Increasing histone acetylation of cloned embryos, but not donor cells, by sodium butyrate improves their in vitro development in pigs

Cellular Reprogramming

Volumn 12, Issue 1, 2010, Pages 95-104

  Das, Ziban Chandra ^a   Gupta, Mukesh Kumar ^a   Uhm, Sang Jun ^a   Lee, Hoon Taek ^a  

^a Konkuk University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

BUTYRIC ACID; HISTONE; SHORT CHAIN FATTY ACID; SODIUM; 4',6 DIAMIDINO 2 PHENYLINDOLE; BUTYRIC ACID DERIVATIVE; FLUORESCENT DYE; INDOLE DERIVATIVE;

ACETYLATION; ANIMAL CELL; ARTICLE; BLASTOCYST; CELL CYCLE G0 PHASE; CELL CYCLE G1 PHASE; CELL CYCLE G2 PHASE; CELL CYCLE M PHASE; CELL CYCLE S PHASE; CELL MATURATION; CELL NUCLEUS; CELL NUCLEUS TRANSPLANTATION; CELL PROLIFERATION; CELL VIABILITY; CLONING; COLON; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DEGRADATION; DIETARY FIBER; EMBRYO; EXPERIMENTAL PIG; FEMALE; FERTILIZATION IN VITRO; FIBROBLAST; IN VITRO STUDY; NONHUMAN; PRIORITY JOURNAL; RECTUM; SOMATIC CELL; ANIMAL; ANIMAL EMBRYO; DOSE RESPONSE; DRUG EFFECT; EMBRYO CULTURE; EMBRYO DEVELOPMENT; METABOLISM; SWINE; TIME;

BACTERIA (MICROORGANISMS); SUIDAE;

ACETYLATION; ANIMALS; BLASTOCYST; BUTYRATES; CELL NUCLEUS; CLONING, ORGANISM; DOSE-RESPONSE RELATIONSHIP, DRUG; EMBRYO CULTURE TECHNIQUES; EMBRYO, MAMMALIAN; EMBRYONIC DEVELOPMENT; FLUORESCENT DYES; HISTONES; INDOLES; SWINE; TIME FACTORS;

EID: 77952301909     PISSN: 21524971     EISSN: 21524998     Source Type: Journal    
DOI: 10.1089/cell.2009.0068     Document Type: Article

References (46)

1. Abramova, M.V., Pospelova, T.V., Nikulenkov, F.P., et al. (2006). G1=S arrest induced by histone deacetylase inhibitor sodium butyrate in E1A\+Ras-transformed cells is mediated through down-regulation of E2F activity and stabilization of beta-catenin. J. Biol. Chem. 281, 21040-21051.
2. Bourc'his, D., Le Bourhis, D., Patin, D., et al. (2001). Delayed and incomplete reprogramming of chromosome methylation patterns in bovine cloned embryos. Curr. Biol. 11, 1542-1546.
3. Bugaut, M., and Bentejac, M. (1993). Biological effects of short-chain fatty acids in nonruminant mammals. Annu. Rev. Nutr. 13, 217-241.
4. Cuisset, L., Tichonicky, L., and Delpech, M. (1998). A protein phosphatase is involved in the inhibition of histone deacety-lation by sodium butyrate. Biochem. Biophys. Res. Commun. 246, 760-764.
5. Ding, X., Wang, Y., Zhang, D., et al. (2008). Increased pre-implantation development of cloned bovine embryos treated with 5-aza-2-deoxycytidine and trichostatin A. Theriogenol-ogy 70, 622-630.
6. Drottar, M., Liberman, M.C., Ratan, R.R., et al. (2006). The his-tone deacetylase inhibitor sodium butyrate protects against cisplatin-induced hearing loss in guinea pigs. Laryngoscope 116, 292-296.
7. Enright, B.P., Kubota, C., Yang, X., et al. (2003). Epigenetic characteristics and development of embryos cloned from donor cells treated by trichostatin A or 5-aza-2-deoxycytidine. Biol. Reprod. 69, 896-901.
8. Goicoa, S., Alvarez, S., Ricordi, C., et al. (2006). Sodium butyrate activates genes of early pancreatic development in embryonic stem cells. Cloning Stem Cells 8, 140-149.
9. Gupta, M.K., Uhm, S.J., Han, D.W., et al. (2007a). Embryo quality and production efficiency of porcine parthenotes is improved by phytohemagglutinin. Mol. Reprod. Dev. 74, 435-444.
10. Gupta, M.K., Uhm, S.J., and Lee, H.T. (2007b). Cryopre-servation of immature and in vitro matured porcine oo-cytes by solid surface vitrification. Theriogenology 67, 238-248.
11. Gupta, M.K., Uhm, S.J., and Lee, H.T. (2007c). Differential but beneficial effect of phytohemagglutinin on efficiency of in vitro porcine embryo production by somatic cell nuclear transfer or in vitro fertilization. Mol. Reprod. Dev. 74, 1557-1567.
12. Gupta, M.K., Uhm, S.J., and Lee, H.T. (2008a). Sexual maturity and reproductive phase of oocyte donor influence the developmental ability and apoptosis of cloned and par-thenogenetic porcine embryos. Anim. Reprod. Sci. 108, 107-121.
13. Gupta, M.K., Uhm, S.J., Lee, S.H., et al. (2008b). Role of nones-sential amino acids on porcine embryos produced by parthenogenesis or somatic cell nuclear transfer. Mol. Reprod. Dev. 75, 588-597.
14. Gupta, M.K., Jang, J.M., Jung, J.W., et al. (2009). Proteomic analysis of parthenogenetic and in vitro fertilized porcine embryos. Proteomics 9, 2846-2860.
15. Hochedlinger, K., and Jaenisch, R. (2006). Nuclear reprogram-ming and pluripotency. Nature 441, 1061-1067.
16. Iager, A.E., Ragina, N.P., Ross, P.J., et al. (2008). Trichostatin A improves histone acetylation in bovine somatic cell nuclear transfer early embryos. Cloning Stem Cells 10, 371-379.
17. Kang, Y.K., Koo, D.B., Park, J.S., et al. (2001). Typical de-methylation events in cloned pig embryos. Clues on species-specific differences in epigenetic reprogramming of a cloned donor genome. J. Biol. Chem. 276, 39980-39984.
18. Kishigami, S., Mizutani, E., Ohta, H., et al. (2006). Significant improvement of mouse cloning technique by treatment with trichostatin A after somatic nuclear transfer. Biochem. Bio-phys. Res. Commun. 340, 183-189.
19. Li, J., Svarcova, O., Villemoes, K., et al. (2008). High in vitro development after somatic cell nuclear transfer and trichos-tatin A treatment of reconstructed porcine embryos. Ther-iogenology 70, 800-808.
20. Maalouf, W.E., Liu, Z., Brochard, V., et al. (2009). Trichostatin A treatment of cloned mouse embryos improves constitutive heterochromatin remodeling as well as developmental potential to term. BMC Dev. Biol. 9, 11.
21. Meng, Q., Polgar, Z., Liu, J., et al. (2009). Live birth of somatic cell-cloned rabbits following trichostatin A treatment and co-transfer of parthenogenetic embryos. Cloning Stem Cells 11, 203-208.
22. Mohana Kumar, B., Song, H.J., Cho, S.K., et al. (2007). Effect of histone acetylation modification with sodium butyrate, a his-tone deacetylase inhibitor, on cell cycle, apoptosis, ploidy and gene expression in porcine fetal fibroblasts. J. Reprod. Dev. 53, 903-913.
23. Oback, B., and Wells, D. (2002). Donor cells for nuclear cloning: many are called, but few are chosen. Cloning Stem Cells 4, 147-168.
24. Ou, H.C., Jea-Chien, E., and Sun, S.H. (1997). Sodium butyrate decreases histamine-stimulated calcium mobilization in C6 glioma cells. Neuroreport 8, 1375-1378.
25. Rice, J.C., and Allis, C.D. (2001). Histone methylation versus histone acetylation: new insights into epigenetic regulation. Curr. Opin. Cell Biol. 13, 263-273.
26. Russo, G.L., Della Pietra, V., Mercurio, C., et al. (1997). Down-regulation of protein kinase CKII activity by sodium butyrate. Biochem. Biophys. Res. Commun. 233, 673-677.
27. Rybouchkin, A., Kato, Y., and Tsunoda, Y. (2006). Role of his-tone acetylation in reprogramming of somatic nuclei following nuclear transfer. Biol. Reprod. 74, 1083-1089.
28. Shi, L., and Wu, J. (2009). Epigenetic regulation in mammalian preimplantation embryo development. Reprod. Biol. En-docrinol. 7, 59.
29. Shi, L.H., Miao, Y.L., Ouyang, Y.C., et al. (2008). Trichostatin A (TSA) improves the development of rabbit-rabbit intraspecies cloned embryos, but not rabbit-human interspecies cloned embryos. Dev. Dyn. 237, 640-648.
30. Shi, W., Hoeflich, A., Flaswinkel, H., et al. (2003). Induction of a senescent-like phenotype does not confer the ability of bovine immortal cells to support the development of nuclear transfer embryos. Biol. Reprod. 69, 301-309.
31. Srirattana, K., Laowtammathron, C., Devahudi, R., et al. (2008). Effect of Trichostatin A on developmental potenaial of inter-species cloned gaur (Bos gaurus) embryos. Reprod. Fertil. Dev. 21, 126-126
32. Svensson, K., Mattsson, R., James, T.C., et al. (1998). The paternal allele of the H19 gene is progressively silenced during early mouse development: the acetylation status of histones may be involved in the generation of variegated expression patterns. Development 125, 61-69.
33. Tsuji, Y., Kato, Y., and Tsunoda, Y. (2009). The developmental potential of mouse somatic cell nuclear-transferred oocytes treated with trichostatin A and 5-aza-2-deoxycytidine. Zygote 17, 109-115.
34. Uhm, S.J., Gupta, M.K., Kim, T., et al. (2007). Expression of enhanced green fluorescent protein in porcine-and bovine-cloned embryos following interspecies somatic cell nuclear transfer of fibroblasts transfected by retrovirus vector. Mol. Reprod. Dev. 74, 1538-1547.
35. Uhm, S.J., Gupta, M.K., Das, Z.C., et al. (2009). Effect of trans-gene introduction and recloning on efficiency of porcine transgenic cloned embryo production in vitro. Reprod. Domest. Anim. 44, 106-115.
36. Van Thuan, N., Bui, H.T., Kim, J.H., et al. (2009). The histone deacetylase inhibitor scriptaid enhances nascent mRNA production and rescues full-term development in cloned inbred mice. Reproduction 138, 309-317.
37. VerMilyea, M.D., O'Neill, L.P., and Turner, B.M. (2009). Transcription-independent heritability of induced histone modifications in the mouse preimplantation embryo. PLoS One 4, e6086.
38. Wakayama, S., Li, C., Ono, T., et al. (2008). Recloning of mice over six generations. Biol. Reprod. 78, 305.
39. Wee, G., Koo, D.B., Song, B.S., et al. (2006). Inheritable histone H4 acetylation of somatic chromatins in cloned embryos. J. Biol. Chem. 281, 6048-6057.
40. Wee, G., Shim, J.J., Koo, D.B., et al. (2007). Epigenetic alteration of the donor cells does not recapitulate the reprogramming of DNA methylation in cloned embryos. Reproduction 134, 781-787.
41. Wu, X., Li, Y., Li, G.P., et al. (2008). Trichostatin A improved epigenetic modifications of transfected cells but did not improve subsequent cloned embryo development. Anim. Bio-technol. 19, 211-224.
42. Yamanaka, K.I., Sugimura, S., Wakai, T., et al. (2009). Acet-ylation level of histone H3 in early embryonic stages affects subsequent development of miniature pig somatic cell nuclear transfer Embryos. J. Reprod. Dev. [Epub ahead of print].
43. Yang, F., Hao, R., Kessler, B., et al. (2007). Rabbit somatic cell cloning: effects of donor cell type, histone acetylation status and chimeric embryo complementation. Reproduction 133, 219-230.
44. Yeo, S., Lee, K.K., Han, Y.M., et al. (2005). Methylation changes of lysine 9 of histone H3 during preimplantation mouse development. Mol Cells 20, 423-428.
45. Zhang, Y., Li, J., Villemoes, K., et al. (2007). An epigenetic modifier results in improved in vitro blastocyst production after somatic cell nuclear transfer. Cloning Stem Cells 9, 357-363.
46. Zhao, J., Ross, J.W., Hao, Y., et al. (2009). Significant improvement in cloning efficiency of an inbred miniature pig by his-tone deacetylase inhibitor treatment after somatic cell nuclear transfer. Biol. Reprod. 81, 525-530.