Evidence map›Paper›PMID 19920144›Full record

ArticleThe Journal of biological chemistry2010

The full-length unprocessed hedgehog protein is an active signaling molecule.

Robert Tokhunts, Samer Singh, Tehyen Chu, Gisela D'Angelo, Valerie Baubet, John A Goetz, Zhen Huang, Ziqiang Yuan, Manuel Ascano, Yana Zavros and 4 more

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Bio-protocol · 2019
    Article
  7. The Journal of cell biology · 2019
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Hedgehog Signaling Links Chronic Inflammation to Gastric Cancer Precursor Lesions.Cellular and molecular gastroenterology and hepatology · 2017
    Review
  15. Review
  16. Hedgehog signaling in the stomach.Current opinion in pharmacology · 2016
    Review
  17. Review
  18. Article
  19. A new role for Hedgehogs in juxtacrine signaling.Mechanisms of development · 2014
    Article
  20. Review
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

14 authors.

Robert TokhuntsDepartment of Pharmacology and Toxicology, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.
Samer Singh
Tehyen Chu
Gisela D'Angelo
Valerie Baubet
John A Goetz
Zhen Huang
Ziqiang Yuan
Manuel Ascano
Yana Zavros
Pascal P Thérond
Sam Kunes
Nadia Dahmane
David J Robbins

Funding

Characterization of Sonic Hedgehog BiogenesisR01GM064011 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ROBBINS, DAVID J · 2002 to 2011
$2.6M
Characterization of Sonic Hedgehog BiogenesisR56GM064011 · NIGMS · DARTMOUTH COLLEGE · PI ROBBINS, DAVID J · 2007 to 2007
$327k
NIGMS NIH HHS GM64011NIGMS NIH HHS R01 GM064011NIGMS NIH HHS R56 GM064011
6 · The paper itself

Abstract

The hedgehog (HH) family of ligands plays an important instructional role in metazoan development. HH proteins are initially produced as approximately 45-kDa full-length proteins, which undergo an intramolecular cleavage to generate an amino-terminal product that subsequently becomes cholesterol-modified (HH-Np). It is well accepted that this cholesterol-modified amino-terminal cleavage product is responsible for all HH-dependent signaling events. Contrary to this model we show here that full-length forms of HH proteins are able to traffic to the plasma membrane and participate directly in cell-cell signaling, both in vitro and in vivo. We were also able to rescue a Drosophila eye-specific hh loss of function phenotype by expressing a full-length form of hh that cannot be processed into HH-Np. These results suggest that in some physiological contexts full-length HH proteins may participate directly in HH signaling and that this novel activity of full-length HH may be evolutionarily conserved.

Indexed as

Gene Expression Regulation, DevelopmentalHedgehog ProteinsAnimalsCell CommunicationChick EmbryoChickensDrosophilaDrosophila ProteinsEvolution, MolecularHoloprosencephalyHumansMutagenesis, Site-DirectedNeural TubePatched ReceptorsPhenotypeProtein Structure, TertiaryDrosophila ProteinsHedgehog Proteinshh protein, DrosophilaPatched ReceptorsReceptors, Cell SurfaceSHH protein, human

Identifiers

PMID19920144
PMCPMC2807313

What OpenQuestion holds

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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.