The DNA methylation–demethylation balance prevents development of multiple megaspore mother cells in Arabidopsis

Ting Jiang, Lei Li, Qianqian Hu, Xianyu Kuang, Lei Zhang, Wenjie Zeng, Daisuke Miki, Binglian Zheng
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Abstract

Female gametophyte development initiates from the megaspore mother cell (MMC), and only one somatic cell develops into an MMC. Here, we report that the balance between DNA methylation and demethylation ensures the maintenance of a single MMC in Arabidopsis (Arabidopsis thaliana). Surprisingly, a decrease or an increase of all three DNA methylation types (mCG, mCHG, and mCHH) caused abnormal enlargement of MMC-like cells and re-balancing DNA methylation rescued the enlarged MMC-like cellsin the mutants of regulators for DNA methylation and demethylation.. Systematic quantification of DNA methylation at the single-cell level demonstrated that mCHH levels begin to decrease from the central precursor MMC, preceding expression of the MMC marker KNUCKLES(KNU). Disrupting the regulation of DNA methylation caused the mCHH levels to become similar in the MMC and its neighboring cells, and these neighbors usually developed into MMC-like cells. Levels of the de novo DNA methyltransferase DOMAINS REARRANGED METHYLTRANSFERASE2 (DRM2) in the precursor MMC decreased before KNU expression, but the levels of the DNA glycosylase DEMETER decreased after KNU expression. Re-introduction of DRM2 or knockdown of DEMETER specifically in neighboring cells rescued the defects in drm1 drm2 double mutants. Collectively, our findings demonstrate that the balance of DNA methylation, rather than total methylation levels, facilitates maintenance of a single MMC.
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DNA甲基化-去甲基化平衡阻止了拟南芥中多个大孢子母细胞的发育
雌配子体发育始于大孢子母细胞(MMC),只有一个体细胞发育成MMC。在这里,我们报道了DNA甲基化和去甲基化之间的平衡确保了拟南芥(拟南芥)中单个MMC的维持。令人惊讶的是,所有三种DNA甲基化类型(mCG、mCHG和mCHH)的减少或增加都会导致mmc样细胞的异常增大,而在DNA甲基化和去甲基化调节因子突变体中,重新平衡DNA甲基化可以挽救增大的mmc样细胞。单细胞水平的DNA甲基化系统量化表明,在MMC标记KNUCKLES(KNU)表达之前,mCHH水平从中央前体MMC开始下降。破坏DNA甲基化的调节导致MMC及其邻近细胞中的mCHH水平变得相似,这些邻近细胞通常发育成MMC样细胞。在KNU表达前,前体MMC中从头DNA甲基转移酶域重排甲基转移酶e2 (DRM2)水平下降,但在KNU表达后,DNA糖基酶DEMETER水平下降。重新引入DRM2或在邻近细胞中特异性敲除DEMETER可挽救drm1和DRM2双突变体的缺陷。总的来说,我们的研究结果表明,DNA甲基化的平衡,而不是总甲基化水平,促进了单个MMC的维持。
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