Evidence map›Paper›PMID 18691888›Full record

ArticleCurrent biology : CB2008

Costal2 functions as a kinesin-like protein in the hedgehog signal transduction pathway.

Shohreh F Farzan, Manuel Ascano, Stacey K Ogden, Matthieu Sanial, Amira Brigui, Anne Plessis, David J Robbins

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Signaling in the primary cilium through the lens of the Hedgehog pathway.Wiley interdisciplinary reviews. Developmental biology · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Genetic interaction screens identify a role for hedgehog signaling in Drosophila border cell migration.Developmental dynamics : an official publication of the American Association of Anatomists · 2013
    Article
  13. Article
  14. Review
  15. Article
  16. Unconventional functions of microtubule motors.Archives of biochemistry and biophysics · 2012
    Review
  17. Kinesin motors and primary cilia.Biochemical Society transactions · 2011
    Review
  18. Article
  19. Review
  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

7 authors at 2 institutions in 2 countries.

Shohreh F FarzanDepartment of Pharmacology and Toxicology, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.
Manuel Ascano
Stacey K Ogden
Matthieu Sanial
Amira Brigui
Anne Plessis
David J Robbins
Dartmouth College · USUniversité Paris Cité · FR

Funding

RECONSTITUTION OF HEDGEHOG SIGNALING COMPLEXR01CA082628 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ROBBINS, DAVID J · 1999 to 2014
$4.1M
Cancer Biology and Molecular TherapeuticsT32CA009658 · NCI · DARTMOUTH COLLEGE · PI EASTMAN, ALAN R · 1991 to 2011
$3.8M
NCI NIH HHS CA09658NCI NIH HHS CA8628NCI NIH HHS R01 CA082628NCI NIH HHS T32 CA009658
6 · The paper itself

Abstract

The Hedgehog (Hh) signaling pathway initiates an evolutionarily conserved developmental program required for the proper patterning of many tissues [1]. Although Costal2 (Cos2) is a requisite component of the Hh pathway, its mechanistic role is not well understood. Because of its primary sequence, Cos2 was initially predicted to function as a kinesin-like protein [2]. However, evidence showing that Cos2 function might require kinesin-like properties has been lacking [2-6]. Thus, the prevailing dogma in the field is that Cos2 functions solely as a scaffolding protein [7, 8]. Here, we show that Cos2 motility is required for its biological function and that this motility may be Hh regulated. We show that Cos2 motility requires an active motor domain, ATP, and microtubules. Additionally, Cos2 recruits and transports other components of the Hh signaling pathway, including the transcription factor Cubitus interruptus (Ci). Drosophila expressing cos2 mutations that encode proteins that lack motility are attenuated in their ability to regulate Ci activity and exhibit phenotypes consistent with attenuated Cos2 function [9]. Combined, these results demonstrate that Cos2 motility plays an important role in its function, regulating the amounts and activity of Ci that ultimately interpret the level of Hh to which cells are exposed.

Indexed as

Signal TransductionAnimalsCell LineDNA-Binding ProteinsDrosophilaDrosophila ProteinsHedgehog ProteinsKinesinsMolecular Motor ProteinsTranscription Factorsci protein, Drosophilacos protein, DrosophilaDNA-Binding ProteinsDrosophila ProteinsHedgehog Proteinshh protein, DrosophilaKinesinsMolecular Motor ProteinsTranscription Factors

Identifiers

PMID18691888
PMCPMC2774813
OpenAlexW2045399844

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.