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A Simple Method for Visualization of Locus-Specific H4K20me1 Modifications in Living Caenorhabditis elegans Single Cells

机译:活的秀丽隐杆线虫单细胞中特定于基因座的H4K20me1修饰的可视化的简单方法

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摘要

Recently, advances in next-generation sequencing technologies have enabled genome-wide analyses of epigenetic modifications; however, it remains difficult to analyze the states of histone modifications at a single-cell resolution in living multicellular organisms because of the heterogeneity within cellular populations. Here we describe a simple method to visualize histone modifications on the specific sequence of target locus at a single-cell resolution in living Caenorhabditis elegans, by combining the LacO/LacI system and a genetically-encoded H4K20me1-specific probe, “mintbody”. We demonstrate that Venus-labeled mintbody and mTurquoise2-labeled LacI can co-localize on an artificial chromosome carrying both the target locus and LacO sequences, where H4K20me1 marks the target locus. We demonstrate that our visualization method can precisely detect H4K20me1 depositions on the gene sequences on the artificial chromosome, to which the dosage compensation complex binds to regulate sex determination. The degree of H4K20me1 deposition on the sequences on the artificial chromosome correlated strongly with sex, suggesting that, using the artificial chromosome, this method can reflect context-dependent changes of H4K20me1 on endogenous genomes. Furthermore, we demonstrate live imaging of H4K20me1 depositions on the artificial chromosome. Combined with ChIP assays, this mintbody-LacO/LacI visualization method will enable analysis of developmental and context-dependent alterations of locus-specific histone modifications in specific cells and elucidation of the underlying molecular mechanisms.
机译:最近,下一代测序技术的进步使得对表观遗传修饰的全基因组分析成为可能。然而,由于细胞群体内的异质性,在活多细胞生物中以单细胞分辨率分析组蛋白修饰的状态仍然很困难。在这里,我们描述了一种简单的方法,通过结合LacO / LacI系统和基因编码的H4K20me1特异性探针“薄荷体”,在活的秀丽隐杆线虫中以单细胞分辨率可视化目标基因座特定序列的组蛋白修饰。我们证明金星标记的薄荷体和mTurquoise2标记的LacI可以共定位在携带目标基因座和LacO序列的人工染色体上,其中H4K20me1标记目标基因座。我们证明了我们的可视化方法可以精确地检测H4K20me1在人工染色体上的基因序列上的沉积,剂量补偿复合物与该序列结合以调节性别决定。 H4K20me1在人工染色体上的序列上的沉积程度与性别密切相关,这表明,使用人工染色体,该方法可以反映内源基因组上H4K20me1的上下文相关变化。此外,我们展示了人工染色体上H4K20me1沉积的实时成像。结合ChIP分析,这种mintbody-LacO / LacI可视化方法将能够分析特定细胞中特定基因组蛋白修饰的发育和背景相关变化,并阐明其潜在的分子机制。

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