Evidence map›Paper›PMID 25728313›Full record

ArticleDevelopmental neurobiology2015

miR-181a/b control the assembly of visual circuitry by regulating retinal axon specification and growth.

Sabrina Carrella, Ylenia D'Agostino, Sara Barbato, Sabina P Huber-Reggi, Francesco G Salierno, Anna Manfredi, Stephan C F Neuhauss, Sandro Banfi, Ivan Conte

Open access · hybridAbstract read
In one paragraph

Article in Developmental neurobiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. MiRNA Regulatory Functions in Photoreceptors.Frontiers in cell and developmental biology · 2020
    Review
  11. Review
  12. Article
  13. PAR3-PAR6-atypical PKC polarity complex proteins in neuronal polarization.Cellular and molecular life sciences : CMLS · 2018
    Review
  14. Article
  15. 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

9 authors at 3 institutions in 2 countries.

Sabrina CarrellaTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, Pozzuoli (Naples), 80078, Italy.
Ylenia D'AgostinoTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, Pozzuoli (Naples), 80078, Italy.
Sara BarbatoTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, Pozzuoli (Naples), 80078, Italy.
Sabina P Huber-ReggiInstitute of Molecular Life Sciences, Division of Neurobiology, University of Zurich, Winterthurerstrasse 190, CH-8057, Zurich, Switzerland.
Francesco G SaliernoTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, Pozzuoli (Naples), 80078, Italy.
Anna ManfrediTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, Pozzuoli (Naples), 80078, Italy.
Stephan C F NeuhaussInstitute of Molecular Life Sciences, Division of Neurobiology, University of Zurich, Winterthurerstrasse 190, CH-8057, Zurich, Switzerland.
Sandro BanfiTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, Pozzuoli (Naples), 80078, Italy.
Ivan ConteTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, Pozzuoli (Naples), 80078, Italy.
Telethon Institute Of Genetics And Medicine · ITLife Science Zurich · CHInstitute of Genetics and Biophysics · IT

Funding

Telethon TGM11SB2
6 · The paper itself

Abstract

Connectivity and function of neuronal circuitry require the correct specification and growth of axons and dendrites. Here, we identify the microRNAs miR-181a and miR-181b as key regulators of retinal axon specification and growth. Loss of miR-181a/b in medaka fish (Oryzias latipes) failed to consolidate amacrine cell processes into axons and delayed the growth of retinal ganglion cell (RGC) axons. These alterations were accompanied by defects in visual connectivity and function. We demonstrated that miR-181a/b exert these actions through negative modulation of MAPK/ERK signaling that in turn leads to RhoA reduction and proper neuritogenesis in both amacrine cells and RGCs via local cytoskeletal rearrangement. Our results identify a new pathway for axon specification and growth unraveling a crucial role of miR-181a/b in the proper establishment of visual system connectivity and function.

Indexed as

Amacrine CellsAnimalsAnimals, Genetically ModifiedAxonsCell EnlargementCells, CulturedCytoskeletonFish ProteinsMAP Kinase Signaling SystemMicroRNAsOryziasRetinal Ganglion CellsrhoA GTP-Binding ProteinVision, OcularVisual PathwaysFish ProteinsMicroRNAsrhoA GTP-Binding Proteinaxon specificationMAPK signalingmiR-181amiR-181bretina

Identifiers

PMID25728313
PMCPMC5033011
OpenAlexW2010073033

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.