Silencing CENPF in bovine preimplantation embryo induces arrest at 8-cell stage
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19651849
DOI
10.1530/rep-09-0234
PII: REP-09-0234
Knihovny.cz E-resources
- MeSH
- Blastocyst cytology metabolism physiology MeSH
- Cell Division genetics physiology MeSH
- Chromosomal Proteins, Non-Histone antagonists & inhibitors genetics metabolism MeSH
- Embryonic Development genetics physiology MeSH
- Fertilization in Vitro veterinary MeSH
- Cell Cycle Checkpoints genetics physiology MeSH
- Cells, Cultured MeSH
- Microfilament Proteins antagonists & inhibitors genetics metabolism MeSH
- Cattle * embryology genetics physiology MeSH
- Cleavage Stage, Ovum metabolism physiology MeSH
- Gene Silencing physiology MeSH
- Gene Expression Regulation, Developmental MeSH
- Animals MeSH
- Check Tag
- Cattle * embryology genetics physiology MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- centromere protein F MeSH Browser
- Chromosomal Proteins, Non-Histone MeSH
- Microfilament Proteins MeSH
Identification of genes that are important for normal preimplantation development is essential for understanding the basics of early mammalian embryogenesis. In our previous study, we have shown that CENPF (mitosin) is differentially expressed during preimplantation development of bovine embryos. CENPF is a centromere-kinetochore complex protein that plays a crucial role in the cell division of somatic cells. To our best knowledge, no study has yet been done on either bovine model, or oocytes and preimplantation embryos. In this study, we focused on the fate of bovine embryos after injection of CENPF double-stranded RNA (dsRNA) into the zygotes. An average decrease of CENPF mRNA abundance by 94.9% or more and an extensive decline in immunofluorescence staining intensity was detected relative to controls. There was no disparity between individual groups in the developmental competence before the 8-cell stage. However, the developmental competence rapidly decreased then and only 28.1% of CENPF dsRNA injected 8-cell embryos were able to develop further (uninjected control: 71.8%; green fluorescent protein dsRNA injected control: 72.0%). In conclusion, these results show that depletion of CENPF mRNA in preimplantation bovine embryos leads to dramatic decrease of developmental competence after embryonic genome activation.
References provided by Crossref.org
The neglected part of early embryonic development: maternal protein degradation
Characterization of SCF-Complex during Bovine Preimplantation Development