首页> 外文期刊>Physiologia plantarum >The 5-methyl-deoxy-cytidine (5mdC) localization to reveal in situ the dynamics of DNA methylation chromatin pattern in a variety of plant organ and tissue cells during development
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The 5-methyl-deoxy-cytidine (5mdC) localization to reveal in situ the dynamics of DNA methylation chromatin pattern in a variety of plant organ and tissue cells during development

机译:5-甲基-脱氧胞苷(5mdC)定位揭示了发育过程中各种植物器官和组织细胞中DNA甲基化染色质模式的动态变化

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DNA methylation of cytosine residues constitutes a prominent epigenetic modification of the chromatin fiber which is locked in a transcriptionally inactive conformation leading to gene silencing. Plant developmental processes, as differentiation and proliferation, are accompanied by chromatin remodeling and epigenetic reprogramming. Despite the increasing knowledge gained on the epigenetic mechanisms controlling plant developmental processes, the knowledge of the DNA methylation regulation during relevant developmental programs in flowering plants, such as gametogenesis or embryogenesis, is very limited. The analysis of global DNA methylation levels has been frequently conducted by high performance capillary electrophoresis, and more recently also by ELISA-based assays, which provided quantitative data of whole organs and tissues. Nevertheless, to investigate the DNA methylation dynamics during plant development in different cell types of the same organ, the analysis of spatial and temporal pattern of nuclear distribution of 5-methyl-deoxy-cytidine (5mdC) constitutes a potent approach. In this work, immunolocalization of 5mdC on sections and subsequent confocal laser microscopy analysis have been applied for in situ cellular analysis of a variety of plant cells, tissues and organs with different characteristics, e.g. hardness, heterogeneity, cell accessibility, tissue compactness, etc.; the results demonstrated the versatility and feasibility of the approach for different plant samples, and revealed defined DNA methylation nuclear patterns associated with differentiation and proliferation events of various plant cell types and developmental programs. Quantification of 5mdC immunofluorescence intensity by image analysis software also permitted to estimate differences in global DNA methylation levels among different cells types of the same organ during development.
机译:胞嘧啶残基的DNA甲基化构成了染色质纤维的显着表观遗传修饰,该修饰被锁定在转录失活的构象中,导致基因沉默。植物的发育过程,如分化和增殖,伴随着染色质重塑和表观遗传重编程。尽管在控制植物发育过程的表观遗传机制上获得了越来越多的知识,但是在开花植物的相关发育程序中,例如配子发生或胚发生的DNA甲基化调控的知识仍然非常有限。全局DNA甲基化水平的分析经常通过高性能毛细管电泳进行,最近也通过基于ELISA的分析进行,该分析提供了整个器官和组织的定量数据。然而,要研究植物发育过程中同一器官的不同细胞类型中的DNA甲基化动力学,分析5-甲基-脱氧胞苷(5mdC)的核分布的时空格局是一种有效的方法。在这项工作中,将5mdC在切片上进行免疫定位并随后进行共聚焦激光显微镜分析已用于原位细胞分析各种具有不同特性的植物细胞,组织和器官,例如硬度,异质性,细胞可及性,组织致密性等;结果表明该方法适用于不同植物样品的多功能性和可行性,并揭示了与各种植物细胞类型和发育程序的分化和增殖事件相关的确定的DNA甲基化核模式。通过图像分析软件对5mdC免疫荧光强度进行定量分析,还可以估计发育过程中同一器官的不同细胞类型之间的整体DNA甲基化水平的差异。

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