Evidence map›Paper›PMID 31363048›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Histone acetylation recruits the SWR1 complex to regulate active DNA demethylation in

Wen-Feng Nie, Mingguang Lei, Mingxuan Zhang, Kai Tang, Huan Huang, Cuijun Zhang, Daisuke Miki, Pan Liu, Yu Yang, Xingang Wang and 13 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
–field-weighted citation impact
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

49 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. IMPACTS OF DNA METHYLATION ON H2A.Z DEPOSITION AND NUCLEOSOME STABILITY.bioRxiv : the preprint server for biology · 2025
    Article
  8. Review
  9. Article
  10. Epigenetics in the modern era of crop improvements.Science China. Life sciences · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Roles of methyl-CpG-binding-domain (MBD) protiens in regulation of biological processes in plants.Physiology and molecular biology of plants : an international journal of functional plant biology · 2025
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Article
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

23 authors.

Wen-Feng NieShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Mingguang LeiShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Mingxuan ZhangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Kai TangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Huan HuangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Cuijun ZhangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Daisuke MikiShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Pan LiuShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Yu YangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Xingang WangDepartment of Horticulture & Landscape Architecture, Purdue University, West Lafayette, IN 47906.
Heng ZhangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Zhaobo LangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Na LiuInstitute of Vegetable Science, Zhejiang Academy of Agricultural Science, 310021 Hangzhou, China.
Xuechen XuDepartment of Horticulture, Zhejiang University, 310058 Hangzhou, China.
Ramesh YelagandulaGregor Mendel Institute, Austrian Academy of Sciences, 1030 Vienna, Austria.
Huiming ZhangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Zhidan WangShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Xiaoqiang ChaiShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Andrea AndreucciDepartment of Biology, University of Pisa, 56126 Pisa, Italy.
Jing-Quan YuDepartment of Horticulture, Zhejiang University, 310058 Hangzhou, China.
Frederic BergerGregor Mendel Institute, Austrian Academy of Sciences, 1030 Vienna, Austria.
Rosa Lozano-DuranShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China.
Jian-Kang ZhuShanghai Center for Plant Stress Biology, Center of Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, 201602 Shanghai, China; zhu132@purdue.edu.ORCID 0000-0001-5134-731X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Active DNA demethylation is critical for controlling the DNA methylomes in plants and mammals. However, little is known about how DNA demethylases are recruited to target loci, and the involvement of chromatin marks in this process. Here, we identify 2 components of the SWR1 chromatin-remodeling complex, PIE1 and ARP6, as required for ROS1-mediated DNA demethylation, and discover 2 SWR1-associated bromodomain-containing proteins, AtMBD9 and nuclear protein X1 (NPX1). AtMBD9 and NPX1 recognize histone acetylation marks established by increased DNA methylation 1 (IDM1), a known regulator of DNA demethylation, redundantly facilitating H2A.Z deposition at IDM1 target loci. We show that at some genomic regions, H2A.Z and DNA methylation marks coexist, and H2A.Z physically interacts with ROS1 to regulate DNA demethylation and antisilencing. Our results unveil a mechanism through which DNA demethylases can be recruited to specific target loci exhibiting particular histone marks, providing a conceptual framework to understand how chromatin marks regulate DNA demethylation.

Indexed as

DNA DemethylationAcetylationArabidopsisArabidopsis ProteinsChromatinGene SilencingHistonesModels, BiologicalMultiprotein ComplexesMutationProtein BindingProtein SubunitsArabidopsis ProteinsChromatinHistonesMultiprotein ComplexesProtein Subunitsbromodomainchromatin remodelingDNA demethylation pathwaygene silencinghistone variant

Identifiers

PMID31363048
PMCPMC6697875

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.