Selokar Naresh L, Saini Monika, Agrawal Himanshu, Palta Prabhat, Chauhan Manmohan Singh, Manik Radheysham, Singla Suresh Kumar
1 Animal Biotechnology Centre, National Dairy Research Institute , Karnal, India .
2 Department of Animal Physiology and Reproduction, Central Institute for Research on Buffaloes , Hisar, India .
Cell Reprogram. 2017 Feb;19(1):10-18. doi: 10.1089/cell.2016.0029. Epub 2017 Jan 5.
Use of histone deacetylase inhibitors (HDACis) is believed to improve the developmental competence and quality of cloned embryos produced. We examined the effects of treatment of buffalo fibroblasts with valproic acid (VPA), a HDACi on these cells and on embryos produced from them by hand-made cloning. VPA treatment (1.5, 3.0, or 4.5 mM) altered (p < 0.05) the growth characteristics and relative expression level of HDAC1, DNMT1, DNMT3a, P53, and CASPASE3, and the global level of H3K9/14ac, H4K5ac, and H3K18ac but not H3K27me3 in the cells. After the use of VPA-treated donor cells for producing embryos, the cleavage and blastocyst rate, and total cell number were not significantly affected; however, the apoptotic index was lower (p < 0.05) for 3.0 or 4.5 mM VPA group than for 1.5 mM VPA group or the controls. In the cloned blastocysts, the expression level of HDAC1 was higher (p < 0.05) and CASPASE3 was lower (p < 0.05), whereas that of DNMT1, DNMT3a, and P53 and the global level of H3K9/14ac were not significantly affected after VPA treatment of donor cells. In conclusion, these results suggest that VPA treatment of donor cells adversely affects their growth characteristics, increases histone acetylation, and alters gene expression but does not improve production rate of cloned embryos.
组蛋白去乙酰化酶抑制剂(HDACis)的使用被认为可提高所产生克隆胚胎的发育能力和质量。我们研究了用丙戊酸(VPA,一种HDACi)处理水牛成纤维细胞对这些细胞以及通过手工克隆由它们产生的胚胎的影响。VPA处理(1.5、3.0或4.5 mM)改变了(p < 0.05)细胞中HDAC1、DNMT1、DNMT3a、P53和CASPASE3的生长特性和相对表达水平,以及H3K9/14ac、H4K5ac和H3K18ac的整体水平,但未改变H3K27me3的水平。在使用经VPA处理的供体细胞生产胚胎后,卵裂率、囊胚率和总细胞数未受到显著影响;然而,3.0或4.5 mM VPA组的凋亡指数低于1.5 mM VPA组或对照组(p < 0.05)。在克隆囊胚中,HDAC1的表达水平较高(p < 0.05),而CASPASE3的表达水平较低(p < 0.05),而DNMT1、DNMT3a和P53的表达水平以及H3K9/14ac的整体水平在供体细胞经VPA处理后未受到显著影响。总之,这些结果表明,对供体细胞进行VPA处理会对其生长特性产生不利影响,增加组蛋白乙酰化并改变基因表达,但不会提高克隆胚胎的生产效率。