Evidence map›Paper›PMID 22595669›Full record

ArticleDevelopmental cell2012

IFT25 links the signal-dependent movement of Hedgehog components to intraflagellar transport.

Brian T Keady, Rajeev Samtani, Kimimasa Tobita, Maiko Tsuchya, Jovenal T San Agustin, John A Follit, Julie A Jonassen, Ramiah Subramanian, Cecilia W Lo, Gregory J Pazour

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 151 papers.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed
13.6field-weighted citation impact, top 1% 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

151 citing papers in PubMed, 221 citations in OpenAlex.

  1. Review
  2. Primary cilia and neural computation.Journal of biomedical science · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Ventral body wall closure: Mechanistic insights from mouse models and translation to human pathology.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Review
  9. Article
  10. Article
  11. Intraflagellar Transport (IFT) and Sperm Formation.Advances in experimental medicine and biology · 2025
    Review
  12. Article
  13. Article
  14. Cilia Structure and Function in Human Disease.Current opinion in endocrine and metabolic research · 2024
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. RABL2 promotes the outward transition zone passage of signaling proteins in cilia via ARL3.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article

91 more citing papers are in PubMed but not listed here.

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 1 country.

Brian T KeadyProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Rajeev Samtani
Kimimasa Tobita
Maiko Tsuchya
Jovenal T San Agustin
John A Follit
Julie A Jonassen
Ramiah Subramanian
Cecilia W Lo
Gregory J Pazour
University of Massachusetts Chan Medical School · USUniversity of Pittsburgh · US

Funding

PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
Intraflagellar Transport Proteins in MiceR01GM060992 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Gregory J Pazour · 2001 to 2026
$10.3M
Modeling the genetic basis for human congenital heart disease in miceU01HL098180 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LO, CECILIA W. · 2009 to 2014
$8.5M
NHLBI NIH HHS 5U01HL098180NHLBI NIH HHS U01 HL098180NIDDK NIH HHS DK32520NIDDK NIH HHS P30 DK032520NIGMS NIH HHS GM060992NIGMS NIH HHS R01 GM060992
6 · The paper itself

Abstract

The intraflagellar transport (IFT) system is required for building primary cilia, sensory organelles that cells use to respond to their environment. IFT particles are composed of about 20 proteins, and these proteins are highly conserved across ciliated species. IFT25, however, is absent from some ciliated organisms, suggesting that it may have a unique role distinct from ciliogenesis. Here, we generate an Ift25 null mouse and show that IFT25 is not required for ciliary assembly but is required for proper Hedgehog signaling, which in mammals occurs within cilia. Mutant mice die at birth with multiple phenotypes, indicative of Hedgehog signaling dysfunction. Cilia lacking IFT25 have defects in the signal-dependent transport of multiple Hedgehog components including Patched-1, Smoothened, and Gli2, and fail to activate the pathway upon stimulation. Thus, IFT function is not restricted to building cilia where signaling occurs, but also plays a separable role in signal transduction events.

Indexed as

AnimalsBiological TransportCell Culture TechniquesCiliaFlagellaGene Expression Regulation, DevelopmentalHedgehog ProteinsIntracellular Signaling Peptides and ProteinsKruppel-Like Transcription FactorsMiceMice, Inbred C57BLMice, KnockoutPatched-1 ReceptorPatched ReceptorsReceptors, Cell SurfaceReceptors, G-Protein-CoupledGli2 protein, mouseHedgehog ProteinsIFT25 protein, mouseIntracellular Signaling Peptides and ProteinsKruppel-Like Transcription FactorsPatched-1 ReceptorPatched ReceptorsPtch1 protein, mouseReceptors, Cell SurfaceReceptors, G-Protein-CoupledSmoothened ReceptorSmo protein, mouseZinc Finger Protein Gli2

Identifiers

PMID22595669
PMCPMC3366633
OpenAlexW1997628120

What OpenQuestion holds

Textmetadata
LicenceTDM
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.