Dynamic Change Patterns of H3K64ac in Early Development of Porcine (Sus scrofa domesticus) Somatic Cell Cloned Embryos
ZHANG Dan-Dan, XU Teng-Teng, GAO Di, NING Wei, QI Xin, RU Zhen-Yuan, ZHANG Xiang-Dong, LI Yun-Sheng, ZHANG Yun-Hai, CAO Zu-Bing*
Anhui Provincial Key Laboratory of Livestock and Poultry Genetic Resources Protection and Biological breeding, College of Animal Science and Technology, Anhui Agricultural University, Hefei 230036, China
Abstract:Histone acetylation is the first histone modification to be identified, which regulates gene expression by changing chromatin structure and accessibility, and is widely involved in the regulation of various biological events during early embryonic development of mammals. H3K64ac is a previously unidentified histone modification on the lateral surface of the histone octamer. It is known to be involved in regulating nucleosome stability and promoting gene expression in vivo. However, the role of H3K64ac in the early development of porcine (Sus scrofa domesticus) somatic nuclear transfer embryos is still unknown. In this study, H3K64ac in early embryos derived from parthenogenetic activation (PA) and somatic cell nuclear transfer (SCNT) were examined by immunofluorescence staining. PA 4-cell embryos were treated with aphidicolin, α-amanitin and cycloheximide, respectively. The results showed that H3K64ac modification was always present in both PA and SCNT embryos, and H3K64ac levels were the maximum at the pronuclear stage, decreased at the 2-cell stage, slightly increased at the 4-cell stage, and remained low status from the 8-cell stage to the blastocyst stage. Comparison analyses of H3K64ac levels between PA and SCNT embryos revealed that H3K64ac levels in SCNT embryos at each stage were significantly higher than those in PA embryos (P<0.05). Inhibition of DNA replication, RNA and protein synthesis did not affect H3K64ac levels in porcine embryos. The results suggested that H3K64ac was abnormally reprogramming during early development of porcine cloned embryos, and the reduction of H3K64ac levels in early embryonic development was an active reactive process independent of DNA replication, RNA and protein synthesis. This study provides a theoretical basis for further study on the molecular mechanism of H3K64ac involved in regulating the development of porcine somatic nuclear transfer embryos.
[1] 华再东, 郭帅, 肖红卫, 等. 2017. 体内、外卵母细胞对猪体细胞克隆胚胎发育潜力的影响[J]. 中国畜牧兽医, 44(11): 3143-3148. (Hua Z D, Guo S, Xiao H W.2017. Effect of oocytes in vivo and in vitro on the developmental potential of porcine somatic cell cloned embryos[J]. China Animal Husbandry & Veterinary Medicine, 244(11): 3143-3148.) [2] 吴霄, 庄站伟, 马晓莉, 等. 2019. 核移植介导的哺乳动物体细胞核重编程研究进展[J]. 生物技术通报, 35(11): 187-194. (Wu X, Zhuang Z W, Ma X L, et al.2019. Advances in mammalian somatic cell nuclear reprogramming mediated by nuclear transplantation[J]. Biotechnology Information, 35(11): 187-194.) [3] 杨旭琼, 吴珍芳, 李紫聪. 2019. 哺乳动物体细胞核移植表观遗传重编程研究进展[J]. 遗传, 41(12): 1099-1109. (Yang X Q, Wu Z F, Li Z C.2019. Advances in epigenetic reprogramming in mammalian somatic cell nuclear transplantation[J]. Genetics, 41(12): 1099-1109.) [4] Abmayr S M, Workman J L.2012. Holding on through DNA replication: Histone modification or modifier?[J]. Cell, 150(5): 875-877. [5] Akagi S, Matsukawa K, Mizutani E, et al.2011. Treatment with a histone deacetylase inhibitor after nuclear transfer improves the preimplantation development of cloned bovine embryos[J]. Journal of Reproduction and Development, 57(1): 120-126. [6] Bai G Y, Song S H, Zhang Y W, et al.2018. Kdm6a overexpression improves the development of cloned mouse embryos[J]. Zygote, 26(1): 24-32. [7] Cerbo D V, Mohn F, Ryan D P, et al.2014. Acetylation of histone H3 at lysine 64 regulates nucleosome dynamics and facilitates transcription[J]. Elife, 3: e01632. [8] Deshmukh R S, Ostrup O, Ostrup E, et al.2011. DNA methylation in porcine preimplantation embryos developed in vivo and produced by in vitro fertilization, parthenogenetic activation and somatic cell nuclear transfer[J]. Epigenetics, 6(2): 177-187. [9] Jin L, Guo Q, Zhang G L, et al.2018. The histone deacetylase inhibitor, CI994, improves nuclear reprogramming and in vitro developmental potential of cloned pig embryos[J]. Cell Reprogram, 20(3): 205-213. [10] Jin L, Zhu H Y, Guo Q, et al.2017. Effect of histone acetylation modification with MGCD0103, a histone deacetylase inhibitor, on nuclear reprogramming and the developmental competence of porcine somatic cell nuclear transfer embryos[J]. Theriogenology, 87: 298-305. [11] Ju S, Rui R.2012. Effects of cumulus cells on in vitro maturation of oocytes and development of cloned embryos in the pig[J]. Reproduction in Domestic Animals, 47(4): 521-529. [12] Keefer C L.2008. Lessons learned from nuclear transfer (cloning)[J]. Theriogenology, 69(1): 48-54. [13] Kishigami S.,S. Wakayama,Y. Hosoi,et al.2008. Somatic cell nuclear transfer: infinite reproduction of a unique diploid genome[J]. Experimental Cell Research, 314(9): 1945-1950. [14] Koo D B, Kang Y K, Choi Y H, et al.2000. In vitro development of reconstructed porcine oocytes after somatic cell nuclear transfer[J]. Biology of Reproduction, 63(4): 986-992. [15] Kuo M H, Allis C D.1998. Roles of histone acetyltransferases and deacetylases in gene regulation[J]. Bioessays, 20(8): 615-626. [16] Kushwaha A, Thakur M K.2020. Increase in hippocampal histone H3K9me3 is negatively correlated with memory in old male mice[J]. Biogerontology, 21(2): 175-189. [17] Lange U C, Siebert S, Wossidlo M, et al.2013. Dissecting the role of H3K64me3 in mouse pericentromeric heterochromatin[J]. Nature Communications, 4: 2233. [18] Li D, Wan C L, Bai B L, et al.2019. Identification of histone acetylation markers in human fetal brains and increased H4K5ac expression in neural tube defects[J]. Molecular Genetics & Genomic Medicine, 7(12): e1002. [19] Liu W, Liu X, Wang C, et al.2016. Identification of key factors conquering developmental arrest of somatic cell cloned embryos by combining embryo biopsy and single-cell sequencing[J]. Cell Discovery, 2(1): 16010-16025. [20] Liu X, Wang Y, Gao Y, et al.2018. H3K9 demethylase KDM4E is an epigenetic regulator for bovine embryonic development and a defective factor for nuclear reprogramming[J]. Development, 145(4): 158261-158273. [21] Luense L J, Donahue G, Lin-Shiao E, et al.2019. Gcn5-mediated histone acetylation governs nucleosome dynamics in spermiogenesis[J]. Developmental Cell, 51(6): 745-758 e746. [22] Pasini D, Malatesta M, Jung H R, et al.2010. Characterization of an antagonistic switch between histone H3 lysine 27 methylation and acetylation in the transcriptional regulation of polycomb group target genes[J]. Nucleic Acids Research, 38(15): 4958-4969. [23] Rodriguez-Osorio N, Urrego R, Cibelli J B, et al.2012. Reprogramming mammalian somatic cells[J]. Theriogenology, 78(9): 1869-1886. [24] Ross P J, Ragina N P, Rodriguez R M, et al.2008. Polycomb gene expression and histone H3 lysine 27 trimethylation changes during bovine preimplantation development[J]. Reproduction, 136(6): 777-785. [25] Santos F, Zakhartchenko V, Stojkovic M, et al.2003. Epigenetic marking correlates with developmental potential in cloned bovine preimplantation embryos[J]. Current Biology, 13(13): 1116-1121. [26] Sato Y, Hilbert L, Oda H, et al.2019. Histone H3K27 acetylation precedes active transcription during zebrafish zygotic genome activation as revealed by live-cell analysis[J]. Development, 146(19): 179127-179137. [27] Tomar J S, Hosur R V.2020. Polyamine acetylation and substrate-induced oligomeric states in histone acetyl transferase of multiple drug resistant Acinetobacter baumannii[J]. Biochimie, 168(15): 268-276. [28] Tropberger P, Pott S, Keller C, et al.2013. Regulation of transcription through acetylation of H3K122 on the lateral surface of the histone octamer[J]. Cell, 152(4): 859-872. [29] Wang Y S, Xiong X R, An Z X, et al.2011. Production of cloned calves by combination treatment of both donor cells and early cloned embryos with 5-aza-2/-deoxycytidine and trichostatin A[J]. Theriogenology, 75(5): 819-825. [30] Wilmut I, Bai Y, Taylor J.2015. Somatic cell nuclear transfer: origins, the present position and future opportunities[J]. Philosophical Transactions of the Royal Society of London B Biological Sciences, 370(1680): 20140366. [31] Yu L, Zhang X, Wang X, et al.2020. Regulation and molecular mechanism of histone acetylation modification in sevoflurane-induced POCD in mice[J]. Journal of King Saud University-Science, 32(2): 1312-1318. [32] Zhang H, Wu B, Liu H, et al.2013. Improving development of cloned goat embryos by supplementing alpha-lipoic acid to oocyte in vitro maturation medium[J]. Theriogenology, 80(3): 228-233. [33] Zhou W, Jiang D, Tian J, et al.2019. Acetylation of H3K4, H3K9, and H3K27 mediated by p300 regulates the expression of GATA4 in cardiocytes[J]. Genes Diseases, 6(3): 318-325. [34] Ziegler-Birling C, Daujat S, Schneider R, et al.2016. Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development[J]. Epigenetics, 11(8): 553-562.