Improved functional oocyte enucleation by actinomycin D for bovine somatic cell nuclear transfer
Marcelo T. Moura A B C E , Jeferson Badaraco A , Regivaldo V. Sousa A , Carolina M. Lucci B and Rodolfo Rumpf A B DA Laboratório de Reprodução Animal, Embrapa Recursos Genéticos e Biotecnologia, Parque Estação Biológica, Av. W5 Norte (final), CP 02372, CEP 70770-900, Brasília, DF, Brazil.
B Departamento de Agronomia e Medicina Veterinária, Universidade de Brasília, Instituto Central de Ciências Sul, Campus Universitário Darci Ribeiro, CEP 70297-400, Brasília, DF, Brazil.
C Present address: Laboratório de Biologia Celular, Universidade Federal de São Paulo, Campus Diadema, CEP 09972-270, Diadema, SP, Brazil.
D Present address: Geneal Biotecnologia, Rodovia BR-050, Km 184, CEP 38038-050, Uberaba, MG, Brazil.
E Corresponding author. Email: marcelotmoura@gmail.com
Reproduction, Fertility and Development 31(8) 1321-1329 https://doi.org/10.1071/RD18164
Submitted: 4 May 2018 Accepted: 5 February 2019 Published: 16 April 2019
Abstract
Somatic cell nuclear transfer (SCNT) allows animal cloning but remains technically challenging. This study investigated limitations to functional oocyte enucleation by actinomycin D (AD) as a means of making SCNT easier to perform. Denuding oocytes or inhibiting transcription before AD treatment revealed that the toxicity of this compound during bovine oocyte maturation is mediated by cumulus cells. Exposure of denuded oocytes to higher concentrations of AD (5–20 μg mL−1) and stepwise reductions of the incubation period (from 14.0 to 0.25 h) led to complete inhibition of parthenogenetic development. Bovine SCNT using this improved AD enucleation protocol (NT(AD)) restored cleavage rates compared with rates in the parthenogenetic and SCNT controls (P(CTL) and NT(CTL) respectively). However, NT(AD) was associated with increased caspase-3 activity in cleavage stage embryos and did not recover blastocyst rates. The removal of AD-treated oocyte spindle before reconstruction (NT(AD+SR)) improved embryo development and reduced caspase-3 activity to levels similar to those in the P(CTL) and NT(CTL) groups. Furthermore, mid-term pregnancies were achieved using NT(AD+SR) blastocysts. In conclusion, improvements in AD functional enucleation for bovine SCNT circumvents most cellular roadblocks to early embryonic development and future investigations must focus on restoring blastocyst formation.
Additional keywords: cattle, cytoplast, nuclear transplantation, reprogramming.
References
Akshey, Y. S., Malakar, D., De, A. K., Jena, M. K., Sahu, S., and Dutta, R. (2011). Study of the efficiency of chemically assisted enucleation method for handmade cloning in goat (Capra hircus). Reprod. Domest. Anim. 46, 699–704.| Study of the efficiency of chemically assisted enucleation method for handmade cloning in goat (Capra hircus).Crossref | GoogleScholarGoogle Scholar | 21134007PubMed |
Andreu-Vieyra, C., Lin, Y. N., and Matzuk, M. M. (2006). Mining the oocyte transcriptome. Trends Endocrinol. Metab. 17, 136–143.
| Mining the oocyte transcriptome.Crossref | GoogleScholarGoogle Scholar | 16595178PubMed |
Bayona-Bafaluy, M. P., Manfredi, G., and Moraes, C. T. (2003). A chemical enucleation method for the transfer of mitochondrial DNA to rho(o) cells. Nucleic Acids Res. 31, e98.
| A chemical enucleation method for the transfer of mitochondrial DNA to rho(o) cells.Crossref | GoogleScholarGoogle Scholar | 12954771PubMed |
Bolcun-Filas, E., Rinaldi, V. D., White, M. E., and Schimenti, J. C. (2014). Reversal of female infertility by Chk2 ablation reveals the oocyte DNA damage checkpoint pathway. Science 343, 533–536.
| Reversal of female infertility by Chk2 ablation reveals the oocyte DNA damage checkpoint pathway.Crossref | GoogleScholarGoogle Scholar | 24482479PubMed |
Bradshaw, J., Jung, T., Fulka, J., and Moor, R. M. (1995). UV irradiation of chromosomal DNA and its effects upon MPF and meiosis in mammalian oocytes. Mol. Reprod. Dev. 41, 503–512.
| UV irradiation of chromosomal DNA and its effects upon MPF and meiosis in mammalian oocytes.Crossref | GoogleScholarGoogle Scholar | 7576618PubMed |
Briggs, R., and King, T. J. (1952). Transplantation of living nuclei from blastula cells into enucleated frogs’ eggs. Proc. Natl Acad. Sci. USA 38, 455–463.
| Transplantation of living nuclei from blastula cells into enucleated frogs’ eggs.Crossref | GoogleScholarGoogle Scholar | 16589125PubMed |
Carroll, J., and Marangos, P. (2013). The DNA damage response in mammalian oocytes. Front. Genet. 4, 117.
| The DNA damage response in mammalian oocytes.Crossref | GoogleScholarGoogle Scholar | 23805152PubMed |
Ciccia, A., and Elledge, S. J. (2010). The DNA damage response: making it safe to play with knives. Mol. Cell 40, 179–204.
| The DNA damage response: making it safe to play with knives.Crossref | GoogleScholarGoogle Scholar | 20965415PubMed |
Corrêa, G. A., Rumpf, R., Mundim, T. C., Franco, M. M., and Dode, M. A. (2008). Oxygen tension during in vitro culture of bovine embryos: effect in production and expression of genes related to oxidative stress. Anim. Reprod. Sci. 104, 132–142.
| Oxygen tension during in vitro culture of bovine embryos: effect in production and expression of genes related to oxidative stress.Crossref | GoogleScholarGoogle Scholar | 17350772PubMed |
Costa-Borges, N., Gonzalez, S., Santaló, J., and Ibáñez, E. (2011). Effect of the enucleation procedure on the reprogramming potential and developmental capacity of mouse cloned embryos treated with valproic acid. Reproduction 141, 789–800.
| Effect of the enucleation procedure on the reprogramming potential and developmental capacity of mouse cloned embryos treated with valproic acid.Crossref | GoogleScholarGoogle Scholar | 21444624PubMed |
Coticchio, G., Dal Canto, M., Mignini Renzini, M., Guglielmo, M. C., Brambillasca, F., Turchi, D., Novara, P. V., and Fadini, R. (2015). Oocyte maturation: gamete-somatic cells interactions, meiotic resumption, cytoskeletal dynamics and cytoplasmic reorganization. Hum. Reprod. Update 21, 427–454.
| Oocyte maturation: gamete-somatic cells interactions, meiotic resumption, cytoskeletal dynamics and cytoplasmic reorganization.Crossref | GoogleScholarGoogle Scholar | 25744083PubMed |
Edwards, R. G. (1965). Maturation in vitro of mouse, sheep, cow, pig, rhesus monkey and human ovary oocytes. Nature 208, 349–351.
| Maturation in vitro of mouse, sheep, cow, pig, rhesus monkey and human ovary oocytes.Crossref | GoogleScholarGoogle Scholar | 4957259PubMed |
Fabian, D., Makarevich, A. V., Chrenek, P., Bukovská, A., and Koppel, J. (2007). Chronological appearance of spontaneous and induced apoptosis during preimplantation development of rabbit and mouse embryos. Theriogenology 68, 1271–1281.
| Chronological appearance of spontaneous and induced apoptosis during preimplantation development of rabbit and mouse embryos.Crossref | GoogleScholarGoogle Scholar | 17915306PubMed |
Fabian, D., Cikos, S., and Koppel, J. (2009). Gene expression in mouse preimplantation embryos affected by apoptotic inductor actinomycin D. J. Reprod. Dev. 55, 576–582.
| Gene expression in mouse preimplantation embryos affected by apoptotic inductor actinomycin D.Crossref | GoogleScholarGoogle Scholar | 19602847PubMed |
Fulka, J., and Moor, R. M. (1993). Noninvasive chemical enucleation of mouse oocytes. Mol. Reprod. Dev. 34, 427–430.
| Noninvasive chemical enucleation of mouse oocytes.Crossref | GoogleScholarGoogle Scholar | 8471262PubMed |
Fulka, J., Loi, P., Fulka, H., Ptak, G., and Nagai, T. (2004). Nucleus transfer in mammals: noninvasive approaches for the preparation of cytoplasts. Trends Biotechnol. 22, 279–283.
| Nucleus transfer in mammals: noninvasive approaches for the preparation of cytoplasts.Crossref | GoogleScholarGoogle Scholar | 15158056PubMed |
Gjørret, J. O., Wengle, J., Maddox-Hyttel, P., and King, W. A. (2005). Chronological appearance of apoptosis in bovine embryos reconstructed by somatic cell nuclear transfer from quiescent granulosa cells. Reprod. Domest. Anim. 40, 210–216.
| Chronological appearance of apoptosis in bovine embryos reconstructed by somatic cell nuclear transfer from quiescent granulosa cells.Crossref | GoogleScholarGoogle Scholar | 15943694PubMed |
Grøndahl, C., Lessl, M., Faerge, I., Hegele-Hartung, C., Wassermann, K., and Ottesen, J. L. (2000). Meiosis-activating sterol-mediated resumption of meiosis in mouse oocytes in vitro is influenced by protein synthesis inhibition and cholera toxin. Biol. Reprod. 62, 775–780.
| Meiosis-activating sterol-mediated resumption of meiosis in mouse oocytes in vitro is influenced by protein synthesis inhibition and cholera toxin.Crossref | GoogleScholarGoogle Scholar | 10684823PubMed |
Gurdon, J. B. (1960). The effects of ultraviolet irradiation on the uncleaved eggs of Xenopus laevis. Q. J. Microsc. Sci. 101, 299–312.
Gurdon, J. B., Elsdale, T. R., and Fischberg, M. (1958). Sexually mature individuals of Xenopus laevis from the transplantation of single somatic nuclei. Nature 182, 64–65.
| Sexually mature individuals of Xenopus laevis from the transplantation of single somatic nuclei.Crossref | GoogleScholarGoogle Scholar | 13566187PubMed |
Hikawa, N., and Takenaka, T. (1996). Improved method for producing neuronal hybrids using emetine and actinomycin D. Brain Res. 734, 345–348.
| Improved method for producing neuronal hybrids using emetine and actinomycin D.Crossref | GoogleScholarGoogle Scholar | 8896846PubMed |
Hosseini, S. M., Hajian, M., Moulavi, F., Asgari, V., Forouzanfar, M., and Nasr-Esfahani, M. H. (2013). Cloned sheep blastocysts derived from oocytes enucleated manually using a pulled Pasteur pipette. Cell. Reprogram. 15, 15–23.
| Cloned sheep blastocysts derived from oocytes enucleated manually using a pulled Pasteur pipette.Crossref | GoogleScholarGoogle Scholar | 23379580PubMed |
Hosseini, S. M., Hajian, M., Forouzanfar, M., Ostadhosseini, S., Moulavi, F., Ghanaei, H. R., Gourbai, H., Shahverdi, A. H., Vosough, A. D., and Nasr-Esfahani, M. H. (2015). Chemically assisted somatic cell nuclear transfer without micromanipulator in the goat: effects of demecolcine, cytochalasin-B, and MG-132 on the efficiency of a manual method of oocyte enucleation using a pulled Pasteur pipette. Anim. Reprod. Sci. 158, 11–18.
| Chemically assisted somatic cell nuclear transfer without micromanipulator in the goat: effects of demecolcine, cytochalasin-B, and MG-132 on the efficiency of a manual method of oocyte enucleation using a pulled Pasteur pipette.Crossref | GoogleScholarGoogle Scholar | 25956201PubMed |
Iuso, D., Czernik, M., Zacchini, F., Ptak, G., and Loi, P. (2013). A simplified approach for oocyte enucleation in mammalian cloning. Cell. Reprogram. 15, 490–494.
| A simplified approach for oocyte enucleation in mammalian cloning.Crossref | GoogleScholarGoogle Scholar | 24219576PubMed |
Kim, T. M., Hwang, W. S., Shin, J. H., Park, H. J., Han, J. Y., and Lim, J. M. (2004). Development of a nonmechanical enucleation method using X-ray irradiation in somatic cell nuclear transfer. Fertil. Steril. 82, 963–965.
| Development of a nonmechanical enucleation method using X-ray irradiation in somatic cell nuclear transfer.Crossref | GoogleScholarGoogle Scholar | 15482782PubMed |
Kim, H. K., Kong, M. Y., Jeong, M. J., Han, D. C., Choi, J. D., Kim, H. Y., Yoon, K. S., Kim, J. M., Son, K. H., and Kwon, B. M. (2005). Investigation of cell cycle arrest effects of actinomycin D at G1 phase using proteomic methods in B104-1-1 cells. Int. J. Biochem. Cell Biol. 37, 1921–1929.
| Investigation of cell cycle arrest effects of actinomycin D at G1 phase using proteomic methods in B104-1-1 cells.Crossref | GoogleScholarGoogle Scholar | 15964235PubMed |
Kishigami, S., Wakayama, S., Van Thuan, N., Ohta, H., Mizutani, E., Hikichi, T., Bui, H. T., Balbach, S., Ogura, A., Boiani, M., and Wakayama, T. (2006). Production of cloned mice by somatic cell nuclear transfer. Nat. Protoc. 1, 125–138.
| Production of cloned mice by somatic cell nuclear transfer.Crossref | GoogleScholarGoogle Scholar | 17406224PubMed |
Kocabas, A. M., Crosby, J., Ross, P. J., Otu, H. H., Beyhan, Z., Can, H., Tam, W. L., Rosa, G. J., Halgren, R. G., Lim, B., Fernandez, E., and Cibelli, J. B. (2006). The transcriptome of human oocytes. Proc. Natl Acad. Sci. USA 103, 14027–14032.
| The transcriptome of human oocytes.Crossref | GoogleScholarGoogle Scholar | 16968779PubMed |
Kuetemeyer, K., Lucas-Hahn, A., Petersen, B., Lemme, E., Hassel, P., Niemann, H., and Heisterkamp, A. (2010). Combined multiphoton imaging and automated functional enucleation of porcine oocytes using femtosecond laser pulses. J. Biomed. Opt. 15, 046006.
| Combined multiphoton imaging and automated functional enucleation of porcine oocytes using femtosecond laser pulses.Crossref | GoogleScholarGoogle Scholar | 20799808PubMed |
Kyogoku, H., Yoshida, S., and Kitajima, T. S. (2018). Cytoplasmic removal, enucleation, and cell fusion of mouse oocytes. Methods Cell Biol. 144, 459–474.
| Cytoplasmic removal, enucleation, and cell fusion of mouse oocytes.Crossref | GoogleScholarGoogle Scholar | 29804683PubMed |
Lan, G. C., Wu, Y. G., Han, D., Ge, L., Liu, Y., Wang, H. L., Wang, J. Z., and Tan, J. H. (2008). Demecolcine-assisted enucleation of goat oocytes: protocol optimization, mechanism investigation, and application to improve the developmental potential of cloned embryos. Cloning Stem Cells 10, 189–202.
| Demecolcine-assisted enucleation of goat oocytes: protocol optimization, mechanism investigation, and application to improve the developmental potential of cloned embryos.Crossref | GoogleScholarGoogle Scholar | 18373477PubMed |
Li, G. P., White, K. L., and Bunch, T. D. (2004). Review of enucleation methods and procedures used in animal cloning: state of the art. Cloning Stem Cells 6, 5–13.
| Review of enucleation methods and procedures used in animal cloning: state of the art.Crossref | GoogleScholarGoogle Scholar | 15107241PubMed |
Li, G. P., Bunch, T. D., White, K. L., Rickords, L., Liu, Y., and Sessions, B. R. (2006). Denuding and centrifugation of maturing bovine oocytes alters oocyte spindle integrity and the ability of cytoplasm to support parthenogenetic and nuclear transfer embryo development. Mol. Reprod. Dev. 73, 446–451.
| Denuding and centrifugation of maturing bovine oocytes alters oocyte spindle integrity and the ability of cytoplasm to support parthenogenetic and nuclear transfer embryo development.Crossref | GoogleScholarGoogle Scholar | 16425229PubMed |
Li, J., Villemoes, K., Zhang, Y., Du, Y., Kragh, P. M., Purup, S., Xue, Q., Pedersen, A. M., Jørgensen, A. L., Jakobsen, J. E., Bolund, L., Yang, H., and Vajta, G. (2009). Efficiency of two enucleation methods connected to handmade cloning to produce transgenic porcine embryos. Reprod. Domest. Anim. 44, 122–127.
| Efficiency of two enucleation methods connected to handmade cloning to produce transgenic porcine embryos.Crossref | GoogleScholarGoogle Scholar | 18564317PubMed |
Li, S., Kang, J. D., Jin, J. X., Hong, Y., Zhu, H. Y., Jin, L., Gao, Q. S., Yan, C. G., Cui, C. D., Li, W. X., and Yin, X. J. (2014). Effect of demecolcine-assisted enucleation on the MPF level and cyclin B1 distribution in porcine oocytes. PLoS One 9, e91483.
| Effect of demecolcine-assisted enucleation on the MPF level and cyclin B1 distribution in porcine oocytes.Crossref | GoogleScholarGoogle Scholar | 25551820PubMed |
Matoba, S., and Zhang, Y. (2018). Somatic cell nuclear transfer reprogramming: mechanisms and applications. Cell Stem Cell 23, 471–485.
| Somatic cell nuclear transfer reprogramming: mechanisms and applications.Crossref | GoogleScholarGoogle Scholar | 30033121PubMed |
McGrath, J., and Solter, D. (1983). Nuclear transplantation in the mouse embryo by microsurgery and cell fusion. Science 220, 1300–1302.
| Nuclear transplantation in the mouse embryo by microsurgery and cell fusion.Crossref | GoogleScholarGoogle Scholar | 6857250PubMed |
Ménézo, Y., Dale, B., and Cohen, M. (2010). DNA damage and repair in human oocytes and embryos: a review. Zygote 18, 357–365.
| DNA damage and repair in human oocytes and embryos: a review.Crossref | GoogleScholarGoogle Scholar | 20663262PubMed |
Moura, M. T., Sousa, R. V., Leme, L. O., and Rumpf, R. (2008). Analysis of actinomycin D treated cattle oocytes and their use for somatic cell nuclear transfer. Anim. Reprod. Sci. 109, 40–49.
| Analysis of actinomycin D treated cattle oocytes and their use for somatic cell nuclear transfer.Crossref | GoogleScholarGoogle Scholar | 18162337PubMed |
Ogura, A. (2017). Cloning mice. Cold Spring Harb. Protoc. 2017, t094425.
| Cloning mice.Crossref | GoogleScholarGoogle Scholar | 28765301PubMed |
Paramanathan, T., Vladescu, L., McCauley, M. J., Rouzina, I., and Williams, M. C. (2012). Force spectroscopy reveals the DNA structural dynamics that govern the slow binding of Actinomycin D. Nucleic Acids Res. 40, 4925–4932.
| Force spectroscopy reveals the DNA structural dynamics that govern the slow binding of Actinomycin D.Crossref | GoogleScholarGoogle Scholar | 22328730PubMed |
Saraiva, N. Z., Oliveira, C. S., Leal, C. L. V., de Lima, M. R., Del Collado, M., Vantini, R., Monteiro, F. M., Niciura, S. C., and Garcia, J. M. (2015). Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts. Zygote 23, 852–862.
| Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts.Crossref | GoogleScholarGoogle Scholar | 25318529PubMed |
Sobell, H. M. (1985). Actinomycin and DNA transcription. Proc. Natl Acad. Sci. USA 82, 5328–5331.
| Actinomycin and DNA transcription.Crossref | GoogleScholarGoogle Scholar | 2410919PubMed |
Solter, D. (2000). Mammalian cloning: advances and limitations. Nat. Rev. Genet. 1, 199–207.
| Mammalian cloning: advances and limitations.Crossref | GoogleScholarGoogle Scholar | 11252749PubMed |
Tani, T., Shimada, H., Kato, Y., and Tsunoda, Y. (2006). Demecolcine-assisted enucleation for bovine cloning. Cloning Stem Cells 8, 61–66.
| Demecolcine-assisted enucleation for bovine cloning.Crossref | GoogleScholarGoogle Scholar | 16571078PubMed |
Tatemoto, H., and Terada, T. (1995). Time-dependent effects of cycloheximide and alpha-amanitin on meiotic resumption and progression in bovine follicular oocytes. Theriogenology 43, 1107–1113.
| Time-dependent effects of cycloheximide and alpha-amanitin on meiotic resumption and progression in bovine follicular oocytes.Crossref | GoogleScholarGoogle Scholar | 16727697PubMed |
Vajta, G. (2007). Handmade cloning: the future way of nuclear transfer? Trends Biotechnol. 25, 250–253.
| Handmade cloning: the future way of nuclear transfer?Crossref | GoogleScholarGoogle Scholar | 17434218PubMed |
Wagoner, E. J., Rosenkrans, C. F., Gliedt, D. W., Pierson, J. N., and Munyon, A. L. (1996). Functional enucleation of bovine oocytes: effects of centrifugation and ultraviolet light. Theriogenology 46, 279–284.
| Functional enucleation of bovine oocytes: effects of centrifugation and ultraviolet light.Crossref | GoogleScholarGoogle Scholar | 16727897PubMed |
Wakamatsu, Y., Ju, B., Pristyaznhyuk, I., Niwa, K., Ladygina, T., Kinoshita, M., Araki, K., and Ozato, K. (2001). Fertile and diploid nuclear transplants derived from embryonic cells of a small laboratory fish, medaka (Oryzias latipes). Proc. Natl Acad. Sci. USA 98, 1071–1076.
| Fertile and diploid nuclear transplants derived from embryonic cells of a small laboratory fish, medaka (Oryzias latipes).Crossref | GoogleScholarGoogle Scholar | 11158596PubMed |
Wilmut, I., Beaujean, N., Sousa, P. A., Dinnyes, A., King, T. J., Paterson, L. A., Wells, D. N., and Young, L. E. (2002). Somatic cell nuclear transfer. Nature 419, 583–587.
| Somatic cell nuclear transfer.Crossref | GoogleScholarGoogle Scholar | 12374931PubMed |
Yokoo, M., and Sato, E. (2004). Cumulus–oocyte complex interactions during oocyte maturation. Int. Rev. Cytol. 235, 251–291.
| Cumulus–oocyte complex interactions during oocyte maturation.Crossref | GoogleScholarGoogle Scholar | 15219785PubMed |
You, Z., Bailis, J. M., Johnson, S. A., Dilworth, S. M., and Hunter, T. (2007). Rapid activation of ATM on DNA flanking double-strand breaks. Nat. Cell Biol. 9, 1311–1318.
| Rapid activation of ATM on DNA flanking double-strand breaks.Crossref | GoogleScholarGoogle Scholar | 17952060PubMed |