Sun Xue-Jiao, Li Ming-Xing, Gong Chen-Zi, Chen Jing, Nasb Mohammad, Shah Sayed Zulfiqar Ali, Rehan Muhammad, Li Ya-Jie, Chen Hong
Department of Rehabilitation Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
PeerJ. 2020 Nov 13;8:e10075. doi: 10.7717/peerj.10075. eCollection 2020.
Human embryonic stem cells (hESC) have been an invaluable research tool to study motor neuron development and disorders. However, transcriptional regulation of multiple temporal stages from ESCs to spinal motor neurons (MNs) has not yet been fully elucidated. Thus, the goals of this study were to profile the time-course expression patterns of lncRNAs during MN differentiation of ESCs and to clarify the potential mechanisms of the lncRNAs that are related to MN differentiation.
We utilized our previous protocol which can harvest motor neuron in more than 90% purity from hESCs. Then, differentially expressed lncRNAs (DElncRNAs) and mRNAs (DEmRNAs) during MN differentiation were identified through RNA sequencing. Bioinformatic analyses were performed to assess potential biological functions of genes. We also performed qRT-PCR to validate the DElncRNAs and DEmRNAs.
A total of 441 lncRNAs and 1,068 mRNAs at day 6, 443 and 1,175 at day 12, and 338 lncRNAs and 68 mRNAs at day 18 were differentially expressed compared with day 0. Bioinformatic analyses identified that several key regulatory genes including POU5F1, TDGF1, SOX17, LEFTY2 and ZSCAN10, which involved in the regulation of embryonic development. We also predicted 283 target genes of DElncRNAs, in which 6 mRNAs were differentially expressed. Significant fold changes in lncRNAs (NCAM1-AS) and mRNAs (HOXA3) were confirmed by qRT-PCR. Then, through predicted overlapped miRNA verification, we constructed a lncRNA NCAM1-AS-miRNA-HOXA3 network.
人类胚胎干细胞(hESC)一直是研究运动神经元发育和疾病的宝贵研究工具。然而,从胚胎干细胞到脊髓运动神经元(MNs)多个时间阶段的转录调控尚未完全阐明。因此,本研究的目的是描绘胚胎干细胞向运动神经元分化过程中lncRNAs的时间进程表达模式,并阐明与运动神经元分化相关的lncRNAs的潜在机制。
我们利用之前的方案,该方案可以从人类胚胎干细胞中收获纯度超过90%的运动神经元。然后,通过RNA测序鉴定运动神经元分化过程中差异表达的lncRNAs(DElncRNAs)和mRNAs(DEmRNAs)。进行生物信息学分析以评估基因的潜在生物学功能。我们还进行了qRT-PCR以验证DElncRNAs和DEmRNAs。
与第0天相比,第6天共有441个lncRNAs和1068个mRNAs、第12天有443个lncRNAs和1175个mRNAs、第18天有338个lncRNAs和68个mRNAs差异表达。生物信息学分析确定了几个关键调控基因,包括参与胚胎发育调控的POU5F1、TDGF1、SOX17、LEFTY2和ZSCAN10。我们还预测了DElncRNAs的283个靶基因,其中6个mRNAs差异表达。通过qRT-PCR证实了lncRNAs(NCAM1-AS)和mRNAs(HOXA3)的显著倍数变化。然后,通过预测的重叠miRNA验证,我们构建了lncRNA NCAM1-AS-miRNA-HOXA3网络。