Evidence map›Paper›PMID 35790763›Full record

ArticleNature communications2022

Mechanistic basis for maintenance of CHG DNA methylation in plants.

Jian Fang, Jianjun Jiang, Sarah M Leichter, Jie Liu, Mahamaya Biswal, Nelli Khudaverdyan, Xuehua Zhong, Jikui Song

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
13.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
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  3. Linking cellular metabolism to chromatin modifications in plants.Journal of integrative plant biology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Jian Fang *Department of Biochemistry, University of California, Riverside, CA, 92521, USA.ORCID 0000-0002-8652-1768
Jianjun Jiang *Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Sarah M Leichter *Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI, 53706, USA.ORCID 0000-0001-7572-3375
Jie LiuWisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, WI, 53715, USA.ORCID 0000-0002-1129-9584
Mahamaya BiswalDepartment of Biochemistry, University of California, Riverside, CA, 92521, USA.
Nelli KhudaverdyanDepartment of Biochemistry, University of California, Riverside, CA, 92521, USA.
Xuehua ZhongLaboratory of Genetics, University of Wisconsin-Madison, Madison, WI, 53706, USA. xuehua.zhong@wisc.edu.ORCID 0000-0002-2350-0046
Jikui SongDepartment of Biochemistry, University of California, Riverside, CA, 92521, USA. jikui.song@ucr.edu.ORCID 0000-0002-4958-1032
University of California, Riverside · USUniversity of Wisconsin–Madison · US

Funding

User Training and OutreachP30GM124165 · NIGMS · CORNELL UNIVERSITY · PI Nozomi Ando, J Christopher Fromme · 2018 to 2026
$34.2M
BIOTECHNOLOGY TRAINING PROGRAMT32GM008349 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FOX, BRIAN G · 1989 to 2019
$22.5M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007133 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PERNA, NICOLE T · 1985 to 2023
$16.5M
Mechanistic Insights into Mammalian DNA MethylationR35GM119721 · NIGMS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI Jikui Song · 2016 to 2026
$5.3M
Uncovering the epigenetic codes for genome integrity, developmental and environmental interaction.R35GM124806 · NIGMS · WASHINGTON UNIVERSITY · PI XUEHUA ZHONG · 2017 to 2026
$4.2M
Mechanistic Insights into flavivirus NS5-mediated STAT2 SuppressionR01AI153419 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI HAI, RONG · 2021 to 2025
$1.9M
Mechanistic understanding and inhibition of Zika NS5 proteinR21AI147057 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI HAI, RONG, SONG, JIKUI · 2019 to 2020
$739k
NIAID NIH HHS R01 AI153419NIAID NIH HHS R21 AI147057NIGMS NIH HHS P30 GM124165NIGMS NIH HHS R35 GM119721NIGMS NIH HHS R35 GM124806NIGMS NIH HHS T32 GM007133NIGMS NIH HHS T32 GM008349
6 · The paper itself

Abstract

DNA methylation is an evolutionarily conserved epigenetic mechanism essential for transposon silencing and heterochromatin assembly. In plants, DNA methylation widely occurs in the CG, CHG, and CHH (H = A, C, or T) contexts, with the maintenance of CHG methylation mediated by CMT3 chromomethylase. However, how CMT3 interacts with the chromatin environment for faithful maintenance of CHG methylation is unclear. Here we report structure-function characterization of the H3K9me2-directed maintenance of CHG methylation by CMT3 and its Zea mays ortholog ZMET2. Base-specific interactions and DNA deformation coordinately underpin the substrate specificity of CMT3 and ZMET2, while a bivalent readout of H3K9me2 and H3K18 allosterically stimulates substrate binding. Disruption of the interaction with DNA or H3K9me2/H3K18 led to loss of CMT3/ZMET2 activity in vitro and impairment of genome-wide CHG methylation in vivo. Together, our study uncovers how the intricate interplay of CMT3, repressive histone marks, and DNA sequence mediates heterochromatic CHG methylation.

Indexed as

DNA MethylationEpigenesis, GeneticZea mays

Identifiers

PMID35790763
PMCPMC9256654
OpenAlexW4284673223

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.