Evidence map›Paper›PMID 35998232›Full record

ArticleScience signaling2022

PI(4,5)P

Jacob P Mahoney, Elise S Bruguera, Mansi Vasishtha, Lauren B Killingsworth, Saw Kyaw, William I Weis

Open access · greenAbstract read
In one paragraph

Article in Science signaling, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Jacob P MahoneyDepartments of Structural Biology and Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94035, USA.ORCID 0000-0002-7174-9161
Elise S BrugueraDepartments of Structural Biology and Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94035, USA.ORCID 0000-0003-1983-3013
Mansi VasishthaDepartments of Structural Biology and Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94035, USA.
Lauren B KillingsworthDepartments of Structural Biology and Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94035, USA.
Saw KyawDepartments of Structural Biology and Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94035, USA.
William I WeisDepartments of Structural Biology and Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94035, USA.ORCID 0000-0002-5583-6150
Stanford University · US

Funding

Stanford Center for Clinical & Translational Education and Research (Spectrum)UL1TR003142 · NCATS · STANFORD UNIVERSITY · PI O'HARA, RUTH M · 2019 to 2023
$45.0M
Molecular mechanisms of Wnt and mechanical signaling through β-cateninR35GM131747 · NIGMS · STANFORD UNIVERSITY · PI POKUTTA, SABINE · 2019 to 2023
$3.1M
Biochemical reconstitution of Wnt signaling complexesF32GM126642 · NIGMS · STANFORD UNIVERSITY · PI MAHONEY, JACOB P · 2017 to 2020
$186k
Molecular mechanism of Norrin signaling through Frizzled4 and LRP5/6F31EY031947 · NEI · STANFORD UNIVERSITY · PI BRUGUERA, ELISE · 2020 to 2022
$118k
NCATS NIH HHS UL1 TR003142NEI NIH HHS F31 EY031947NIGMS NIH HHS F32 GM126642NIGMS NIH HHS R35 GM131747
6 · The paper itself

Abstract

In the Wnt-β-catenin pathway, Wnt binding to Frizzled (Fzd) and LRP5 or LRP6 (LRP5/6) co-receptors inhibits the degradation of the transcriptional coactivator β-catenin by recruiting the cytosolic effector Dishevelled (Dvl). Polymerization of Dvl at the plasma membrane recruits the β-catenin destruction complex, enabling the phosphorylation of LRP5/6, a key step in inhibiting β-catenin degradation. Using purified Fzd proteins reconstituted in lipid nanodiscs, we investigated the factors that promote the recruitment of Dvl to the plasma membrane. We found that the affinity of Fzd for Dvl was not affected by Wnt ligands, in contrast to other members of the GPCR superfamily for which the binding of extracellular ligands affects the affinity for downstream transducers. Instead, Fzd-Dvl binding was enhanced by increased concentration of the lipid PI(4,5)P

Indexed as

beta CateninWnt Signaling PathwayDishevelled ProteinsFeedbackLipidsLow Density Lipoprotein Receptor-Related Protein-6PhosphoproteinsWnt Proteinsbeta CateninDishevelled ProteinsLipidsLow Density Lipoprotein Receptor-Related Protein-6PhosphoproteinsWnt Proteins

Identifiers

PMID35998232
PMCPMC9528458
OpenAlexW4292764296

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.