Evidence map›Paper›PMID 18362152›Full record

ArticleThe Journal of biological chemistry2008

Wnt signal amplification via activity, cooperativity, and regulation of multiple intracellular PPPSP motifs in the Wnt co-receptor LRP6.

Bryan T MacDonald, Chika Yokota, Keiko Tamai, Xin Zeng, Xi He

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

59 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. LRPs in WNT Signalling.Handbook of experimental pharmacology · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis.Genetics in medicine : official journal of the American College of Medical Genetics · 2016
    Article
  18. Article
  19. Wnt pathway activation by ADP-ribosylation.Nature communications · 2016
    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 at 2 institutions in 1 country.

Bryan T MacDonaldF. M. Kirby Neurobiology Center, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115, USA.
Chika Yokota
Keiko Tamai
Xin Zeng
Xi He
Boston Children's Hospital · USHarvard University · US

Funding

Wnt/beta-catenin signaling: phosphorylation regulation of Wnt receptor-Axin interR01GM074241 · NIGMS · CHILDREN'S HOSPITAL BOSTON · PI HE, XI · 2005 to 2013
$2.5M
Wnt co-receptor phosphorylation and activationF32GM073357 · NIGMS · CHILDREN'S HOSPITAL BOSTON · PI MACDONALD, BRYAN THOMAS · 2005 to 2007
$137k
NIGMS NIH HHS F32 GM073357NIGMS NIH HHS R01 GM074241NIGMS NIH HHS R01 GM74241
6 · The paper itself

Abstract

Low density lipoprotein receptor-related protein 6 (LRP6) and its homologue LRP5 serve as Wnt co-receptors that are essential for the Wnt/beta-catenin pathway. Wnt activation of LRP6 leads to recruitment of the scaffolding protein Axin and inhibition of Axin-mediated phosphorylation/destruction of beta-catenin. We showed that five conserved PPPSP motifs in the LRP6 intracellular domain are required for LRP6 function, and mutation of these motifs together abolishes LRP6 signaling activity. We further showed that Wnt induces the phosphorylation of a prototypic PPPSP motif, which provides a docking site for Axin and is sufficient to transfer signaling activity to a heterologous receptor. However, the activity, regulation, and functionality of multiple PPPSP motifs in LRP6 have not been characterized. Here we provide a comprehensive analysis of all five PPPSP motifs in LRP6. We define the core amino acid residues of a prototypic PPPSP motif via alanine scanning mutagenesis and demonstrate that each of the five PPPSP motifs exhibits signaling and Axin binding activity in isolation. We generated two novel phosphorylation-specific antibodies to additional PPPSP motifs and show that Wnt induces phosphorylation of these motifs in the endogenous LRP6 through glycogen synthase kinase 3. Finally, we uncover the critical cooperativity of PPPSP motifs in the full-length LRP6 by demonstrating that LRP6 mutants lacking a single PPPSP motif display compromised function, whereas LRP6 mutants lacking two of the five PPPSP motifs are mostly inactive. This cooperativity appears to reflect the ability of PPPSP motifs to promote the phosphorylation of one another and to interact with Axin synergistically. These results establish the critical role and a common phosphorylation/activation mechanism for the PPPSP motifs in LRP6 and suggest that the conserved multiplicity and cooperativity of the PPPSP motifs represents a built-in amplifier for Wnt signaling by the LRP6 family of receptors.

Indexed as

AnimalsAxin ProteinHumansLDL-Receptor Related ProteinsLow Density Lipoprotein Receptor-Related Protein-5Low Density Lipoprotein Receptor-Related Protein-6MutagenesisPhosphorylationRepressor ProteinsSignal TransductionWnt ProteinsXenopus laevisXenopus Proteinsaxin1 protein, XenopusAxin ProteinLDL-Receptor Related ProteinsLow Density Lipoprotein Receptor-Related Protein-5Low Density Lipoprotein Receptor-Related Protein-6LRP5 protein, humanLRP6 protein, humanRepressor ProteinsWnt ProteinsXenopus Proteins

Identifiers

PMID18362152
PMCPMC2414294
OpenAlexW2007886374

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.