Trichostatin A rescues the disrupted imprinting induced by somatic cell nuclear transfer in pigs

• Published in: PloS one 2015-05, Vol.10 (5), p.e0126607-e0126607
• Main Authors: Huan, Yanjun, Zhu, Jiang, Huang, Bo, Mu, Yanshuang, Kong, Qingran, Liu, Zhonghua
• Format: Article
• Language: English
• Subjects: Aberration; Abnormalities; Animals; Antifungal agents; Cells, Cultured; Cloning; DNA methylation; DNA Methylation - drug effects; DNA Methylation - genetics; Efficiency; Embryos; Epigenetics; Female; Fertilization in Vitro; Fetuses; Fibroblasts - drug effects; Fibroblasts - metabolism; Gene expression; Genomic imprinting; Genomic Imprinting - drug effects; Genomic Imprinting - genetics; Health aspects; Histone deacetylase; Hogs; Hydroxamic Acids - pharmacology; Imprinting; Imprinting (Psychology); Insulin-like growth factor II; Insulin-Like Growth Factor II - metabolism; Nuclear transfer; Nuclear transfer (Cloning); Nuclear Transfer Techniques; Pregnancy; Somatic cell nuclear transfer; Suidae; Swine; Trichostatin A
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0126607

Imprinting disorders induced by somatic cell nuclear transfer (SCNT) usually lead to the abnormalities of cloned animals and low cloning efficiency. Histone deacetylase inhibitors have been shown to improve gene expression, genomic methylation reprogramming and the development of cloned embryos, however, the imprinting statuses in these treated embryos and during their subsequent development remain poorly studied. In this study, we investigated the dynamics of H19/Igf2 methylation and transcription in porcine cloned embryos treated with trichostatin A (TSA), and examined H19/Igf2 imprinting patterns in cloned fetuses and piglets. Our results showed that compared with the maintenance of H19/Igf2 methylation in fertilized embryos, cloned embryos displayed aberrant H19/Igf2 methylation and lower H19/Igf2 transcripts. When TSA enhanced the development of cloned embryos, the disrupted H19/Igf2 imprinting was largely rescued in these treated embryos, more similar to those detected in fertilized counterparts. Further studies displayed that TSA effectively rescued the disrupted imprinting of H19/Igf2 in cloned fetuses and piglets, prevented the occurrence of cloned fetus and piglet abnormalities, and enhanced the full-term development of cloned embryos. In conclusion, our results demonstrated that aberrant imprinting induced by SCNT led to the abnormalities of cloned fetuses and piglets and low cloning efficiency, and TSA rescued the disrupted imprinting in cloned embryos, fetuses and piglets, and prevented the occurrence of cloned fetus and piglet abnormalities, thereby improving the development of cloned embryos. This study would have important implications in improving cloning efficiency and the health of cloned animals.