Chowdhury Basudev, Seetharam Arun, Wang Zhiping, Liu Yunlong, Lossie Amy C, Thimmapuram Jyothi, Irudayaraj Joseph
Department of Biological Sciences, Purdue University, West Lafayette, IN, 47907, United States of America.
Bindley Biosciences Center, Discovery Park, Purdue University, West Lafayette IN, 47907, United States of America.
PLoS One. 2016 Jan 28;11(1):e0147514. doi: 10.1371/journal.pone.0147514. eCollection 2016.
Cells alter their gene expression in response to exposure to various environmental changes. Epigenetic mechanisms such as DNA methylation are believed to regulate the alterations in gene expression patterns. In vitro and in vivo studies have documented changes in cellular proliferation, cytoskeletal remodeling, signal transduction, bone mineralization and immune deficiency under the influence of microgravity conditions experienced in space. However microgravity induced changes in the epigenome have not been well characterized. In this study we have used Next-generation Sequencing (NGS) to profile ground-based "simulated" microgravity induced changes on DNA methylation (5-methylcytosine or 5mC), hydroxymethylation (5-hydroxymethylcytosine or 5hmC), and simultaneous gene expression in cultured human lymphoblastoid cells. Our results indicate that simulated microgravity induced alterations in the methylome (~60% of the differentially methylated regions or DMRs are hypomethylated and ~92% of the differentially hydroxymethylated regions or DHMRs are hyperhydroxymethylated). Simulated microgravity also induced differential expression in 370 transcripts that were associated with crucial biological processes such as oxidative stress response, carbohydrate metabolism and regulation of transcription. While we were not able to obtain any global trend correlating the changes of methylation/ hydroxylation with gene expression, we have been able to profile the simulated microgravity induced changes of 5mC over some of the differentially expressed genes that includes five genes undergoing differential methylation over their promoters and twenty five genes undergoing differential methylation over their gene-bodies. To the best of our knowledge, this is the first NGS-based study to profile epigenomic patterns induced by short time exposure of simulated microgravity and we believe that our findings can be a valuable resource for future explorations.
细胞会根据暴露于各种环境变化而改变其基因表达。诸如DNA甲基化等表观遗传机制被认为可调节基因表达模式的改变。体外和体内研究记录了在太空微重力条件影响下细胞增殖、细胞骨架重塑、信号转导、骨矿化和免疫缺陷方面的变化。然而,微重力诱导的表观基因组变化尚未得到充分表征。在本研究中,我们使用下一代测序(NGS)来分析地面“模拟”微重力对培养的人淋巴母细胞中DNA甲基化(5-甲基胞嘧啶或5mC)、羟甲基化(5-羟甲基胞嘧啶或5hmC)以及同时的基因表达所诱导的变化。我们的结果表明,模拟微重力诱导了甲基化组的改变(约60%的差异甲基化区域或DMRs发生低甲基化,约92%的差异羟甲基化区域或DHMRs发生高羟甲基化)。模拟微重力还诱导了370个转录本的差异表达,这些转录本与关键生物学过程如氧化应激反应、碳水化合物代谢和转录调控相关。虽然我们未能获得甲基化/羟化变化与基因表达相关的任何总体趋势,但我们能够分析模拟微重力在一些差异表达基因上诱导的5mC变化,其中包括五个在其启动子上发生差异甲基化的基因和二十五个在其基因体上发生差异甲基化的基因。据我们所知,这是第一项基于NGS的研究,用于分析短时间暴露于模拟微重力所诱导的表观基因组模式,我们相信我们的发现可为未来的探索提供宝贵资源。