Evidence map›Paper›PMID 30523148›Full record

ArticleThe EMBO journal2019

SUMOylation coordinates BERosome assembly in active DNA demethylation during cell differentiation.

Roland Steinacher, Zeinab Barekati, Petar Botev, Anna Kuśnierczyk, Geir Slupphaug, Primo Schär

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. Article
  9. SUMO and the DNA damage response.Biochemical Society transactions · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Protein sumoylation in normal and cancer stem cells.Frontiers in molecular biosciences · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 3 countries.

Roland SteinacherDepartment of Biomedicine, University of Basel, Basel, Switzerland roland.steinacher@unibas.ch primo.schaer@unibas.ch.
Zeinab BarekatiDepartment of Biomedicine, University of Basel, Basel, Switzerland.
Petar BotevInstitute of Molecular Biology, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Anna KuśnierczykDepartment of Cancer Research and Molecular Medicine, Proteomics and Metabolomics Core Facility, PROMEC, Norwegian University of Science and Technology, Trondheim, Norway.
Geir SlupphaugDepartment of Cancer Research and Molecular Medicine, Proteomics and Metabolomics Core Facility, PROMEC, Norwegian University of Science and Technology, Trondheim, Norway.
Primo SchärDepartment of Biomedicine, University of Basel, Basel, Switzerland roland.steinacher@unibas.ch primo.schaer@unibas.ch.ORCID 0000-0003-1843-6147
University of Basel · CHNorwegian University of Science and Technology · NOBulgarian Academy of Sciences · BG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During active DNA demethylation, 5-methylcytosine (5mC) is oxidized by TET proteins to 5-formyl-/5-carboxylcytosine (5fC/5caC) for replacement by unmethylated C by TDG-initiated DNA base excision repair (BER). Base excision generates fragile abasic sites (AP-sites) in DNA and has to be coordinated with subsequent repair steps to limit accumulation of genome destabilizing secondary DNA lesions. Here, we show that 5fC/5caC is generated at a high rate in genomes of differentiating mouse embryonic stem cells and that SUMOylation and the BER protein XRCC1 play critical roles in orchestrating TDG-initiated BER of these lesions. SUMOylation of XRCC1 facilitates physical interaction with TDG and promotes the assembly of a TDG-BER core complex. Within this TDG-BERosome, SUMO is transferred from XRCC1 and coupled to the SUMO acceptor lysine in TDG, promoting its dissociation while assuring the engagement of the BER machinery to complete demethylation. Although well-studied, the biological importance of TDG SUMOylation has remained obscure. Here, we demonstrate that SUMOylation of TDG suppresses DNA strand-break accumulation and toxicity to PARP inhibition in differentiating mESCs and is essential for neural lineage commitment.

Indexed as

DNA Demethylation5-MethylcytosineAnimalsCell DifferentiationCells, CulturedCytosineDNA RepairEmbryonic Stem CellsHumansMiceMultiprotein ComplexesProtein MultimerizationSumoylationX-ray Repair Cross Complementing Protein 15-carboxylcytosine5-MethylcytosineCytosineMultiprotein ComplexesX-ray Repair Cross Complementing Protein 1base excision repairDNA demethylationsmall ubiquitin‐like modifierstem cell differentiation

Identifiers

PMID30523148
PMCPMC6315294
OpenAlexW2905380570

What OpenQuestion holds

Textmetadata
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.