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Reproduction (2008) 136 777-785
DOI: 10.1530/REP-08-0045
Copyright © 2008 Society for Reproduction and Fertility
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RESEARCH

Polycomb gene expression and histone H3 lysine 27 trimethylation changes during bovine preimplantation development

Pablo J Ross1, Neli P Ragina1, Ramon M Rodriguez1, Amy E Iager1, Kannika Siripattarapravat1, Nestor Lopez-Corrales3 and Jose B Cibelli1,2,4

Departments of1 , Animal Science2 Physiology, Michigan State University, East Lansing, Michigan 48824, USA3 Animal Production Unit, Department of Agriculture, Public University of Navarra, Pamplona, Navarra 31006, Spain4 Programa Andaluz de Terapia Celular y Medicina Regenerativa, Andalucía, Spain

Correspondence should be addressed to J B Cibelli; Email: cibelli{at}msu.edu

Trimethylation of histone H3 at lysine 27 (H3K27me3) is established by polycomb group genes and is associated with stable and heritable gene silencing. The aim of this study was to characterize the expression of polycomb genes and the dynamics of H3K27me3 during bovine oocyte maturation and preimplantation development. Oocytes and in vitro-produced embryos were collected at different stages of development. Polycomb gene expression was analyzed by real-time quantitative RT-PCR and immunofluorescence. Global H3K27me3 levels were determined by semiquantitative immunofluorescence. Transcripts for EZH2, EED, and SUZ12 were detected at all stages analyzed, with EZH2 levels being the highest of the three at early stages of development. By the time the embryo reached the blastocyst stage, the level of PcG gene mRNA levels significantly increased. Immunofluorescence staining indicated nuclear expression of EZH2 at all stages while nuclear localized EED and SUZ12 were only evident at the morula and blastocyst stages. Semiquantitative analysis of H3K27me3 levels showed that nuclear fluorescence intensity was the highest in immature oocytes, which steadily decreased after fertilization to reach a nadir at the eight-cell stage, and then increased at the blastocyst stage. These results suggest that the absence of polycomb repressive complex 2 proteins localized to the nucleus of early embryos could be responsible for the gradual decrease in H3K27me3 during early preimplantation development.




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