Cellular Reprogramming · 2020 · 12 citations · 53 references
Veterinary MedicineDevelopmental BiologyAssisted Reproductive TechnologiesEmbryo TransferIn Vitro FertilizationAnimal CloningEmbryo BiotechnologyEmbryo Transfer TechniquesFertilization TechniquesOocyte MaturationSwine ReproductionCloned Embryo DevelopmentEmbryo Transfer In PigsFollicular Fluid CompositionFollicular Fluid EffectsIn Vitro MaturationOocyte In Vitro FertilizationOocyte Quality MarkersPorcine Cloning
Pig cloning technique is valuable in agriculture, biomedicine, and life sciences. However, the full-term developmental efficiency of cloned pig embryos is only about 1%, which limits pig cloning application. The quality of recipient oocytes greatly affects the developmental competence of cloned pig embryos. Thus, this study investigated the effects of a recipient oocyte source (in vivo matured [IVVM] oocytes vs. slaughter house-derived in vitro matured [IVTM] oocytes), and follicular liquid treatment (slaughter house-derived immature follicle-derived fluid [IFF] vs. in vivo-matured follicle-derived fluid [MFF]) during the in vitro maturation (IVM) of oocytes on the development of the cloned pig embryos. Our results showed that using IVVM oocytes to replace IVTM oocytes as recipient oocytes, and using 10% MFF IVM medium to replace 10% IFF IVM medium could enhance the development of the cloned pig embryos. IFF and MFF contained different levels of oocyte quality-related proteins, resulting in different oocyte quality-related gene expression levels and reactive oxygen species levels between the 10% MFF medium-cultured oocytes and 10% IFF medium-cultured oocytes. This study provided useful information for enhancing the pig cloning efficiency by improving the quality of recipient oocytes.
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Targeted disruption of the α1,3-galactosyltransferase gene in cloned pigs
Yifan Dai, Todd Vaught, Jeremy Boone et al. · Nature Biotechnology · 2002 · 710 citations
Sen Yan, Zhuchi Tu, Zhaoming Liu et al. · Cell · 2018 · 339 citations