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Substrate deformation regulates DRM2-mediated DNA methylation in plants

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. Howeve...

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Autores principales: Fang, Jian, Leichter, Sarah M., Jiang, Jianjun, Biswal, Mahamaya, Lu, Jiuwei, Zhang, Zhi-Min, Ren, Wendan, Zhai, Jixian, Cui, Qiang, Zhong, Xuehua, Song, Jikui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172135/
https://www.ncbi.nlm.nih.gov/pubmed/34078593
http://dx.doi.org/10.1126/sciadv.abd9224
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author Fang, Jian
Leichter, Sarah M.
Jiang, Jianjun
Biswal, Mahamaya
Lu, Jiuwei
Zhang, Zhi-Min
Ren, Wendan
Zhai, Jixian
Cui, Qiang
Zhong, Xuehua
Song, Jikui
author_facet Fang, Jian
Leichter, Sarah M.
Jiang, Jianjun
Biswal, Mahamaya
Lu, Jiuwei
Zhang, Zhi-Min
Ren, Wendan
Zhai, Jixian
Cui, Qiang
Zhong, Xuehua
Song, Jikui
author_sort Fang, Jian
collection PubMed
description 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.
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spelling pubmed-81721352021-06-10 Substrate deformation regulates DRM2-mediated DNA methylation in plants Fang, Jian Leichter, Sarah M. Jiang, Jianjun Biswal, Mahamaya Lu, Jiuwei Zhang, Zhi-Min Ren, Wendan Zhai, Jixian Cui, Qiang Zhong, Xuehua Song, Jikui Sci Adv Research Articles 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. American Association for the Advancement of Science 2021-06-02 /pmc/articles/PMC8172135/ /pubmed/34078593 http://dx.doi.org/10.1126/sciadv.abd9224 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Fang, Jian
Leichter, Sarah M.
Jiang, Jianjun
Biswal, Mahamaya
Lu, Jiuwei
Zhang, Zhi-Min
Ren, Wendan
Zhai, Jixian
Cui, Qiang
Zhong, Xuehua
Song, Jikui
Substrate deformation regulates DRM2-mediated DNA methylation in plants
title Substrate deformation regulates DRM2-mediated DNA methylation in plants
title_full Substrate deformation regulates DRM2-mediated DNA methylation in plants
title_fullStr Substrate deformation regulates DRM2-mediated DNA methylation in plants
title_full_unstemmed Substrate deformation regulates DRM2-mediated DNA methylation in plants
title_short Substrate deformation regulates DRM2-mediated DNA methylation in plants
title_sort substrate deformation regulates drm2-mediated dna methylation in plants
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172135/
https://www.ncbi.nlm.nih.gov/pubmed/34078593
http://dx.doi.org/10.1126/sciadv.abd9224
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