Evidence map›Paper›PMID 28346477›Full record

ArticlePLoS genetics2017

Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear.

Andrew Forge, Ruth R Taylor, Sally J Dawson, Michael Lovett, Daniel J Jagger

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. The potassium channel KNature communications · 2025
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  11. Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

5 authors at 2 institutions in 1 country.

Andrew ForgeUCL Ear Institute, University College London, London, United Kingdom.ORCID 0000-0002-0995-0219
Ruth R TaylorUCL Ear Institute, University College London, London, United Kingdom.
Sally J DawsonUCL Ear Institute, University College London, London, United Kingdom.ORCID 0000-0002-4421-2043
Michael LovettNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Daniel J JaggerUCL Ear Institute, University College London, London, United Kingdom.
University College London · GBImperial College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M00659X/1Biotechnology and Biological Sciences Research Council BB/M019322/1
6 · The paper itself

Abstract

Behavioural anomalies suggesting an inner ear disorder were observed in a colony of transgenic mice. Affected animals were profoundly deaf. Severe hair bundle defects were identified in all outer and inner hair cells (OHC, IHC) in the cochlea and in hair cells of vestibular macular organs, but hair cells in cristae were essentially unaffected. Evidence suggested the disorder was likely due to gene disruption by a randomly inserted transgene construct. Whole-genome sequencing identified interruption of the SorCS2 (Sortilin-related VPS-10 domain containing protein) locus. Real-time-qPCR demonstrated disrupted expression of SorCS2 RNA in cochlear tissue from affected mice and this was confirmed by SorCS2 immuno-labelling. In all affected hair cells, stereocilia were shorter than normal, but abnormalities of bundle morphology and organisation differed between hair cell types. Bundles on OHC were grossly misshapen with significantly fewer stereocilia than normal. However, stereocilia were organised in rows of increasing height. Bundles on IHC contained significantly more stereocilia than normal with some longer stereocilia towards the centre, or with minimal height differentials. In early postnatal mice, kinocilia (primary cilia) of IHC and of OHC were initially located towards the lateral edge of the hair cell surface but often became surrounded by stereocilia as bundle shape and apical surface contour changed. In macular organs the kinocilium was positioned in the centre of the cell surface throughout maturation. There was disruption of the signalling pathway controlling intrinsic hair cell apical asymmetry. LGN and Gαi3 were largely absent, and atypical Protein Kinase C (aPKC) lost its asymmetric distribution. The results suggest that SorCS2 plays a role upstream of the intrinsic polarity pathway and that there are differences between hair cell types in the deployment of the machinery that generates a precisely organised hair bundle.

Indexed as

Gene Expression RegulationAge FactorsAnimalsHair Cells, Auditory, InnerHearing LossImmunohistochemistryMice, Inbred C57BLMice, KnockoutMice, TransgenicMicroscopy, ConfocalMicroscopy, Electron, ScanningNerve Tissue ProteinsOrgan of CortiReceptors, Cell SurfaceReverse Transcriptase Polymerase Chain ReactionStereociliaNerve Tissue ProteinsReceptors, Cell SurfaceSorCS2 protein, mouse

Identifiers

PMID28346477
PMCPMC5386298
OpenAlexW2600504948

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.