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底物变形调控植物中 DRM2 介导的 DNA 甲基化。

Substrate deformation regulates DRM2-mediated DNA methylation in plants.

机构信息

Department of Biochemistry, University of California, Riverside, Riverside, CA 92521, USA.

Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI 53706, USA.

出版信息

Sci Adv. 2021 Jun 2;7(23). doi: 10.1126/sciadv.abd9224. Print 2021 Jun.

Abstract

DNA methylation is a major epigenetic mechanism critical for gene expression and genome stability. In plants, domains rearranged methyltransferase 2 (DRM2) preferentially mediates CHH (H = C, T, or A) methylation, a substrate specificity distinct from that of mammalian DNA methyltransferases. However, the underlying mechanism is unknown. Here, we report structure-function characterization of DRM2-mediated methylation. An arginine finger from the catalytic loop intercalates into the nontarget strand of DNA through the minor groove, inducing large DNA deformation that affects the substrate preference of DRM2. The target recognition domain stabilizes the enlarged major groove via shape complementarity rather than base-specific interactions, permitting substrate diversity. The engineered DRM2 C397R mutation introduces base-specific contacts with the +2-flanking guanine, thereby shifting the substrate specificity of DRM2 toward CHG DNA. Together, this study uncovers DNA deformation as a mechanism in regulating the specificity of DRM2 toward diverse CHH substrates and illustrates methylome complexity in plants.

摘要

DNA 甲基化是一种重要的表观遗传机制,对于基因表达和基因组稳定性至关重要。在植物中,结构域重排甲基转移酶 2(DRM2)优先介导 CHH(H = C、T 或 A)甲基化,其底物特异性与哺乳动物 DNA 甲基转移酶不同。然而,其潜在的机制尚不清楚。在这里,我们报告了 DRM2 介导的甲基化的结构-功能特征。来自催化环的精氨酸指通过小沟插入 DNA 的非靶链,引起大的 DNA 变形,从而影响 DRM2 的底物偏好性。靶标识别结构域通过形状互补而不是碱基特异性相互作用稳定扩大的主沟,从而允许底物多样性。工程化的 DRM2 C397R 突变与+2 侧翼鸟嘌呤形成碱基特异性接触,从而使 DRM2 的底物特异性向 CHG DNA 转移。总之,这项研究揭示了 DNA 变形作为调节 DRM2 对不同 CHH 底物特异性的机制,并说明了植物中甲基组的复杂性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b761/8172135/51984cf32301/abd9224-F1.jpg

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