Evidence map›Paper›PMID 28179500›Full record

ArticleOpen biology2017

Ninein is essential for apico-basal microtubule formation and CLIP-170 facilitates its redeployment to non-centrosomal microtubule organizing centres.

Deborah A Goldspink, Chris Rookyard, Benjamin J Tyrrell, Jonathan Gadsby, James Perkins, Elizabeth K Lund, Niels Galjart, Paul Thomas, Tom Wileman, Mette M Mogensen

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Mechanisms of cortical microtubule organization in epidermal keratinocytes.Cellular and molecular life sciences : CMLS · 2025
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  11. Review
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  18. Microtubule Anchoring: Attaching Dynamic Polymers to Cellular Structures.Frontiers in cell and developmental biology · 2022
    Review
  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

10 authors at 2 institutions in 2 countries.

Deborah A GoldspinkSchool of Biological Sciences, University of East Anglia, Norwich, UK.
Chris RookyardSchool of Computing Science, University of East Anglia, Norwich, UK.
Benjamin J TyrrellSchool of Biological Sciences, University of East Anglia, Norwich, UK.
Jonathan GadsbySchool of Biological Sciences, University of East Anglia, Norwich, UK.ORCID 0000-0001-7986-4917
James PerkinsSchool of Biological Sciences, University of East Anglia, Norwich, UK.
Elizabeth K LundSchool of Biological Sciences, University of East Anglia, Norwich, UK.
Niels GaljartDepartment of Cell Biology and Genetics, Erasmus MC, Rotterdam, The Netherlands.
Paul ThomasSchool of Biological Sciences, University of East Anglia, Norwich, UK.
Tom WilemanMedical School, University of East Anglia, Norwich, UK.
Mette M MogensenSchool of Biological Sciences, University of East Anglia, Norwich, UK m.mogensen@uea.ac.uk.ORCID 0000-0002-8965-1592
University of East Anglia · GBErasmus MC · NL

Funding

Biotechnology and Biological Sciences Research Council BB/J009040/1
6 · The paper itself

Abstract

Differentiation of columnar epithelial cells involves a dramatic reorganization of the microtubules (MTs) and centrosomal components into an apico-basal array no longer anchored at the centrosome. Instead, the minus-ends of the MTs become anchored at apical non-centrosomal microtubule organizing centres (n-MTOCs). Formation of n-MTOCs is critical as they determine the spatial organization of MTs, which in turn influences cell shape and function. However, how they are formed is poorly understood. We have previously shown that the centrosomal anchoring protein ninein is released from the centrosome, moves in a microtubule-dependent manner and accumulates at n-MTOCs during epithelial differentiation. Here, we report using depletion and knockout (KO) approaches that ninein expression is essential for apico-basal array formation and epithelial elongation and that CLIP-170 is required for its redeployment to n-MTOCs. Functional inhibition also revealed that IQGAP1 and active Rac1 coordinate with CLIP-170 to facilitate microtubule plus-end cortical targeting and ninein redeployment. Intestinal tissue and

Indexed as

AnimalsCell DifferentiationCell LineCell PolarityCell ShapeCytoskeletal ProteinsDogsEpithelial CellsGene Knockout TechniquesHumansMadin Darby Canine Kidney CellsMiceMicrotubule-Associated ProteinsMicrotubule-Organizing CenterMicrotubulesNeoplasm Proteinscytoplasmic linker protein 170Cytoskeletal ProteinsMicrotubule-Associated ProteinsNeoplasm ProteinsCLIP-170IQGAP1microtubulesnineinnon-centrosomal MTOCsRac1

Identifiers

PMID28179500
PMCPMC5356440
OpenAlexW2584036604

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.