Mingqi Zhou, Alberto Riva, Marie-Pierre L. Gauthier, Michael P. Kladde, Robert J. Ferl, Anna-Lisa Paul
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To provide methylation data at single-molecule resolution, Flap-enabled next-generation capture (FENGC), a novel targeted multiplexed DNA capture and enrichment technique allowing cleavage at any specified sites, was applied to survey spaceflight-altered DNA methylation in genic regions of interest. The FENGC capture panel contained 108 targets ranging from 509 to 704 nt within the promoter or gene body regions of gene targets derived from spaceflight whole-genome data sets. In addition to genes with significant changes in expression and average methylation levels between spaceflight and ground control, targets with space-altered distributions of the proportion of methylated cytosines per molecule were identified. Moreover, trends of co-methylation of different cytosine contexts were exhibited in the same DNA molecules. We further identified significant DNA methylation changes in three previously biological process-unknown genes, and loss-of-function mutants of two of these genes (named as EMO1 and EMO2 for ELP2-regulated Methylation in Orbit 1 and 2) showed enhanced root growth rate. FENGC simplifies and reduces the cost of multiplexed, targeted, single-molecule profiling of methylation in plants, providing additional resolution along each DNA molecule that is not seen in population-based short-read data such as WGBS. This case study has revealed spaceflight-altered regional modification of cytosine methylation occurring within single DNA molecules of cell subpopulations, which were not identified by WGBS. The single-molecule survey by FENGC can lead to identification of novel functional genes. 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We further identified significant DNA methylation changes in three previously biological process-unknown genes, and loss-of-function mutants of two of these genes (named as EMO1 and EMO2 for ELP2-regulated Methylation in Orbit 1 and 2) showed enhanced root growth rate. FENGC simplifies and reduces the cost of multiplexed, targeted, single-molecule profiling of methylation in plants, providing additional resolution along each DNA molecule that is not seen in population-based short-read data such as WGBS. This case study has revealed spaceflight-altered regional modification of cytosine methylation occurring within single DNA molecules of cell subpopulations, which were not identified by WGBS. The single-molecule survey by FENGC can lead to identification of novel functional genes. 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引用次数: 0
摘要
国际空间站上的先进植物实验-04-表观遗传表达(APEX-04-EpEx)实验研究了拟南芥两个遗传品系(野生型Col-0和缺乏表观遗传调节因子延伸复合体亚基2(ELP2)的突变体elp2-5)中受空间飞行影响的胞嘧啶甲基化情况。全基因组亚硫酸氢盐测序(WGBS)发现了与太空飞行相关的不同甲基化差异,因此需要以单个分子的分辨率探索特定空间改变的甲基化,以关联太空飞行相关基因大区域的特定变化。迄今为止,针对植物基因组的多重靶向 DNA 甲基化测序工具仍然有限。为了提供单分子分辨率的甲基化数据,我们采用了一种新型的靶向多路复用 DNA 捕获和富集技术--Flap-enabled next-generation capture(FENGC),允许在任何指定位点进行裂解。FENGC 捕获面板包含 108 个靶点,范围从 509 nt 到 704 nt 不等,这些靶点位于太空飞行全基因组数据集中基因靶点的启动子或基因体区域。除了发现在太空飞行和地面对照之间表达和平均甲基化水平有显著变化的基因外,还发现了每个分子中甲基化胞嘧啶比例的分布在太空中发生变化的靶标。此外,在相同的 DNA 分子中,不同的胞嘧啶上下文呈现出共甲基化的趋势。我们进一步发现了三个以前在生物学过程中未知的基因发生了明显的DNA甲基化变化,其中两个基因的功能缺失突变体(分别被命名为EMO1和EMO2,代表ELP2-regulated Methylation in Orbit 1和ELP2)表现出更高的根生长速率。FENGC 简化并降低了植物甲基化的多路复用、靶向、单分子分析的成本,提供了基于群体的短读数数据(如 WGBS)所不具备的每个 DNA 分子的额外分辨率。该案例研究揭示了在细胞亚群的单个 DNA 分子中发生的胞嘧啶甲基化的区域性改变,而这些改变是 WGBS 无法识别的。利用 FENGC 进行单分子调查可以发现新的功能基因。新发现的EMO1和EMO2是根系生长调节因子,可能在表观遗传学上参与了植物对太空飞行的适应。
Single-molecule long-read methylation profiling reveals regional DNA methylation regulated by Elongator Complex Subunit 2 in Arabidopsis roots experiencing spaceflight
The Advanced Plant Experiment-04 - Epigenetic Expression (APEX-04-EpEx) experiment onboard the International Space Station examined the spaceflight-altered cytosine methylation in two genetic lines of Arabidopsis thaliana, wild-type Col-0 and the mutant elp2-5, which is deficient in an epigenetic regulator Elongator Complex Subunit 2 (ELP2). Whole-genome bisulfite sequencing (WGBS) revealed distinct spaceflight associated methylation differences, presenting the need to explore specific space-altered methylation at single-molecule resolution to associate specific changes over large regions of spaceflight related genes. To date, tools of multiplexed targeted DNA methylation sequencing remain limited for plant genomes. To provide methylation data at single-molecule resolution, Flap-enabled next-generation capture (FENGC), a novel targeted multiplexed DNA capture and enrichment technique allowing cleavage at any specified sites, was applied to survey spaceflight-altered DNA methylation in genic regions of interest. The FENGC capture panel contained 108 targets ranging from 509 to 704 nt within the promoter or gene body regions of gene targets derived from spaceflight whole-genome data sets. In addition to genes with significant changes in expression and average methylation levels between spaceflight and ground control, targets with space-altered distributions of the proportion of methylated cytosines per molecule were identified. Moreover, trends of co-methylation of different cytosine contexts were exhibited in the same DNA molecules. We further identified significant DNA methylation changes in three previously biological process-unknown genes, and loss-of-function mutants of two of these genes (named as EMO1 and EMO2 for ELP2-regulated Methylation in Orbit 1 and 2) showed enhanced root growth rate. FENGC simplifies and reduces the cost of multiplexed, targeted, single-molecule profiling of methylation in plants, providing additional resolution along each DNA molecule that is not seen in population-based short-read data such as WGBS. This case study has revealed spaceflight-altered regional modification of cytosine methylation occurring within single DNA molecules of cell subpopulations, which were not identified by WGBS. The single-molecule survey by FENGC can lead to identification of novel functional genes. The newly identified EMO1 and EMO2 are root growth regulators which may be epigenetically involved in plant adaptation to spaceflight.
期刊介绍:
Biology Direct serves the life science research community as an open access, peer-reviewed online journal, providing authors and readers with an alternative to the traditional model of peer review. Biology Direct considers original research articles, hypotheses, comments, discovery notes and reviews in subject areas currently identified as those most conducive to the open review approach, primarily those with a significant non-experimental component.