Evidence map›Paper›PMID 20386732›Full record

ArticlePloS one2010

Perturbations of microRNA function in mouse dicer mutants produce retinal defects and lead to aberrant axon pathfinding at the optic chiasm.

Rita Pinter, Robert Hindges

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

51 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. MicroRNAs in the Mouse Developing Retina.International journal of molecular sciences · 2023
    Review
  6. miRNA: A Promising Therapeutic Target in Cancer.International journal of molecular sciences · 2022
    Review
  7. Review
  8. Review
  9. Retinal Degeneration Caused by Ago2 Disruption.Investigative ophthalmology & visual science · 2021
    Article
  10. Review
  11. MicroRNAs in Vascular Eye Diseases.International journal of molecular sciences · 2020
    Review
  12. Neurogenesis and Specification of Retinal Ganglion Cells.International journal of molecular sciences · 2020
    Review
  13. Review
  14. Wiring the Binocular Visual Pathways.International journal of molecular sciences · 2019
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

2 authors at 1 institution in 1 country.

Rita PinterMRC Centre for Developmental Neurobiology, King's College London, Guy's Campus, London, United Kingdom.
Robert Hindges
King's College London · GB

Funding

Medical Research Council G0601182Medical Research Council G0901899Wellcome TrustWellcome Trust 087883/Z/08/Z
6 · The paper itself

Abstract

backgroundDuring development axons encounter a variety of choice points where they have to make appropriate pathfinding decisions. The optic chiasm is a major decision point for retinal ganglion cell (RGC) axons en route to their target in order to ensure the correct wiring of the visual system. MicroRNAs (miRNAs) belong to the class of small non-coding RNA molecules and have been identified as important regulators of a variety of processes during embryonic development. However, their involvement in axon guidance decisions is less clear. METHODOLOGY/PRINCIPAL

findingsWe report here that the early loss of Dicer, an essential protein for the maturation of miRNAs, in all cells of the forming retina and optic chiasm leads to severe phenotypes of RGC axon pathfinding at the midline. Using a conditional deletion approach in mice, we find in homozygous Dicer mutants a marked increase of ipsilateral projections, RGC axons extending outside the optic chiasm, the formation of a secondary optic tract and a substantial number of RGC axons projecting aberrantly into the contralateral eye. In addition, the mutant mice display a microphthalmia phenotype.

conclusionsOur work demonstrates an important role of Dicer controlling the extension of RGC axons to the brain proper. It indicates that miRNAs are essential regulatory elements for mechanisms that ensure correct axon guidance decisions at the midline and thus have a central function in the establishment of circuitry during the development of the nervous system.

Indexed as

MutationAnimalsAxonsDEAD-box RNA HelicasesMiceMicroRNAsNeural PathwaysNeurogenesisOptic ChiasmRetinaRetinal Ganglion CellsRibonuclease IIIVisual PathwaysDEAD-box RNA HelicasesDicer1 protein, mouseMicroRNAsRibonuclease III

Identifiers

PMID20386732
PMCPMC2850387
OpenAlexW1980257381

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.