene expression program of the respective donor cell and the establishment of the well-orchestrated sequence of expression of an estimated number of 10 000–12 000 genes regulating embryonic and foetal development. The following article reviews the present knowledge on the epigenetic reprogramming of the transferred somatic cell nucleus, with emphasis on DNA methylation, imprinting, X-chromosome inactivation and telomere length restoration in bovine development. Additionally, we briefly discuss other approaches towards epigenetic nuclear reprogramming, including the fusion of somatic and embryonic stem cells and the overexpression of genes crucial in the formation and maintenance of the pluripotent status. Improvements in our understanding of this dramatic epigenetic reprogramming event will be instrumental in realising the great potential of SCNT for basic biological research and for various agricultural and biomedical applications.

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