Improvement of porcine cloning efficiency by trichostain A through early-stage induction of embryo apoptosis

Theriogenology

Volumn 79, Issue 5, 2013, Pages 815-823

  Ji, Qianqian ^a   Zhu, Kongju ^a   Liu, Zhiguo ^a   Song, Zhenwei ^a   Huang, Yuankai ^a   Zhao, Haijing ^a   Chen, Yaosheng ^a   He, Zuyong ^a   Mo, Delin ^a   Cong, Peiqing ^a  

^a SUN YAT SEN UNIVERSITY   (China)

Author keywords

Apoptosis; Embryo; Nuclear transfer; Porcine; Trichostain A

Indexed keywords

HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID; TRICHOSTATIN A;

ANIMAL; ANIMAL DISEASE; ANIMAL EMBRYO; APOPTOSIS; ARTICLE; CELL NUCLEUS TRANSPLANTATION; CELL PROLIFERATION; CLONING; COMET ASSAY; DRUG EFFECT; EMBRYO DEVELOPMENT; METHODOLOGY; PRENATAL DEVELOPMENT; SWINE;

ANIMALS; APOPTOSIS; CELL PROLIFERATION; CLONING, ORGANISM; COMET ASSAY; EMBRYO, MAMMALIAN; EMBRYONIC DEVELOPMENT; HISTONE DEACETYLASE INHIBITORS; HYDROXAMIC ACIDS; NUCLEAR TRANSFER TECHNIQUES; SWINE;

SUS;

EID: 84874336702     PISSN: 0093691X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.theriogenology.2012.12.010     Document Type: Article

References (42)

1. Rogatcheva M.M., Rund L.A., Swanson K.S., Marron B.M., Beever J.E., Counter C.M., et al. Creating porcine biomedical models through recombineering. Comp Funct Genom 2004, 5:262-267.
2. Ahn K.S., Won J.Y., Heo S.Y., Kang J.H., Yang H.S., Shim H. Transgenesis and nuclear transfer using porcine embryonic germ cells. Cloning Stem Cells 2007, 9:461-468.
3. Kong Q.R., Zhu J., Huang B., Huan Y.J., Wang F., Shi Y.Q., et al. TSA improves transgenic porcine cloned embryo development and transgene expression. Yi Chuan 2011, 33:749-756. [in Chinese].
4. Wu X., Li Y., Li G.P., Yang D., Yue Y., Wang L., et al. Trichostatin A improved epigenetic modifications of transfected cells but did not improve subsequent cloned embryo development. Anim Biotechnol 2008, 19:211-224.
5. Zhang Y., Li J., Villemoes K., Pedersen A.M., Purup S., Vajta G. An epigenetic modifier results in improved in vitro blastocyst production after somatic cell nuclear transfer. Cloning Stem Cells 2007, 9:357-363.
6. Cui X.S., Xu Y.N., Shen X.H., Zhang L.Q., Zhang J.B., Kim N.H. Trichostatin A modulates apoptotic-related gene expression and improves embryo viability in cloned bovine embryos. Cell Reprogram 2011, 13:179-189.
7. Li X., Kato Y., Tsuji Y., Tsunoda Y. The effects of trichostatin A on mRNA expression of chromatin structure-, DNA methylation-, and development-related genes in cloned mouse blastocysts. Cloning Stem Cells 2008, 10:133-142.
8. Cervera R.P., Marti-Gutierrez N., Escorihuela E., Moreno R., Stojkovic M. Trichostatin A affects histone acetylation and gene expression in porcine somatic cell nucleus transfer embryos. Theriogenology 2009, 72:1097-1110.
9. Himaki T., Yokomine T.A., Sato M., Takao S., Miyoshi K., Yoshida M. Effects of trichostatin A on in vitro development and transgene function in somatic cell nuclear transfer embryos derived from transgenic Clawn miniature pig cells. Anim Sci J 2010, 81:558-563.
10. Woo H.J., Lee S.J., Choi B.T., Park Y.M., Choi Y.H. Induction of apoptosis and inhibition of telomerase activity by trichostatin A, a histone deacetylase inhibitor, in human leukemic U937 cells. Exp Mol Pathol 2007, 82:77-84.
11. Ranganathan P., Rangnekar V.M. Exploiting the TSA connections to overcome apoptosis-resistance. Cancer Biol Ther 2005, 4:391-392.
12. Zhu S., Li Y., Zhao L., Hou P., Shangguan C., Yao R., et al. TSA-induced JMJD2B downregulation is associated with Cyclin B1-dependent survivin degradation and apoptosis in LNCap cells. J Cell Biochem 2012, 113:2375-2382.
13. Fabian D., Koppel J., Maddox-Hyttel P. Apoptotic processes during mammalian preimplantation development. Theriogenology 2005, 64:221-231.
14. Metcalfe A.D., Hunter H.R., Bloor D.J., Lieberman B.A., Picton H.M., Leese H.J., et al. Expression of 11 members of the BCL-2 family of apoptosis regulatory molecules during human preimplantation embryo development and fragmentation. Mol Reprod Dev 2004, 68:35-50.
15. Cong P.Q., Kim E.S., Song E.S., Yi Y.J., Park C.S. Effects of fusion/activation methods on development of embryos produced by nuclear transfer of porcine fetal fibroblast. Anim Reprod Sci 2008, 103:304-311.
16. Yoshioka K., Suzuki C., Tanaka A., Anas I.M., Iwamura S. Birth of piglets derived from porcine zygotes cultured in a chemically defined medium. Biol Reprod 2002, 66:112-119.
17. Ju S., Rui R., Lu Q., Lin P., Guo H. Analysis of apoptosis and methyltransferase mRNA expression in porcine cloned embryos cultured in vitro. J Assist Reprod Genet 2010, 27:49-59.
18. Fabian D., Rehak P., Czikkova S., Il'kova G., Baran V., Koppel J. Induced cell death of preimplantation mouse embryos cultured in vitro evaluated by comet assay. Theriogenology 2003, 60:691-706.
19. Jeon Y., Jeong S.H., Biswas D., Jung E.M., Jeung E.B., Lee E.S., et al. Cleavage pattern and survivin expression in porcine embryos by somatic cell nuclear transfer. Theriogenology 2011, 76:1187-1196.
20. Xu S.J., Xu Y.X., Liu H.L. Mechanisms of epigenetic reprogramming in Mammalian resonstructed embryos produced by nuclear transfer. Yi Chuan 2005, 27:473-480. [in Chinese].
21. Latham K.E. Early and delayed aspects of nuclear reprogramming during cloning. Biol Cell 2005, 97:119-132.
22. Kishigami S., Wakayama S., Thuan N.V., Ohta H., Mizutani E., Hikichi T., et al. Production of cloned mice by somatic cell nuclear transfer. Nat Protoc 2006, 1:125-138.
23. Kishigami S., Mizutani E., Ohta H., Hikichi T., Thuan N.V., Wakayama S., et al. Significant improvement of mouse cloning technique by treatment with trichostatin A after somatic nuclear transfer. Biochem Biophys Res Commun 2006, 340:183-189.
24. Shi L.H., Miao Y.L., Ouyang Y.C., Huang J.C., Lei Z.L., Yang J.W., et al. Trichostatin A (TSA) improves the development of rabbit-rabbit intraspecies cloned embryos, but not rabbit-human interspecies cloned embryos. Dev Dyn 2008, 237:640-648.
25. Kishigami S., Bui H.T., Wakayama S., Tokunaga K., Van Thuan N., Hikichi T., et al. Successful mouse cloning of an outbred strain by trichostatin A treatment after somatic nuclear transfer. J Reprod Dev 2007, 53:165-170.
26. Wetzel M., Premkumar D.R., Arnold B., Pollack I.F. Effect of trichostatin A, a histone deacetylase inhibitor, on glioma proliferation in vitro by inducing cell cycle arrest and apoptosis. J Neurosurg 2005, 103:549-556.
27. Taghiyev A.F., Guseva N.V., Sturm M.T., Rokhlin O.W., Cohen M.B. Trichostatin A (TSA) sensitizes the human prostatic cancer cell line DU145 to death receptor ligands treatment. Cancer Biol Ther 2005, 4:382-390.
28. Telford N.A., Watson A.J., Schultz G.A. Transition from maternal to embryonic control in early mammalian development: a comparison of several species. Mol Reprod Dev 1990, 26:90-100.
29. Brill A., Torchinsky A., Carp H., Toder V. The role of apoptosis in normal and abnormal embryonic development. J Assist Reprod Genet 1999, 16:512-519.
30. Shi L.H., Ai J.S., Ouyang Y.C., Huang J.C., Lei Z.L., Wang Q., et al. Trichostatin A and nuclear reprogramming of cloned rabbit embryos. J Anim Sci 2008, 86:1106-1113.
31. Li Z., Jo J., Jia J.M., Lo S.C., Whitcomb D.J., Jiao S., et al. Caspase-3 activation via mitochondria is required for long-term depression and AMPA receptor internalization. Cell 2010, 141:859-871.
32. Earnshaw W.C., Martins L.M., Kaufmann S.H. Mammalian caspases: structure, activation, substrates, and functions during apoptosis. Annu Rev Biochem 1999, 68:383-424.
33. Porter A.G., Janicke R.U. Emerging roles of caspase-3 in apoptosis. Cell Death Differ 1999, 6:99-104.
34. Hirata H., Takahashi A., Kobayashi S., Yonehara S., Sawai H., Okazaki T., et al. Caspases are activated in a branched protease cascade and control distinct downstream processes in Fas-induced apoptosis. J Exp Med 1998, 187:587-600.
35. Woo M., Hakem R., Soengas M.S., Duncan G.S., Shahinian A., Kagi D., et al. Essential contribution of caspase 3/CPP32 to apoptosis and its associated nuclear changes. Genes Dev 1998, 12:806-819.
36. Jänicke R.U., Sprengart M.L., Wati M.R., Porter A.G. Caspase-3 is required for DNA fragmentation and morphological changes associated with apoptosis. J Biol Chem 1998, 273:9357-9360.
37. Kuida K., Zheng T.S., Na S., Kuan C., Yang D., Karasuyama H., et al. Decreased apoptosis in the brain and premature lethality in CPP32-deficient mice. Nature 1996, 384:368-372.
38. Li F., Srinivasan A., Wang Y., Armstrong R.C., Tomaselli K.J., Fritz L.C. Cell-specific induction of apoptosis by microinjection of cytochrome c. Bcl-xL has activity independent of cytochrome c release. J Biol Chem 1997, 272:30299-30305.
39. Chauhan D., Pandey P., Ogata A., Teoh G., Krett N., Halgren R., et al. Cytochrome c-dependent and -independent induction of apoptosis in multiple myeloma cells. J Biol Chem 1997, 272:29995-29997.
40. Finucane D.M., Bossy-Wetzel E., Waterhouse N.J., Cotter T.G., Green D.R. Bax-induced caspase activation and apoptosis via cytochrome c release from mitochondria is inhibitable by Bcl-xL. J Biol Chem 1999, 274:2225-2233.
41. Sharma M., Kumar R., Dubey P.K., Verma O.P., Nath A., Saikumar G., et al. Expression and quantification of Oct-4 gene in blastocyst and embryonic stem cells derived from in vitro produced buffalo embryos. In Vitro Cell Dev Biol Anim 2012, 48:229-235.
42. Chambers I., Silva J., Colby D., Nichols J., Nijmeijer B., Robertson M., et al. Nanog safeguards pluripotency and mediates germline development. Nature 2007, 450:1230-1234.