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拟南芥有性生殖过程中DNA甲基化的活细胞分析揭示了由非经典RdDM控制的背景和性别特异性动态变化。

Live-cell analysis of DNA methylation during sexual reproduction in Arabidopsis reveals context and sex-specific dynamics controlled by noncanonical RdDM.

作者信息

Ingouff Mathieu, Selles Benjamin, Michaud Caroline, Vu Thiet M, Berger Frédéric, Schorn Andrea J, Autran Daphné, Van Durme Matthias, Nowack Moritz K, Martienssen Robert A, Grimanelli Daniel

机构信息

Epigenetic Regulations and Seed Development, UMR232, Institut de Recherche pour le Développement (IRD), Université de Montpellier, 34394 Montpellier, France.

Gregor Mendel Institute, Austrian Academy of Sciences, Vienna BioCenter, 1030 Vienna, Austria.

出版信息

Genes Dev. 2017 Jan 1;31(1):72-83. doi: 10.1101/gad.289397.116. Epub 2017 Jan 23.

Abstract

Cytosine methylation is a key epigenetic mark in many organisms, important for both transcriptional control and genome integrity. While relatively stable during somatic growth, DNA methylation is reprogrammed genome-wide during mammalian reproduction. Reprogramming is essential for zygotic totipotency and to prevent transgenerational inheritance of epimutations. However, the extent of DNA methylation reprogramming in plants remains unclear. Here, we developed sensors reporting with single-cell resolution CG and non-CG methylation in Arabidopsis. Live imaging during reproduction revealed distinct and sex-specific dynamics for both contexts. We found that CHH methylation in the egg cell depends on DOMAINS REARRANGED METHYLASE 2 (DRM2) and RNA polymerase V (Pol V), two main actors of RNA-directed DNA methylation, but does not depend on Pol IV. Our sensors provide insight into global DNA methylation dynamics at the single-cell level with high temporal resolution and offer a powerful tool to track CG and non-CG methylation both during development and in response to environmental cues in all organisms with methylated DNA, as we illustrate in mouse embryonic stem cells.

摘要

胞嘧啶甲基化是许多生物中的一种关键表观遗传标记,对转录控制和基因组完整性都很重要。虽然在体细胞生长过程中相对稳定,但DNA甲基化在哺乳动物繁殖过程中会在全基因组范围内重新编程。重新编程对于合子全能性和防止表观突变的跨代遗传至关重要。然而,植物中DNA甲基化重新编程的程度仍不清楚。在这里,我们开发了能够在拟南芥中以单细胞分辨率报告CG和非CG甲基化的传感器。繁殖过程中的实时成像揭示了这两种情况下不同的、性别特异性的动态变化。我们发现卵细胞中的CHH甲基化依赖于结构域重排甲基转移酶2(DRM2)和RNA聚合酶V(Pol V),这是RNA指导的DNA甲基化的两个主要参与者,但不依赖于Pol IV。我们的传感器以高时间分辨率在单细胞水平上深入了解了全局DNA甲基化动态,并提供了一个强大的工具来追踪CG和非CG甲基化,无论是在发育过程中还是在所有具有甲基化DNA的生物体中对环境线索的响应,正如我们在小鼠胚胎干细胞中所展示的那样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f44/5287115/65a1f91e590f/72f01.jpg

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