Evidence map›Paper›PMID 28642363›Full record

ArticleThe Journal of cell biology2017

Nuclear phosphorylated Dicer processes double-stranded RNA in response to DNA damage.

Kaspar Burger, Margarita Schlackow, Martin Potts, Svenja Hester, Shabaz Mohammed, Monika Gullerova

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

66 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
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  10. NEAT1 promotes genome stability via mGenes & development · 2024
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  13. Nono induces Gadd45b to mediate DNA repair.Life science alliance · 2024
    Article
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  15. Review
  16. Article
  17. Article
  18. Article
  19. MicroRNA biogenesis pathway alterations in aging.Extracellular vesicles and circulating nucleic acids · 2023
    Review
  20. Article

6 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Kaspar BurgerSir William Dunn School of Pathology, University of Oxford, Oxford, UK.
Margarita SchlackowSir William Dunn School of Pathology, University of Oxford, Oxford, UK.
Martin PottsCambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.ORCID 0000-0002-6738-0066
Svenja HesterSir William Dunn School of Pathology, University of Oxford, Oxford, UK.ORCID 0000-0003-0744-5216
Shabaz MohammedDepartment of Biochemistry, University of Oxford, Oxford, UK.ORCID 0000-0003-2640-9560
Monika GullerovaSir William Dunn School of Pathology, University of Oxford, Oxford, UK monika.gullerova@path.ox.ac.uk.ORCID 0000-0002-4512-2779
University of Oxford · GBUniversity of Cambridge · GB

Funding

Medical Research Council BVRXMJ00Medical Research Council MR/K006606/1
6 · The paper itself

Abstract

The endoribonuclease Dicer is a key component of the human RNA interference pathway and is known for its role in cytoplasmic microRNA production. Recent findings suggest that noncanonical Dicer generates small noncoding RNA to mediate the DNA damage response (DDR). Here, we show that human Dicer is phosphorylated in the platform-Piwi/Argonaute/Zwille-connector helix cassette (S1016) upon induction of DNA damage. Phosphorylated Dicer (p-Dicer) accumulates in the nucleus and is recruited to DNA double-strand breaks. We further demonstrate that turnover of damage-induced nuclear, double-stranded (ds) RNA requires additional phosphorylation of carboxy-terminal Dicer residues (S1728 and S1852). DNA damage-induced nuclear Dicer accumulation is conserved in mammals. Dicer depletion causes endogenous DNA damage and delays the DDR by impaired recruitment of repair factors MDC1 and 53BP1. Collectively, we place Dicer within the context of the DDR by demonstrating a DNA damage-inducible phosphoswitch that causes localized processing of nuclear dsRNA by p-Dicer to promote DNA repair.

Indexed as

DNA Breaks, Double-StrandedDNA RepairA549 CellsAdaptor Proteins, Signal TransducingAnimalsArgonaute ProteinsCell Cycle ProteinsCell NucleusDEAD-box RNA HelicasesHEK293 CellsHumansMiceNuclear ProteinsNucleic Acid ConformationPhosphorylationRibonuclease IIIAdaptor Proteins, Signal TransducingArgonaute ProteinsCell Cycle ProteinsDEAD-box RNA HelicasesDICER1 protein, humanMDC1 protein, humanNuclear ProteinsPIWIL1 protein, humanRibonuclease IIIRNA, Double-StrandedTP53BP1 protein, humanTrans-ActivatorsTumor Suppressor p53-Binding Protein 1

Identifiers

PMID28642363
PMCPMC5551710
OpenAlexW2650005198

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.