Expression of apoptosis related genes in buffalo embryos produced through in vitro fertilization and parthenogenetic activation
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Keywords:
Apoptosis, Buffalo, Embryo, ParthenogenesisAbstract
In present study immature oocytes were obtained from buffalo slaughterhouse ovaries and were subjected to in vitro maturation (IVM) in TCM-199 + 10% FBS + 5 µg/ml pFSH + 0.81 mM sodium pyruvate + 5% buffalo follicular fluid for 24 h in a CO2 incubator (5% CO2, 90–95% relative humidity) at 38.5°C. The maturer oocytes were used for IVF and the cleaved embryos were cultured for 8 days, while the parthenotes were produced with exposure of 7% ethanol, 6- dimethyl aminopurine and cultured for 8 days in mCR2aa medium. The relative abundance of BCL-XL transcripts in immature, matured oocytes; and embryos produced through IVF i.e. 2-cell, 4-cell, 8-16-cell, morula and blastocyst stage were 25.33±0.90, 12.67±1.20, 37.67±0.90, 30.67±0.30, 23.67±0.90, 18.33±0.90 and 27.00±1.20 respectively, while in parthenogenesis these values were 23.67±0.88, 13.67±1.20, 23.67±1.20, 22.34±0.88, 24.34±0.88, 33.67±0.88, 45.34±1.20 respectively. Relative abundance of BAX transcripts by IVF were 23.0±0.60, 0.33±0.10, 4.00±0.60, 5.00±0.60, 0.37±0.06, 13.0±0.66 and 56.7±0.90; and by parthenonenesis were 22.3±0.90, 0.13±0.03, 13.67±0.90, 14.0±0.60, 15.33±0.90, 64.67±2.20 and 55.0±2.10 respectively. In conclusion, expression pattern of apoptosis related genes revealed that incidence of apoptosis was significantly higher in IVF and parthenogenetically produced buffalo embryos at stages like immature oocytes, morula and blastocyst stage than the early cleavage stage embryos.
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References
Barnes F L and First N L. 1991. Embryonic transcription in in vitro cultured bovine embryos. Molecular Reproduction and Development 29: 117–23.
Beatty R A. 1967. Parthenogenesis in vertebrates. Fertilization. (Eds) Metz C B and Monroy A. Pp. 413–40. New York and London Academic Press.
Betts D H and King W A. 2001. Genetic regulation of embryo death and senescence. Theriogenology 55:171–91.
Byrne A T, Sothgate J, Brison D R and Leese H J. 1999. Analysis of apoptosis in the preimplantation bovine embryo using TUNEL. Journal of Reproduction and Fertility 117: 97–105.
Chauhan M S, Singla S K, Manik R S and Madan M L. 1997. Increased capacitation of buffalo sperm by heparin as confirmed by electron microscopy and in vitro fertilization. Indian Journal of Experimental Biology 35: 1038–43.
Elamaran G, Singh K P, Singh M K, Singla S K, Chauhan M S, Manik R S and Palta P. 2012. Oxygen concentration and cysteamine supplementation during in vitro production of buffalo (Bubalus bubalis) embryos affect mRNA expression of BCL-2, BCL-XL, MCL–1, BAX and BID. Reproduction in Domestic Animals 47(6): 1027–36.
Gasparrini B, Boccia L, Rosa A D, Palo R D, Campanile G and Zicarelli L. 2004. Chemical activation of buffalo (Bubalus bubalis) oocytes by different methods: effects of aging on post- parthenogenetic development. Theriogenology 62: 1627–37.
Gasparrini B. 2002. In vitro embryo production in buffalo species: state of ART. Theriogenology 57: 237–56.
Gjorret J O, Knijn H M, Dieleman S J, Avery B, Larsson L I and Maddox Hyttel P. 2003. Chronology of apoptosis in bovine embryos produced in vivo and in vitro. Biology of Reproduction 69: 1193–200.
Hao Y, Lai L, Mao J, Im G, Bonk A and Prather R S. 2004. Apoptosis in parthenogenetic preimplantation porcine embryos. Biology of Reproduction 70: 1644–49.
Hardy K, Handyside A H and Winston R M. 1989. The human blastocyst: cell number, death and allocation during late preimplantation development in vitro. Development 107: 597– 604.
Hardy K. 1997. Cell death in the mammalian blastocyst. Molecular Human Reproduction 3: 919–25.
Jurisicova A, Latham E, Casper R F and Varmuza S L. 1998. Expression and regulation of genes associated with cell death during murine preimplantation embryo development. Molecular Reproduction and development 51: 243–53.
Kastan M B, Oneykwere O, Sidransky D, Vogelstein B and Craig R W. 1991. Participation of p53 protein in the cellular response to DNA damage. Cancer Research 51: 6304–11.
Krajewski S, Tanaka S, Takayama S, Schibler M J, Fenton W and Reed J C. 1993. Investigation of the subcellular distribution of the bcl–2 oncoprotein: residence in the nuclear envelope, endoplasmic reticulum, and outer mitochondrial membranes. Cancer Research 53(19): 4701–14.
Kumar D, Anand T, Shah R A, Singh M K, Chauhan M S and Manik R S. 2012. Expression patterns of OCT-4 and NANOG genes in buffalo (Bubalus bubalis) embryos produced by in vitro fertilization or parthenogenetic activation. Indian Journal of Animal Sciences 82 (8): 834–37.
Liu L, Ju J C and Yang X. 1998. Parthenogenetic development and protein patterns of newly matured bovine oocytes following chemical activation. Molecular Reproduction and Development 49: 298–307.
Lonergan P, Rizos D, Kanka J, Nemcova L, Mbaye A M, Kingston M, Wade M, Duffy P and Boland M P. 2003. Temporal sensitivity of bovine embryos to culture environment after fertilization and the implications for blastocyst quality. Reproduction 126: 337– 46.
Oltvai Z N, Milliman C L and Korsmeyer S J. 1993. Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death. Cell 74: 609–19.
Ongeri E M, Bormann C L, Butler R E, Melican D, Gavin W G, Echelard Y and Krisher Behboodi E. 2001. Development of goat embryo after in vitro fertilization and parthenogenetic activation by different methods. Theriogenology 55: 1933–45.
Palta P and Chauhan M S. 1998. Laboratory production of buffalo (Bubalus bubalis) embryos. Reproduction Fertility and Development 10: 379–91.
Rich T, Watson C J and Wyllie A. 1999. Apoptosis: the germs of death. Nature Cell Biology 1: E69–71.
Singh K P, Kaushik R, Garg V, Sharma R, George A, Singh M K, Manik R S, Palta P, Singla S K and Chauhan M S. 2012. Expression pattern of pluripotent markers in different embryonic developmental stages of buffalo (Bubalus bubalis) embryos and putative embryonic stem cells generated by parthenogenetic activation. Cellular Reprogramming 14(6): 530–38.
Wyllie A H. 1995. The genetic regulation of apoptosis. Current Opinion in Genetics and Development 5: 97–104.
Yang E, Zha J, Jackel J, Boise L H, Thompson C B and Korsmeyer S J. 1995. Bad, a heterodimeric partner for bcl-xl and bcl-2 displaces bax and promotes cell death. Cell 80: 285–91.
Yang M Y and Rajamahendran R. 2002. Expression of Bcl-2 and Bax proteins in relation to quality of bovine oocytes and embryos produced in vitro. Animal Reproduction Science 70: 159–69.
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