Biology of Reproduction · 2000 · 251 citations · 24 references
Life SciencesDevelopmental BiologyMolecular BiologyEmbryo TransferEmbryologyGene ExpressionBlastocyst DevelopmentEarly Embryonic DevelopmentEmbryo ImplantationMammalian EmbryologyPreimplantation Embryo DevelopmentSomatic Cell Nuclear TransferCell ReprogrammingDonor Nucleus TransferEarly Embryo DevelopmentGene-specific Transcription FactorsNuclear Transfer EmbryologyNuclear Transfer TechniquesReprogramming Of Somatic Cells
The low efficiency of animal production using somatic cell nuclear transfer procedures is considered to be the result of an incomplete reprogramming of the donor somatic cell nucleus, which leads to a lack of, or abnormal expression of developmentally important genes. However, our current understanding of the process of somatic cell nuclear reprogramming and its effect on gene expression is limited. In this study, we compare the transcription patterns of six developmentally important genes, Oct4, IL6, FGF2, FGF4, FGFr2, and gp130 in single in vitro fertilized (IVF) and nuclear transfer embryos reconstructed using granulosa cells for the donor nuclei. Similar patterns of transcription were detected for Oct4, FGF2, and gp130 in IVF and nuclear transfer embryos during the preimplantation stages of development. However, a number of morula- and blastocyst-stage embryos derived from nuclear transfer procedures showed abnormal transcription of IL6, FGF4, and FGFr2. Previous studies have demonstrated that these three genes play an important role in implantation, early postimplantation development, or both in the mouse. Therefore, the aberrant transcription patterns detected in nuclear transfer embryos may lead to a reduction in embryo viability.
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Viable offspring derived from fetal and adult mammalian cells
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