Bai Lin, Li Mengqi, Sun Junli, Yang Xiaogan, Lu Yangqing, Lu Shengsheng, Lu Kehuan
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi University, No. 100 Daxue Road, Xixiangtang District, Nanning, Guangxi Zhuang Autonomous Region.530004, China.
Guangxi High Education Laboratory for Animal Reproduction and Biotechnology, Guangxi University, No. 100 Daxue Road, Xixiangtang District, Nanning, Guangxi Zhuang Autonomous Region.530004, China.
PLoS One. 2016 Apr 12;11(4):e0153093. doi: 10.1371/journal.pone.0153093. eCollection 2016.
The specific molecular mechanisms involved in somatic reprogramming remain unidentified. Removal of the oocyte genome is one of the primary causes of developmental failure in cloned embryos, whereas intact oocyte shows stronger reprogramming capability than enucleated oocyte. To identify the reason for the low efficiency of cloning and elucidate the mechanisms involved in somatic reprogramming by the oocyte nucleus, we injected pig cumulus cells into 539 intact MII oocytes and 461 enucleated MII oocytes. Following activation, 260 polyploidy embryos developed to the blastocyst stage whereas only 93 traditionally cloned embryos (48.2% vs. 20.2%, P < 0.01) reached blastocyst stage. Blastocysts generated from intact oocytes also had more cells than those generated from enucleated oocytes (60.70 vs. 46.65, P < 0.01). To identify the genes that contribute to this phenomenon, two early embryos in 2-cell and 4-cell stages were collected for single-cell RNA sequencing. The two kinds of embryos were found to have dramatically different transcriptome profiles. Intact oocyte nuclear transfer embryos showed 1,738 transcripts that were up-regulated relative to enucleated cloned embryos at the 2-cell stage and 728 transcripts that were down-regulated (|log2Ratio| ≥ 5). They showed 2,941 transcripts that were up-regulated during the 4-cell stage and 1,682 that were down-regulated (|log2Ratio| ≥ 5). The most significantly enriched gene ontology categories were those involved in the regulation of binding, catalytic activity, and molecular transducer activity. Other genes that were notably up-regulated and expressed in intact oocyte nuclear transfer embryos were metabolic process. This study provides a comprehensive profile of the differences in gene expression between intact oocyte nuclear transfer embryos and traditional nuclear transfer embryos. This work thus paves the way for further research on the mechanisms underlying somatic reprogramming by oocytes.
体细胞重编程所涉及的具体分子机制仍不清楚。去除卵母细胞基因组是克隆胚胎发育失败的主要原因之一,而完整的卵母细胞比去核卵母细胞具有更强的重编程能力。为了确定克隆效率低下的原因并阐明卵母细胞核介导的体细胞重编程机制,我们将猪卵丘细胞注入539个完整的MII期卵母细胞和461个去核的MII期卵母细胞中。激活后,260个多倍体胚胎发育到囊胚阶段,而只有93个传统克隆胚胎(48.2%对20.2%,P<0.01)达到囊胚阶段。完整卵母细胞产生的囊胚也比去核卵母细胞产生的囊胚有更多的细胞(60.70对46.65,P<0.01)。为了鉴定导致这种现象的基因,收集了处于2细胞和4细胞阶段的两个早期胚胎进行单细胞RNA测序。发现这两种胚胎具有显著不同的转录组图谱。完整卵母细胞核移植胚胎在2细胞阶段相对于去核克隆胚胎有1738个转录本上调,728个转录本下调(|log2Ratio|≥5)。在4细胞阶段,它们有2941个转录本上调,1682个转录本下调(|log2Ratio|≥5)。最显著富集的基因本体类别是那些参与结合、催化活性和分子转导活性调节的类别。在完整卵母细胞核移植胚胎中显著上调并表达的其他基因是代谢过程。本研究全面描述了完整卵母细胞核移植胚胎与传统核移植胚胎之间基因表达的差异。因此,这项工作为进一步研究卵母细胞介导的体细胞重编程机制铺平了道路。