Mandal Chanchal, Kim Sun Hwa, Chai Jin Choul, Oh Seon Mi, Lee Young Seek, Jung Kyoung Hwa, Chai Young Gyu
Department of Molecular and Life Science, Hanyang University, Ansan, Republic of Korea.
Institute of Natural Science and Technology, Hanyang University, Ansan, Republic of Korea.
PLoS One. 2016 Mar 1;11(3):e0149976. doi: 10.1371/journal.pone.0149976. eCollection 2016.
Fetal alcohol spectrum disorder is a collective term representing fetal abnormalities associated with maternal alcohol consumption. Prenatal alcohol exposure and related anomalies are well characterized, but the molecular mechanism behind this phenomenon is not well characterized. In this present study, our aim is to profile important genes that regulate cellular development during fetal development. Human embryonic carcinoma cells (NCCIT) are cultured to form embryoid bodies and then treated in the presence and absence of ethanol (50 mM). We employed RNA sequencing to profile differentially expressed genes in the ethanol-treated embryoid bodies from NCCIT vs. EB, NCCIT vs. EB+EtOH and EB vs. EB+EtOH data sets. A total of 632, 205 and 517 differentially expressed genes were identified from NCCIT vs. EB, NCCIT vs. EB+EtOH and EB vs. EB+EtOH, respectively. Functional annotation using bioinformatics tools reveal significant enrichment of differential cellular development and developmental disorders. Furthermore, a group of 42, 15 and 35 transcription factor-encoding genes are screened from all of the differentially expressed genes obtained from NCCIT vs. EB, NCCIT vs. EB+EtOH and EB vs. EB+EtOH, respectively. We validated relative gene expression levels of several transcription factors from these lists by quantitative real-time PCR. We hope that our study substantially contributes to the understanding of the molecular mechanism underlying the pathology of alcohol-mediated anomalies and ease further research.
胎儿酒精谱系障碍是一个统称,代表与母亲饮酒相关的胎儿异常情况。产前酒精暴露及其相关异常已得到充分表征,但这一现象背后的分子机制尚未完全明确。在本研究中,我们的目的是剖析在胎儿发育过程中调节细胞发育的重要基因。培养人胚胎癌细胞(NCCIT)以形成胚状体,然后在有和没有乙醇(50 mM)的情况下进行处理。我们利用RNA测序来分析在乙醇处理的NCCIT来源的胚状体与EB、NCCIT与EB+EtOH以及EB与EB+EtOH数据集中差异表达的基因。分别从NCCIT与EB、NCCIT与EB+EtOH以及EB与EB+EtOH中鉴定出总共632、205和517个差异表达基因。使用生物信息学工具进行功能注释揭示了细胞发育差异和发育障碍的显著富集。此外,分别从NCCIT与EB、NCCIT与EB+EtOH以及EB与EB+EtOH获得的所有差异表达基因中筛选出一组分别包含42、15和35个编码转录因子的基因。我们通过定量实时PCR验证了这些列表中几个转录因子的相对基因表达水平。我们希望我们的研究能极大地有助于理解酒精介导的异常病理学背后的分子机制,并促进进一步的研究。