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Vertebrate reproductive science and technology
RESEARCH ARTICLE

Depletion of BIRC6 leads to retarded bovine early embryonic development and blastocyst formation in vitro

Dessie Salilew-Wondim A , Micheal Hölker A , Franca Rings A , Chirawath Phatsara A , Abdollah Mohammadi-Sangcheshmeh A , Ernst Tholen A , Karl Schellander A and Dawit Tesfaye A B
+ Author Affiliations
- Author Affiliations

A Institute of Animal Science, Animal Breeding and Husbandry Group, University of Bonn, Endenicher Allee 15, Bonn, Germany.

B Corresponding author. Email: tesfaye@itz.uni-bonn.de

Reproduction, Fertility and Development 22(3) 564-579 https://doi.org/10.1071/RD09112
Submitted: 1 May 2009  Accepted: 16 September 2009   Published: 23 February 2010

Abstract

Baculoviral inhibitors of apoptosis repeat-containing 6 (BIRC6) is believed to inhibit apoptosis by targeting key cell-death proteins. To understand its involvement during bovine preimplantation embryo development, two consecutive experiments were conducted by targeted knockdown of its mRNA and protein using RNA interference. In Experiment 1, the effect of BIRC6 knockdown during the early stages of preimplantation embryo development was assessed by injecting zygotes with long double-stranded RNA (ldsRNA) and short hairpin RNA (shRNA) against BIRC6 mRNA followed by in vitro culturing until 96 h post insemination (hpi). The results showed that in RNA-injected zygote groups, reduced levels of BIRC6 mRNA and protein were accompanied by an increase (P < 0.05) in the proportion of 2- and 4-cell and uncleaved embryos and a corresponding decrease (P < 0.05) in the number of 8-cell embryos. In Experiment 2, the effect of BIRC6 knockdown on blastocyst formation, blastocyst total cell number and the extent of apoptosis was investigated. Consequently, zygotes injected with ldsRNA and shRNA resulted in lower (P < 0.05) blastocyst formation and total blastocyst cell number. Moreover, the apoptotic cell ratio, CASPASE 3 and 7 activity, BAX to BCL-2 ratio and levels of SMAC and CASPASE 9 were higher in blastocysts derived from the ldsRNA and shRNA groups, suggesting increased apoptosis in those blastocysts. The results of this study reveal the importance of BIRC6 expression for embryo survival during bovine preimplantation embryo development. However, whether BIRC6 is essential for implantation and fetal development during bovine pregnancy needs further research.

Additional keywords: apoptosis, RNA interference.


References

Alikani, M. , Cohen, J. , Tomkin, G. , Garrisi, G. J. , Mack, C. , and Scott, R. T. (1999). Human embryo fragmentation in vitro and its implications for pregnancy and implantation. Fertil. Steril. 71, 836–842.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Amanai, M. , Shoji, S. , Yoshida, N. , Brahmajosyula, M. , and Perry, A. (2006). Injection of mammalian metaphase II oocytes with short interfering RNAs to dissect meiotic and early mitotic events. Biol. Reprod. 75, 891–898.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Antunes, G. , Chaveiro, A. , Santos, P. , Marques, A. , Jin, H. S. , and Moreira da Silva, F. (2008). Influence of apoptosis in bovine embryo’s development. Reprod. Domest. Anim. ,
Crossref | GoogleScholarGoogle Scholar |

Arama, E. , Agapite, J. , and Steller, H. (2003). Caspase activity and a specific cytochrome C are required for sperm differentiation in Drosophila. Dev. Cell 4, 687–697.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Bartke, T. , Pohl, C. , Pyrowolakis, G. , and Jentsch, S. (2004). Dual role of BRUCE as an antiapoptotic IAP and a chimeric E2/E3 ubiquitin ligase. Mol. Cell 14, 801–811.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Bianchini, M. , Levy, E. , Zucchini, C. , Pinski, V. , Macagno, C. , De Sanctis, P. , Valvassori, L. , Carinci, P. , and Mordoh, J. (2006). Comparative study of gene expression by cDNA microarray in human colorectal cancer tissues and normal mucosa. Int. J. Oncol. 29, 83–94.
PubMed |  CAS |

Bustin, S. A. , Benes, V. , Garson, J. A. , Hellemans, J. , and Huggett, J. , et al. (2009). The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin. Chem. 55, 611–622.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Cabot, R. A. , and Prather, R. (2003). Cleavage stage porcine embryos may have differing developmental requirements for karyopherins alpha2 and alpha3. Mol. Reprod. Dev. 64, 292–301.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Chao, D. T. , and Korsmeyer, S. J. (1998). BCL-2 family: regulators of cell death. Annu. Rev. Immunol. 16, 395–419.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Chen, Z. , Naito, M. , Hori, S. , Mashima, T. , Yamori, T. , and Tsuruo, T. (1999). A human IAP-family gene, apollon, expressed in human brain cancer cells. Biochem. Biophys. Res. Commun. 264, 847–854.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Chu, L. , Gu, J. , Sun, L. , Qian, Q. , Qian, C. , and Liu, X. (2008). Oncolytic adenovirus-mediated shRNA against Apollon inhibits tumor cell growth and enhances antitumor effect of 5-fluorouracil. Gene Ther. 15, 484–494.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Corteling, R. L. , Brett, S. E. , Yin, H. , Zheng, X. L. , Walsh, M. P. , and Welsh, D. J. (2007). The functional consequence of RhoA knockdown by RNA interference in rat cerebral arteries. Am. J. Physiol. Heart Circ. Physiol. 293, H440–H447.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Deveraux, Q. L. , and Reed, J. C. (1999). IAP family proteins suppressors of apoptosis. Genes Dev. 13, 239–252.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

El-Sayed, A. , Hoelker, M. , Rings, F. , Salilew, D. , Jennen, D. , Tholen, E. , Sirard, M. A. , Schellander, K. , and Tesfaye, D. (2006). Large-scale transcriptional analysis of bovine embryo biopsies in relation to pregnancy success after transfer to recipients. Physiol. Genomics 28, 84–96.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Exley, G. E. , Tang, C. , McElhinny, A. S. , and Warner, C. (1999). Expression of caspase and BCL-2 apoptotic family members in mouse preimplantation embryos. Biol. Reprod. 61, 231–239.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Fire, A. , Xu, S. , Montgomery, M. K. , Kostas, S. A. , Driver, S. E. , and Mello, C. (1998). Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 391, 806–811.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Gjørret, J. O. , Fabian, D. , Avery, B. , and Maddox-Hyttel, P. (2007). Active caspase-3 and ultrastructural evidence of apoptosis in spontaneous and induced cell death in bovine in vitro-produced pre-implantation embryos. Mol. Reprod. Dev. 74, 961–971.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Golding, M. C. , Long, C. R. , Carmell, M. A. , Hannon, G. J. , and Westhusin, M. (2006). Suppression of prion protein in livestock by RNA interference. Proc. Natl. Acad. Sci. USA 103, 5285–5290.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Groc, L. , Bezin, L. , Jiang, H. , Jackson, T. S. , and Levine, R. A. (2001). Bax, Bcl-2, and cyclin expression and apoptosis in rat substantia nigra during development. Neurosci. Lett. 306, 198–202.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Gutiérrez-Adán, A. , Rizos, D. , Fair, T. , Moreira, P. N. , Pintado, B. , de la Fuente, J. , Boland, M. P. , and Lonergan, P. (2004). Effect of speed of development on mRNA expression pattern in early bovine embryos cultured in vivo or in vitro. Mol. Reprod. Dev. 68, 441–448.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Hao, Y. , Sekine, K. , Kawabata, A. , Nakamura, H. , and Ishioka, T. , et al. (2004). Apollon ubiquitinates SMAC and caspase-9 and has an essential cytoprotection function. Nat. Cell Biol. 6, 849–860.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Hitz, C. , Vogt-Weisenhorn, D. , Ruiz, P. , Wurst, W. , and Floss, T. (2005). Progressive loss of the spongiotrophoblast layer of BIRC6/Bruce mutants results in embryonic lethality. Genesis 42, 91–103.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Jarskog, L. F. , Selinger, E. S. , Lieberman, J. A. , and Gilmore, J. H. (2004). Apoptotic proteins in the temporal cortex in schizophrenia: high Bax/Bcl-2 ratio without caspase-3 activation. Am. J. Psychiatry 161, 109–115.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Kennerdell, J. R. , and Carthew, R. W. (2000). Heritable gene silencing in Drosophila using double-stranded RNA. Nat. Biotechnol. 18, 896–898.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Kluck, R. M. , Bossy-Wetzel, E. , Green, D. R. , and Newmeyer, D. D. (1997). The release of cytochrome c from mitochondria: a primary site for Bcl-2 regulation of apoptosis. Science 275, 1132–1136.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Lequarre, A. S. , Traverso, J. M. , Marchandise, J. , and Donnay, I. (2004). Poly(A) RNA is reduced by half during bovine oocyte maturation but increases when meiotic arrest is maintained with CDK inhibitors. Biol. Reprod. 71, 425–431.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Lonergan, P. , Rizos, D. , Gutierrez-Adán, A. , Moreira, P. M. , Pintado, B. , de la Fuente, J. , and Boland, M. P. (2003). Temporal divergence in the pattern of messenger RNA expression in bovine embryos cultured from the zygote to blastocyst stage in vitro or in vivo. Biol. Reprod. 69, 1424–1431.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Lopergolo, A. , Pennati, M. , Gandellini, P. , Orlotti, N. I. , Poma, P. , Daidone, M.G. , Folini, M. , and Zaffaroni, N. (2009). Apollon gene silencing induces apoptosis in breast cancer cells through p53 stabilisation and caspase-3 activation. Br. J. Cancer 100, 739–746.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Lotz, K. , Pyrowolakis, G. , and Jentsch, S. (2004). BRUCE, a giant E2/E3 ubiquitin ligase and inhibitor of apoptosis protein of the trans-Golgi network, is required for normal placenta development and mouse survival. Mol. Cell. Biol. 24, 9339–9350.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Makarevich, A. V. , and Markkula, M. (2002). Apoptosis and cell proliferation potential of bovine embryos stimulated with insulin-like growth factor I during in vitro maturation and culture. Biol. Reprod. 66, 386–392.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Nganvongpanit, K. , Müller, H. , Rings, F. , Gilles, M. , Jennen, D. , Hölker, M. , Tholen, E. , Schellander, K. , and Tesfaye, D. (2006a). Targeted suppression of E-cadherin gene expression in bovine preimplantation embryo by RNA interference technology using double-stranded RNA. Mol. Reprod. Dev. 73, 153–163.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Nganvongpanit, K. , Müller, H. , Rings, F. , Hoelker, M. , Jennen, D. , Tholen, E. , Havlicek, V. , Besenfelder, U. , Schellander, K. , and Tesfaye, D. (2006b). Selective degradation of maternal and embryonic transcripts in in vitro produced bovine oocytes and embryos using sequence-specific double-stranded RNA. Reproduction 131, 861–874.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Oltval, 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, 609–619.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Paddison, P. J. , Caudy, A. A. , Bernstein, E. , Hannon, G. J. , and Conklin, D. S. (2002). Short hairpin RNAs (shRNAs) induce sequence-specific silencing in mammalian cells. Genes Dev. 16, 948–958.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Paradis, F. , Vigneault, C. , Robert, C. , and Sirard, M. (2005). RNA interference as a tool to study gene function in bovine oocytes. Mol. Reprod. Dev. 70, 111–121.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Park, S. Y. , Kim, E. Y. , Cui, X. S. , Tae, J. C. , Lee, W. D. , Kim, N. H. , Park, S. P. , and Lim, J. H. (2006). Increase in DNA fragmentation and apoptosis-related gene expression in frozen–thawed bovine blastocysts. Zygote 14, 125–131.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Park, S. Y. , Kim, E. Y. , Jeon, K. , Cui, X. S. , Lee, W. D. , Kim, N. H. , Park, S. P. , and Lim, J. (2007). Survivin acts as anti-apoptotic factor during the development of bovine pre-implantation embryos. Mol. Reprod. Dev. 74, 582–590.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Qiu, X. B. , and Goldberg, A. (2005). The membrane-associated inhibitor of apoptosis protein, BRUCE/Apollon, antagonizes both the precursor and mature forms of Smac and caspase-9. J. Biol. Chem. 280, 174–182.
PubMed |  CAS |

Qiu, X. B. , Markant, S. L. , Yuan, J. , and Goldberg, A. (2004). Nrdp1-mediated degradation of the gigantic IAP, BRUCE, is a novel pathway for triggering apoptosis. EMBO J. 23, 800–810.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Reed, J. C. (1997). Double identity for proteins of the Bcl-2 family. Nature 387, 773–776.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Ren, J. , Shi, M. , Liu, R. , Yang, Q. H. , Johnson, T. , Skarnes, W. C. , and Du, C. (2005). The Birc6 (Bruce) gene regulates p53 and the mitochondrial pathway of apoptosis and is essential for mouse embryonic development. Proc. Natl. Acad. Sci. USA 102, 565–570.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Roccheri, M. C. , Tipa, C. , Bonaventura, R. , and Matranga, V. (2002). Physiological and induced apoptosis in sea urchin larvae undergoing metamorphosis. Int. J. Dev. Biol. 46, 801–806.
PubMed |

Salilew-Wondim, D. , Rings, F. , Hölker, M. , Gilles, M. , and Jennen, D. , et al. (2007). Dielectrophoretic behaviour of in vitro-derived bovine metaphase II oocytes and zygotes and its relation to in vitro embryonic developmental competence and mRNA expression pattern. Reproduction 133, 931–946.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Salvesen, G. , and Duckett, C. S. (2002). IAP proteins: blocking the road to death’s door. Nat. Rev. Mol. Cell Biol. 3, 401–410.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Sato, F. , Kurokawa, M. , Yamauchi, N. , and Hattori, M. A. (2006). Gene silencing of myostatin in differentiation of chicken embryonic myoblasts by small interfering RNA. Am. J. Physiol. Cell Physiol. 291, C538–C545.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Soares, M. L. , Haraguchi, S. , Torres-Padilla, M. E. , Kalmar, T. , and Carpenter, L. , et al. (2005). Functional studies of signalling pathways in peri-implantation development of the mouse embryo by RNAi. BMC Dev. Biol. 5, 28.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Telford, N. A. , Watson, A. J. , and Schultz, G. A. (1990). Transition from maternal to embryonic control in early mammalian development: a comparison of several species. Mol. Reprod. Dev. 26, 90–100.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Tesfaye, D. , Wimmers, K. , Gilles, M. , and Schellander, K. (2004). A comparative expression analysis of gene transcripts in post-fertilization developmental stages of bovine embryos produced in vitro or in vivo. Reprod. Domest. Anim. 39, 396–404.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Tesfaye, D. , Lonergan, P. , Hoelker, M. , Rings, F. , Nganvongpanit, K. , Havlicek, V. , Besenfelder, U. , Jennen, D. , Tholen, E. , and Schellander, K. (2007). Suppression of connexin 43 and E-cadherin transcripts in in vitro-derived bovine embryos following culture in vitro or in vivo in the homologous bovine oviduct. Mol. Reprod. Dev. 74, 978–988.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Thélie, A. , Pennetier, S. , Perreau, C. , Traverso, J. M. , Uzbekova, S. , Mermillod, P. , Joly, C. , Humblot, P. , and Dalbiès-Tran, R. (2007). Differential regulation of abundance and deadenylation of maternal transcripts during bovine oocyte maturation in vitro and in vivo. BMC Dev. Biol. 7, 125.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Vandaele, L. , Maes, D. , de Kruif, A. , and Van Soom, A. (2006). Is apoptosis in bovine in vitro-produced embryos related to early developmental kinetics and in vivo bull fertility? Theriogenology 65, 1691–1703.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Verhagen, A. M. , Coulson, E. J. , and Vaux, D. L. (2001). Inhibitor of apoptosis proteins and their relatives: IAPs and other BIRPs. Genome Biol. 2, reviews3009.1–reviews3009.10.
Crossref | GoogleScholarGoogle Scholar |

Warner, C. M. , McElhinny, A. S. , and Tang, C. (1998). Genetic regulation of preimplantation mouse embryo survival. J. Exp. Zool. 282, 272–279.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Wianny, F. , and Zernicka-Goetz, M. (2000). Specific interference with gene function by double-stranded RNA in early mouse development. Nat. Cell Biol. 2, 70–75.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Wieschaus, E. (1996). Embryonic transcription and the control of developmental pathways. Genetics 142, 5–10.
PubMed |  CAS |

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. Anim. Reprod. Sci. 70, 159–169.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |