| Literature DB >> 33478599 |
Yun Feng1, Xin Zhao1,2, Zhengda Li1, Chan Luo1, Ziyun Ruan1, Jie Xu1, Penglei Shen1, Yanfei Deng1, Jianrong Jiang1, Deshun Shi1, Fenghua Lu1.
Abstract
Somatic cell nuclear transfer (SCNT) holds vast potential in agriculture. However, its applications are still limited by its low efficiency. Histone 3 lysine 9 trimethylation (H3K9me3) was identified as an epigenetic barrier for this. Histone demethylase KDM4D could regulate the level of H3K9me3. However, its effects on buffalo SCNT embryos are still unclear. Thus, we performed this study to explore the effects and underlying mechanism of KDM4D on buffalo SCNT embryos. The results revealed that compared with the IVF embryos, the expression level of KDM4D in SCNT embryos was significantly lower at 8- and 16-cell stage, while the level of H3K9me3 in SCNT embryos was significantly higher at 2-cell, 8-cell, and blastocyst stage. Microinjection of KDM4D mRNA could promote the developmental ability of buffalo SCNT embryos. Furthermore, the expression level of ZGA-related genes such as ZSCAN5B, SNAI1, eIF-3a, and TRC at the 8-cell stage was significantly increased. Meanwhile, the pluripotency-related genes like POU5F1, SOX2, and NANOG were also significantly promoted at the blastocyst stage. The results were reversed after KDM4D was inhibited. Altogether, these results revealed that KDM4D could correct the H3K9me3 level, increase the expression level of ZGA and pluripotency-related genes, and finally, promote the developmental competence of buffalo SCNT embryos.Entities:
Keywords: KDM4D; buffalo; histone demethylation; somatic cell nuclear transfer (SCNT)
Year: 2021 PMID: 33478599 DOI: 10.1017/S1431927620024964
Source DB: PubMed Journal: Microsc Microanal ISSN: 1431-9276 Impact factor: 4.127