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Biology of Reproduction 66, 629-634 (2002)
© 2002 Society for the Study of Reproduction, Inc.


Regular Article

Activation of the Ribosomal RNA Genes Late in the Third Cell Cycle of Porcine Embryos1

Dorthe Viuff2,,a, Torben Grevea, Peter Holmc, Henrik Callesenc, Poul Hyttelb, and Preben D. Thomsenb

a Departments of Clinical Studies, Reproduction, b Anatomy and Physiology, Royal Veterinary and Agricultural University, 1870 Frederiksberg C, Denmark c Department of Animal Breeding and Genetics, Danish Institute of Agricultural Sciences, 8830 Tjele, Denmark

In porcine embryos, nucleoli are first observed during the third postfertilization cell cycle, i.e., at the 4-cell stage. However, direct studies of the initiation of rRNA transcription have not been reported. This transcription was investigated in the present study by simultaneous visualization of the rRNA genes and the rRNA by fluorescent in situ hybridization using a porcine 28S rDNA probe and subsequent visualization of argyrophilic nucleolar proteins by silver staining of extracted and fixed nuclei from in vivo-derived porcine embryos (n = 229). Nucleologenesis was observed by transmission electron microscopy. In general, the 2-cell and 4-cell embryos fixed at 10 and 20 h postcleavage (hpc) showed no signs of rRNA transcription. Four small clusters of fluorescein isothiocyanate (FITC) labeling were visible in interphase nuclei, consistent with hybridization to the rRNA gene clusters only; there was no silver staining at the sites of the rRNA genes and nucleolus precursor bodies. From 30 hpc onwards, most 4-cell embryos had medium size to large clusters of FITC-labeled areas colocalized with silver staining of rRNA gene clusters and fibrillogranular nucleoli. These observations indicate that rRNA transcription had been initiated. These signs of rRNA synthesis could be blocked by actinomycin D, which is a strong inhibitor of RNA polymerase I. The rRNA transcription of porcine embryos is initiated between 20 and 30 hpc, corresponding to the end of the S-phase or the beginning of the G2 phase during the third cell cycle.

First decision: 13 August 2001.

1 This work was supported by the Danish Agricultural and Veterinary Research Council, the Danish Biotechnology Program, and Novo Nordisk A/S.

2 Correspondence and current address: Dorthe Viuff, Department of Molecular Pharmacology, Novo Nordisk A/S, Novo Nordisk Park, 2760 Malov, Denmark. FAX: 45 4443 4587; dviu{at}novonordisk.com




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