Efficient transgene expression in IVF and parthenogenetic bovine embryos by intracytoplasmic injection of DNA - liposome complexes
Transgenic animals constitute an important tool with many biotechnological applications. Although there have been advances in this field, we propose a novel method that may greatly increase the efficiency of transgenic animal production and thereby its application. This new technique consists of int...
| Autor principal: | |
|---|---|
| Otros Autores: | , |
| Formato: | Artículo |
| Lenguaje: | Inglés |
| Materias: | |
| Acceso en línea: | http://ri.agro.uba.ar/files/intranet/articulo/2011Vichera.pdf LINK AL EDITOR |
| Aporte de: | Registro referencial: Solicitar el recurso aquí |
| LEADER | 07844nab a22013817a 4500 | ||
|---|---|---|---|
| 001 | AR-BaUFA000222 | ||
| 003 | AR-BaUFA | ||
| 005 | 20220808101657.0 | ||
| 008 | 181208t2011 |||||o|||||00||||eng d | ||
| 999 | |c 46656 |d 46656 | ||
| 022 | |a 0936-6768 | ||
| 024 | |a 10.1111/j.1439-0531.2010.01642.x | ||
| 040 | |a AR-BaUFA |c AR-BaUFA | ||
| 100 | 1 | |9 34779 |a Vichera, Gabriel Damián | |
| 245 | 0 | 0 | |a Efficient transgene expression in IVF and parthenogenetic bovine embryos by intracytoplasmic injection of DNA - liposome complexes |
| 520 | |a Transgenic animals constitute an important tool with many biotechnological applications. Although there have been advances in this field, we propose a novel method that may greatly increase the efficiency of transgenic animal production and thereby its application. This new technique consists of intracytoplasmic injection of liposomes, in bovine oocytes and zygotes, to introduce exogenous DNA. In the first experiment, we evaluated embryo development and EGFP expression in In Vitro Fertilization [IVF] embryos injected with different concentrations of exogenous DNA-liposome complexes [0.5, 5, 50, 500ng pCX-EGFP/ul]. The highest EGFP-embryos rates were obtained using 500ng pCX-EGFP/ul. In the second experiment, we evaluated embryo development and EGFP expression following the injection of DNA-liposome complexes into pre-fertilized oocytes and presumptive zygotes, 16 and 24h post-fertilization. Approximately 70 percent of the cleaved embryos and 50 percent of the blastocysts expressed EGFP, when egfp-liposome was injected 16h post-fertilization. The percentages of positive embryos for the 24-h post-fertilization and pre-fertilization groups were 30.1 and 6.3, respectively. Blastocysts that developed from injected zygotes were analysed by PCR, confirming the presence of transgene in all embryos. Finally, we examined the embryo development and EGFP expression of parthenogenetic embryos that resulted from the injection of egfp-liposome complexes into pre-activated oocytes, and 3 and 11h post-activated oocytes. The group with the highest expression rate [48.4 percent] was the one injected 3h post-activation. In summary, this study reports the efficient, reproducible and fast production of IVF and parthenogenetic embryos expressing EGFP, by the intracytoplasmic injection of liposomes to introduce the foreign DNA. | ||
| 653 | 0 | |a ENHANCED GREEN FLUORESCENT PROTEIN | |
| 653 | 0 | |a GREEN FLUORESCENT PROTEIN | |
| 653 | 0 | |a LIPOSOME | |
| 653 | 0 | |a ANIMAL | |
| 653 | 0 | |a ANIMAL DISEASE | |
| 653 | 0 | |a ANIMAL EMBRYO | |
| 653 | 0 | |a CATTLE | |
| 653 | 0 | |a FEMALE | |
| 653 | 0 | |a FERTILIZATION IN VITRO | |
| 653 | 0 | |a GENE EXPRESSION REGULATION | |
| 653 | 0 | |a GENE TRANSFER | |
| 653 | 0 | |a GENETICS | |
| 653 | 0 | |a METABOLISM | |
| 653 | 0 | |a PARTHENOGENESIS | |
| 653 | 0 | |a PHYSIOLOGY | |
| 653 | 0 | |a TRANSGENIC ANIMAL | |
| 653 | 0 | |a ANIMALS | |
| 653 | 0 | |a ANIMALS, GENETICALLY MODIFIED | |
| 653 | 0 | |a DNA | |
| 653 | 0 | |a EMBRYO, MAMMALIAN | |
| 653 | 0 | |a GENE EXPRESSION REGULATION, DEVELOPMENTAL | |
| 653 | 0 | |a GENE TRANSFER TECHNIQUES | |
| 653 | 0 | |a GREEN FLUORESCENT PROTEINS | |
| 653 | 0 | |a LIPOSOMES | |
| 653 | 0 | |a PARTHENOGENESIS | |
| 653 | 0 | |a ANIMALIA | |
| 653 | 0 | |a BOVINAE | |
| 700 | 1 | |9 47630 |a Moro, L. N. | |
| 700 | 1 | |9 61021 |a Salamone, Daniel Felipe | |
| 773 | |t Reproduction in Domestic Animals |g Vol.46, no.2 (2011), p.214-220 | ||
| 856 | |u http://ri.agro.uba.ar/files/intranet/articulo/2011Vichera.pdf |i En reservorio |q application/pdf |f 2011Vichera |x MIGRADOS2018 | ||
| 856 | |u http://www.wiley.com/ |x MIGRADOS2018 |z LINK AL EDITOR | ||
| 900 | |a as | ||
| 900 | |a 20131220 | ||
| 900 | |a N | ||
| 900 | |a SCOPUS | ||
| 900 | |a a | ||
| 900 | |a s | ||
| 900 | |a ARTICULO | ||
| 900 | |a EN LINEA | ||
| 900 | |a 09366768 | ||
| 900 | |a 10.1111/j.1439-0531.2010.01642.x | ||
| 900 | |a ^tEfficient Transgene Expression in IVF and Parthenogenetic Bovine Embryos by Intracytoplasmic Injection of DNA-Liposome Complexes | ||
| 900 | |a ^aVichera^bG. | ||
| 900 | |a ^aMoro^bL. | ||
| 900 | |a ^aSalamone^bD. | ||
| 900 | |a ^aVichera^bG. | ||
| 900 | |a ^aMoro^bL. N. | ||
| 900 | |a ^aSalamone^bD. F. | ||
| 900 | |a ^aVichera^bG.^tLaboratorio de BiotecnologÃa Animal, Facultad de AgronomÃa, Universidad de Buenos Aires, Buenos Aires, Argentina | ||
| 900 | |a ^aMoro^bL. | ||
| 900 | |a ^aSalamone^bD. | ||
| 900 | |a ^tReproduction in Domestic Animals^cReprod. Domest. Anim. | ||
| 900 | |a en | ||
| 900 | |a 214 | ||
| 900 | |a ^i | ||
| 900 | |a Vol. 46, no. 2 | ||
| 900 | |a 220 | ||
| 900 | |a ENHANCED GREEN FLUORESCENT PROTEIN | ||
| 900 | |a GREEN FLUORESCENT PROTEIN | ||
| 900 | |a LIPOSOME | ||
| 900 | |a ANIMAL | ||
| 900 | |a ANIMAL DISEASE | ||
| 900 | |a ANIMAL EMBRYO | ||
| 900 | |a CATTLE | ||
| 900 | |a FEMALE | ||
| 900 | |a FERTILIZATION IN VITRO | ||
| 900 | |a GENE EXPRESSION REGULATION | ||
| 900 | |a GENE TRANSFER | ||
| 900 | |a GENETICS | ||
| 900 | |a METABOLISM | ||
| 900 | |a PARTHENOGENESIS | ||
| 900 | |a PHYSIOLOGY | ||
| 900 | |a TRANSGENIC ANIMAL | ||
| 900 | |a ANIMALS | ||
| 900 | |a ANIMALS, GENETICALLY MODIFIED | ||
| 900 | |a DNA | ||
| 900 | |a EMBRYO, MAMMALIAN | ||
| 900 | |a GENE EXPRESSION REGULATION, DEVELOPMENTAL | ||
| 900 | |a GENE TRANSFER TECHNIQUES | ||
| 900 | |a GREEN FLUORESCENT PROTEINS | ||
| 900 | |a LIPOSOMES | ||
| 900 | |a PARTHENOGENESIS | ||
| 900 | |a ANIMALIA | ||
| 900 | |a BOVINAE | ||
| 900 | |a Transgenic animals constitute an important tool with many biotechnological applications. Although there have been advances in this field, we propose a novel method that may greatly increase the efficiency of transgenic animal production and thereby its application. This new technique consists of intracytoplasmic injection of liposomes, in bovine oocytes and zygotes, to introduce exogenous DNA. In the first experiment, we evaluated embryo development and EGFP expression in In Vitro Fertilization [IVF] embryos injected with different concentrations of exogenous DNA-liposome complexes [0.5, 5, 50, 500ng pCX-EGFP/ul]. The highest EGFP-embryos rates were obtained using 500ng pCX-EGFP/ul. In the second experiment, we evaluated embryo development and EGFP expression following the injection of DNA-liposome complexes into pre-fertilized oocytes and presumptive zygotes, 16 and 24h post-fertilization. Approximately 70 percent of the cleaved embryos and 50 percent of the blastocysts expressed EGFP, when egfp-liposome was injected 16h post-fertilization. The percentages of positive embryos for the 24-h post-fertilization and pre-fertilization groups were 30.1 and 6.3, respectively. Blastocysts that developed from injected zygotes were analysed by PCR, confirming the presence of transgene in all embryos. Finally, we examined the embryo development and EGFP expression of parthenogenetic embryos that resulted from the injection of egfp-liposome complexes into pre-activated oocytes, and 3 and 11h post-activated oocytes. The group with the highest expression rate [48.4 percent] was the one injected 3h post-activation. In summary, this study reports the efficient, reproducible and fast production of IVF and parthenogenetic embryos expressing EGFP, by the intracytoplasmic injection of liposomes to introduce the foreign DNA. | ||
| 900 | |a 46 | ||
| 900 | |a 2 | ||
| 900 | |a 2011 | ||
| 900 | |a ^cH | ||
| 900 | |a AAG | ||
| 900 | |a AGROVOC | ||
| 900 | |a 2011Vichera | ||
| 900 | |a AAG | ||
| 900 | |a http://ri.agro.uba.ar/files/intranet/articulo/2011Vichera.pdf | ||
| 900 | |a 2011Vichera.pdf | ||
| 900 | |a http://www.wiley.com/ | ||
| 900 | |a http://www.scopus.com/inward/record.url?eid=2-s2.0-79952607999&partnerID=40&md5=4aa85f5243d423939cd9fab98a62ce98 | ||
| 900 | |a ^a^b^c^d^e^f^g^h^i | ||
| 900 | |a OS | ||
| 942 | 0 | 0 | |c ARTICULO |2 udc |
| 942 | 0 | 0 | |c ENLINEA |2 udc |