Evidence map›Paper›PMID 20643350›Full record

ArticleDevelopmental cell2010

Role of lipid metabolism in smoothened derepression in hedgehog signaling.

Amir Yavari, Raghavendra Nagaraj, Edward Owusu-Ansah, Andrew Folick, Kathy Ngo, Tyler Hillman, Gerald Call, Rajat Rohatgi, Matthew P Scott, Utpal Banerjee

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Signaling in the primary cilium through the lens of the Hedgehog pathway.Wiley interdisciplinary reviews. Developmental biology · 2020
    Review
  10. Article
  11. Cellular homeostasis in theMolecular biology of the cell · 2020
    Article
  12. Article
  13. A Genetic Screen inG3 (Bethesda, Md.) · 2020
    Article
  14. Discovery of the Hedgehog Pathway Inhibitor Pipinib that Targets PI4KIIIß.Angewandte Chemie (International ed. in English) · 2019
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Amir YavariDepartment of Molecular, Cell, and Developmental Biology, Department of Biological Chemistry, Molecular Biology Institute, University of California Los Angeles, Los Angeles, CA 90095, USA.
Raghavendra Nagaraj
Edward Owusu-Ansah
Andrew Folick
Kathy Ngo
Tyler Hillman
Gerald Call
Rajat Rohatgi
Matthew P Scott
Utpal Banerjee
University of California, Los Angeles · USStanford University · USMidwestern University · US

Funding

Genomic and Genetic Dissection of Hematopoietic Development in DrosophilaR01HL067395 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SIEKHAUS, DARIA E · 2001 to 2025
$9.0M
Signaling and Metabolic Control in the Drosophila EyeR01EY008152 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BANERJEE, UTPAL · 1990 to 2015
$6.7M
Screening for drug targets in a Drosophila model of muscle degenerationF32AR057291 · NIAMS · HARVARD MEDICAL SCHOOL · PI OWUSU-ANSAH, EDWARD · 2009 to 2010
$101k
Howard Hughes Medical InstituteNEI NIH HHS R01 EY008152NEI NIH HHS R01EY008152NHLBI NIH HHS R01 HL067395NHLBI NIH HHS R01HL067395NIAMS NIH HHS F32 AR057291
6 · The paper itself

Abstract

The binding of Hedgehog (Hh) to its receptor Patched causes derepression of Smoothened (Smo), resulting in the activation of the Hh pathway. Here, we show that Smo activation is dependent on the levels of the phospholipid phosphatidylinositol-4 phosphate (PI4P). Loss of STT4 kinase, which is required for the generation of PI4P, exhibits hh loss-of-function phenotypes, whereas loss of Sac1 phosphatase, which is required for the degradation of PI4P, results in hh gain-of-function phenotypes in multiple settings during Drosophila development. Furthermore, loss of Ptc function, which results in the activation of Hh pathway, also causes an increase in PI4P levels. Sac1 functions downstream of STT4 and Ptc in the regulation of Smo membrane localization and Hh pathway activation. Taken together, our results suggest a model in which Ptc directly or indirectly functions to suppress the accumulation of PI4P. Binding of Hh to Ptc derepresses the levels of PI4P, which, in turn, promotes Smo activation.

Indexed as

Lipid Metabolism1-Phosphatidylinositol 4-KinaseAnimalsAnimals, Genetically ModifiedCaspase 3DrosophilaDrosophila ProteinsEyeGenes, InsectHedgehog ProteinsJNK Mitogen-Activated Protein KinasesMutationPhenotypePhosphatidylinositol PhosphatesPhosphoric Monoester HydrolasesReceptors, Cell Surface1-Phosphatidylinositol 4-KinaseCaspase 3dpp protein, DrosophilaDrosophila ProteinsHedgehog Proteinshh protein, DrosophilaJNK Mitogen-Activated Protein Kinasesphosphatidylinositol 4-phosphatePhosphatidylinositol PhosphatesPhosphoric Monoester Hydrolasesptc protein, DrosophilaReceptors, Cell SurfaceReceptors, G-Protein-CoupledSmoothened Receptorsmo protein, Drosophilawg protein, DrosophilaWnt1 Protein

Identifiers

PMID20643350
PMCPMC2945252
OpenAlexW2018340447

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.