Evidence map›Paper›PMID 29394246›Full record

ArticlePLoS genetics2018

Nuclear re-localization of Dicer in primary mouse embryonic fibroblast nuclei following DNA damage.

Kaspar Burger, Monika Gullerova

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  5. Nono induces Gadd45b to mediate DNA repair.Life science alliance · 2024
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  17. Rare GermlineFrontiers in endocrinology · 2020
    Article
  18. Article
  19. Article
  20. Review
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

2 authors at 1 institution in 1 country.

Kaspar BurgerSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-0587-9782
Monika GullerovaSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-4512-2779
University of Oxford · GB

Funding

Cancer Research UK 24866Medical Research Council MR/K006606/1
6 · The paper itself

Abstract

Dicer is a key component of RNA interference (RNAi) and well-known for its role in biogenesis of micro (mi)RNA in the cytoplasm. Increasing evidence suggests that mammalian Dicer is also present and active in the nucleus. We have previously shown that phosphorylated human Dicer associates with chromatin in response to DNA damage and processes double-stranded (ds)RNA in the nucleus. However, a recent study by Much et al. investigated endogenously tagged HA-Dicer both in primary mouse embryonic fibroblasts (PMEFs) as well as adult homozygous viable and fertile HA-Dicer mice under physiological conditions and concluded that murine Dicer is exclusively cytoplasmic. The authors challenged several findings, reporting functions of Dicer in mammalian nuclei. We have re-investigated this issue by applying subcellular fractionation, super-resolution microscopy followed by 3D reconstitution, and phospho-Dicer-specific antibodies using the same HA-Dicer PMEF cell line. Our data show that a small fraction of the murine HA-Dicer pool, approximately 5%, localises in the nucleus and is phosphorylated upon DNA damage. We propose that Dicer localisation is dynamic and not exclusively cytoplasmic, particularly in cells exposed to DNA damage.

Indexed as

Active Transport, Cell NucleusAnimalsCell NucleusCells, CulturedDEAD-box RNA HelicasesDNA DamageEmbryo, MammalianFemaleFibroblastsGene Knockout TechniquesHEK293 CellsHumansMiceProtein TransportRibonuclease IIIDEAD-box RNA HelicasesDicer1 protein, mouseRibonuclease III

Identifiers

PMID29394246
PMCPMC5812656
OpenAlexW2785906793

What OpenQuestion holds

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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.