Evidence map›Paper›PMID 34403482›Full record

ArticleNucleic acids research2021

AtHDA6 functions as an H3K18ac eraser to maintain pericentromeric CHG methylation in Arabidopsis thaliana.

Qianwen Wang, Xiucong Bao, Shengjie Chen, Huan Zhong, Yaqin Liu, Li Zhang, Yiji Xia, Friedrich Kragler, Ming Luo, Xiang David Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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

12 authors at 5 institutions in 3 countries.

Qianwen WangSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region.
Xiucong BaoDepartment of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong Special Administrative Region.
Shengjie ChenSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region.
Huan ZhongDepartment of Biology, Hong Kong Baptist University, Kowloon, Hong Kong Special Administrative Region.
Yaqin LiuSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region.
Li ZhangSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region.
Yiji XiaCenter for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region.ORCID 0000-0002-9543-8341
Friedrich KraglerMax-Planck-Institute of Molecular Plant Physiology, Wissenschaftspark Golm, Am Mühlenberg 1, 14476 Golm, Germany.ORCID 0000-0001-5308-2976
Ming LuoAgriculture and Biotechnology Research Center, Guangdong Provincial Key Laboratory of Applied Botany, Center of Economic Botany, Core Botanical Gardens, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China.
Xiang David LiDepartment of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong Special Administrative Region.ORCID 0000-0002-2797-4134
Hon-Ming LamSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region.ORCID 0000-0002-6673-8740
Shoudong ZhangSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region.ORCID 0000-0001-7332-7627
Chinese University of Hong Kong · HKHong Kong Baptist University · HKUniversity of Hong Kong · HKMax Planck Institute of Molecular Plant Physiology · DESouth China Botanical Garden · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pericentromeric DNA, consisting of high-copy-number tandem repeats and transposable elements, is normally silenced through DNA methylation and histone modifications to maintain chromosomal integrity and stability. Although histone deacetylase 6 (HDA6) has been known to participate in pericentromeric silencing, the mechanism is still yet unclear. Here, using whole genome bisulfite sequencing (WGBS) and chromatin immunoprecipitation-sequencing (ChIP-Seq), we mapped the genome-wide patterns of differential DNA methylation and histone H3 lysine 18 acetylation (H3K18ac) in wild-type and hda6 mutant strains. Results show pericentromeric CHG hypomethylation in hda6 mutants was mediated by DNA demethylases, not by DNA methyltransferases as previously thought. DNA demethylases can recognize H3K18ac mark and then be recruited to the chromatin. Using biochemical assays, we found that HDA6 could function as an 'eraser' enzyme for H3K18ac mark to prevent DNA demethylation. Oxford Nanopore Technology Direct RNA Sequencing (ONT DRS) also revealed that hda6 mutants with H3K18ac accumulation and CHG hypomethylation were shown to have transcriptionally active pericentromeric DNA.

Indexed as

Epigenesis, GeneticGene Expression Regulation, PlantHistone CodeAcetylationArabidopsisArabidopsis ProteinsCentromereChromatinDNA MethylationGene SilencingHistone DeacetylasesHistonesLysineMutationArabidopsis ProteinsAT5G63110 protein, ArabidopsisChromatinHistone DeacetylasesHistonesLysine

Identifiers

PMID34403482
PMCPMC8464031
OpenAlexW3193460999

What OpenQuestion holds

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Registered trials

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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.