He Xiaoyan, Tan Cheng, Li Zicong, Zhao Chengfa, Shi Junsong, Zhou Rong, Wang Xingwang, Jiang Gelong, Cai Gengyuan, Liu Dewu, Wu Zhenfang
National Engineering Research Center for Breeding Swine Industry, College of Animal Science, South China Agricultural University, Guangzhou 510642, China.
Wen's Group Academy, Wen's Foodstuff Group Co., Ltd, Yunfu 527400, China, China.
Biol Open. 2019 Apr 23;8(4):bio039917. doi: 10.1242/bio.039917.
Somatic cell nuclear transfer (SCNT) is the only method known to rapidly reprogram differentiated cells into totipotent embryos. Most cloned embryos become arrested before implantation and the details of the underlying molecular mechanism remain largely unknown. Dynamic regulation of the transcriptome is a key molecular mechanism driving early embryonic development. Here, we report comprehensive transcriptomic analysis of cloned embryos (from Laiwu and Duroc pigs) and fertilized embryos (from Duroc pigs) using RNA-sequencing. Comparisons between gene expression patterns were performed according to differentially expressed genes, specific-expressed genes, first-expressed genes, pluripotency genes and pathway enrichment analysis. In addition, we closely analyzed the improperly expressed histone lysine methyltransferases and histone lysine demethylases during cell reprogramming in cloned embryos. In summary, we identified altered gene expression profiles in porcine cloned pre-implantation embryos in comparison to normal embryos. Our findings provide a substantial framework for further discovery of the epigenetic reprogramming mechanisms in porcine SCNT embryos.
体细胞核移植(SCNT)是目前已知的将分化细胞快速重编程为全能胚胎的唯一方法。大多数克隆胚胎在植入前就会停滞发育,其潜在分子机制的细节在很大程度上仍不清楚。转录组的动态调控是驱动早期胚胎发育的关键分子机制。在此,我们报告了利用RNA测序对克隆胚胎(来自莱芜猪和杜洛克猪)和受精胚胎(来自杜洛克猪)进行的全面转录组分析。根据差异表达基因、特异性表达基因、首次表达基因、多能性基因和通路富集分析对基因表达模式进行了比较。此外,我们还密切分析了克隆胚胎细胞重编程过程中表达异常的组蛋白赖氨酸甲基转移酶和组蛋白赖氨酸去甲基化酶。总之,与正常胚胎相比,我们鉴定出了猪克隆植入前胚胎中改变的基因表达谱。我们的研究结果为进一步发现猪SCNT胚胎中的表观遗传重编程机制提供了一个重要框架。