Evidence map›Paper›PMID 26358956›Full record

ReviewEMBO reports2015

New frontiers: discovering cilia-independent functions of cilia proteins.

Anastassiia Vertii, Alison Bright, Benedicte Delaval, Heidi Hehnly, Stephen Doxsey

Abstract readReview
In one paragraph

Review in EMBO reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
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

40 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Uncovering cilia function in glial development.Annals of human genetics · 2024
    Review
  9. Article
  10. Article
  11. PCD Genes-From Patients to Model Organisms and Back to Humans.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Primary Cilia Formation Does Not Rely on WNT/β-Catenin Signaling.Frontiers in cell and developmental biology · 2021
    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

5 authors.

Anastassiia VertiiProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Alison BrightProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Benedicte DelavalCRBM - CNRS Université de Montpellier, Montpellier, France.
Heidi HehnlyDepartment of Cell and Developmental Biology, SUNY Upstate Medical University, Syracuse, NY, USA HehnlyH@upstate.edu Stephen.Doxsey@umassmed.edu.
Stephen DoxseyProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA HehnlyH@upstate.edu Stephen.Doxsey@umassmed.edu.

Funding

Mitotic functions of cilia proteinsR01GM051994 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI DOXSEY, STEPHEN J · 1995 to 2014
$4.3M
Mother Centriole Appendages Regulate the AMIS Compartment and Cilogenesis.R00GM107355 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI HEHNLY, HEIDI · 2015 to 2017
$723k
Centrosome and mitotic functions of ciliary proteinsR56GM051994 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI DOXSEY, STEPHEN J · 2009 to 2009
$375k
Mother Centriole Appendages Regulate the AMIS Compartment and Cilogenesis.K99GM107355 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HEHNLY, HEIDI · 2013 to 2014
$171k
NIGMS NIH HHS GM 051994NIGMS NIH HHS K99 GM107355NIGMS NIH HHS K99GM107355NIGMS NIH HHS R00 GM107355NIGMS NIH HHS R01 GM051994NIGMS NIH HHS R56 GM051994
6 · The paper itself

Abstract

In most vertebrates, mitotic spindles and primary cilia arise from a common origin, the centrosome. In non-cycling cells, the centrosome is the template for primary cilia assembly and, thus, is crucial for their associated sensory and signaling functions. During mitosis, the duplicated centrosomes mature into spindle poles, which orchestrate mitotic spindle assembly, chromosome segregation, and orientation of the cell division axis. Intriguingly, both cilia and spindle poles are centrosome-based, functionally distinct structures that require the action of microtubule-mediated, motor-driven transport for their assembly. Cilia proteins have been found at non-cilia sites, where they have distinct functions, illustrating a diverse and growing list of cellular processes and structures that utilize cilia proteins for crucial functions. In this review, we discuss cilia-independent functions of cilia proteins and re-evaluate their potential contributions to "cilia" disorders.

Indexed as

AnimalsCentrosomeChromosome SegregationCiliaHeLa CellsHumansMicrotubulesMitosisProteinsSpindle ApparatusProteinsCentrosomeCiliaCiliopathiesIFTMTOC

Identifiers

PMID26358956
PMCPMC4766453

What OpenQuestion holds

Textmetadata
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.