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Vertebrate reproductive science and technology
RESEARCH ARTICLE

37 LIMITATION OF BOVINE OOPLASM IN REPROGRAMMING OF PORCINE SOMATIC CELLS

O. Østrup A , F. Strejcek B , I. Petrovicova B , M. Morovic B , N. Laurincikova B , A. Lucas-Hahn C , B. Petersen C , H. Niemann C , J. Laurincik B and P. Hyttel A
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A University of Copenhagen, Frederiksberg, Denmark;

B Constantine the Philosopher University, Nitra, Slovakia;

C Friedrich-Loeffler Institute, Mariensee, Germany

Reproduction, Fertility and Development 23(1) 125-125 https://doi.org/10.1071/RDv23n1Ab37
Published: 7 December 2010

Abstract

Ooplasm posses several, undefined factors allowing for reprogramming of somatic genome into pluripotent state. However, it is presently unknown if and to what extent the ooplasm is able to interact with a transferred somatic cell from another species in the context of interspecies somatic cell nuclear transfer (SCNT). The 1-cell stage embryos were processed at different time points (2, 4, 8, and 12 h post-activation) for detailed nuclear and nucleolar analysis by TEM, and immunofluorescence for visualisation of nucleolar proteins related to transcription (UBF) and processing (fibrillarin). The embryos produced by SCNT of porcine fibroblast into non-activated bovine ooplasm were compared to bovine parthenogenetic counterparts. In the absence of morphological remodelling features (premature chromatin condensation, nuclear envelope break-down), intergeneric embryos showed bovine nuclear and nucleolar precursor body (NPB) morphology. The somatic cell introduced into the bovine ooplasm displayed intranuclear activity at the post-translational level signalling a universal function of ooplasmic factors. The lack of distinct UBF localization in intergeneric embryos, however, suggests failures in sequence-specific interactions between the ooplasm and transferred cell from another genus. We conclude that sperm or a somatic cell of the same species is required for successful embryonic development.

Clonet MRTN-CT-2006-035468; MedRat LSHG-CT-2006-518240; PluriSys FP7-HEALTH-2007-223485; DFG, Alexander von Humboldt fellowship, VEGA 1/0057/08; VEGA 1/0012/10.