Evidence map›Paper›PMID 30357346›Full record

ArticleNucleic acids research2019

Methylation of UHRF1 by SET7 is essential for DNA double-strand break repair.

Ja Young Hahm, Ji-Young Kim, Jin Woo Park, Joo-Young Kang, Kee-Beom Kim, Se-Ryeon Kim, Hana Cho, Sang-Beom Seo

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

32 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. Article
  9. Review
  10. [Research Progress of Role and Mechanism of SETD7 in Tumor Occurrence 
and Progression].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. The UHRF protein family in epigenetics, development, and carcinogenesis.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2022
    Review
  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

8 authors at 1 institution in 1 country.

Ja Young HahmDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Republic of Korea.
Ji-Young KimDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Republic of Korea.
Jin Woo ParkDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Republic of Korea.
Joo-Young KangDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Republic of Korea.
Kee-Beom KimDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Republic of Korea.
Se-Ryeon KimDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Republic of Korea.
Hana ChoDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Republic of Korea.
Sang-Beom SeoDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Republic of Korea.
Chung-Ang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ubiquitin-like with PHD and RING finger domains 1 (UHRF1) is a key epigenetic regulator of DNA methylation maintenance and heterochromatin formation. The roles of UHRF1 in DNA damage repair also have been emphasized in recent years. However, the regulatory mechanism of UHRF1 remains elusive. In this study, we showed that UHRF1 is methylated by SET7 and demethylation is catalyzed by LSD1. In addition, methylation of UHRF1 is induced in response to DNA damage and its phosphorylation in S phase is a prerequisite for interaction with SET7. Furthermore, UHRF1 methylation catalyzes the conjugation of polyubiquitin chains to PCNA and promotes homologous recombination for DNA repair. SET7-mediated UHRF1 methylation is also shown to be essential for cell viability against DNA damage. Our data revealed the regulatory mechanism underlying the UHRF1 methylation status by SET7 and LSD1 in double-strand break repair pathway.

Indexed as

DNA Breaks, Double-StrandedCCAAT-Enhancer-Binding ProteinsDNA DamageDNA MethylationDNA RepairHeterochromatinHistone DemethylasesHistone-Lysine N-MethyltransferaseHumansPhosphorylationProliferating Cell Nuclear AntigenProtein BindingS PhaseUbiquitin-Protein LigasesCCAAT-Enhancer-Binding ProteinsHeterochromatinHistone DemethylasesHistone-Lysine N-MethyltransferaseKDM1A protein, humanProliferating Cell Nuclear AntigenSETD7 protein, humanUbiquitin-Protein LigasesUHRF1 protein, human

Identifiers

PMID30357346
PMCPMC6326791
OpenAlexW2898147552

What OpenQuestion holds

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LicenceCC BY-NC
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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.