Evidence map›Paper›PMID 27577095›Full record

ArticleJournal of cell science2016

Drosophila sensory cilia lacking MKS proteins exhibit striking defects in development but only subtle defects in adults.

Metta B Pratt, Joshua S Titlow, Ilan Davis, Amy R Barker, Helen R Dawe, Jordan W Raff, Helio Roque

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. From mesenchymal niches to engineeredMaterials today. Bio · 2022
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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

7 authors at 3 institutions in 1 country.

Metta B PrattThe Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.ORCID 0000-0001-5296-1370
Joshua S TitlowDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Ilan DavisDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Amy R BarkerCentre for Microvascular Research, William Harvey Research Institute, Queen Mary University of London, London EC1M 6BQ, UK.
Helen R DaweBiosciences, College of Life and Environmental Sciences, University of Exeter, Exeter EX4 4QD, UK.
Jordan W RaffThe Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK jordan.raff@path.ox.ac.uk helio.roque@path.ox.ac.uk.ORCID 0000-0002-4689-1297
Helio RoqueThe Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK jordan.raff@path.ox.ac.uk helio.roque@path.ox.ac.uk.ORCID 0000-0002-5930-1989
University of Oxford · GBQueen Mary University of London · GBUniversity of Exeter · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council G1001644Wellcome Trust 091911Wellcome Trust 096144Wellcome Trust 104575
6 · The paper itself

Abstract

Cilia are conserved organelles that have important motility, sensory and signalling roles. The transition zone (TZ) at the base of the cilium is crucial for cilia function, and defects in several TZ proteins are associated with human congenital ciliopathies such as nephronophthisis (NPHP) and Meckel-Gruber syndrome (MKS). In several species, MKS and NPHP proteins form separate complexes that cooperate with Cep290 to assemble the TZ, but flies seem to lack core components of the NPHP module. We show that MKS proteins in flies are spatially separated from Cep290 at the TZ, and that flies mutant for individual MKS genes fail to recruit other MKS proteins to the TZ, whereas Cep290 seems to be recruited normally. Although there are abnormalities in microtubule and membrane organisation in developing MKS mutant cilia, these defects are less apparent in adults, where sensory cilia and sperm flagella seem to function quite normally. Thus, localising MKS proteins to the cilium or flagellum is not essential for viability or fertility in flies.

Indexed as

AgingAnimalsAxonemeBehavior, AnimalCiliaDrosophila melanogasterDrosophila ProteinsFlagellaMaleMechanoreceptorsMembrane ProteinsMutationProtein TransportSense OrgansSpermatocytesTestisDrosophila ProteinsMembrane ProteinsCiliogenesisMKS moduleSensory ciliaTransition zone

Identifiers

PMID27577095
PMCPMC5087661
OpenAlexW2951848036

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.