Evidence map›Paper›PMID 24550286›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

BMP signaling requires retromer-dependent recycling of the type I receptor.

Ryan J Gleason, Adenrele M Akintobi, Barth D Grant, Richard W Padgett

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.5field-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

54 citing papers in PubMed, 81 citations in OpenAlex.

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  18. Reciprocal interactions between transforming growth factor beta signaling and collagens: Insights from Caenorhabditis elegans.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Article
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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

4 authors at 1 institution in 2 countries.

Ryan J GleasonWaksman Institute of Microbiology, Department of Molecular Biology and Biochemistry, and Cancer Institute of New Jersey, Rutgers University, Piscataway, NJ 08854-8020.
Adenrele M Akintobi
Barth D Grant
Richard W Padgett
Czech Academy of Sciences, Institute of Microbiology · CZ

Funding

Membrane Traffic in C. elegans and MammalsR01GM067237 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI GRANT, BARTH DEMIAN · 2003 to 2019
$6.1M
Intercellular Signaling and Endosome to Golgi Transport in Multicellular AnimalsR01GM103995 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI GRANT, BARTH DEMIAN, PADGETT, RICHARD W. · 2013 to 2016
$1.2M
NIGMS NIH HHS R01 GM067237NIGMS NIH HHS R01 GM103995NIGMS NIH HHS R01GM103995NIGMS NIH HHS R01GM67237
6 · The paper itself

Abstract

The transforming growth factor β (TGFβ) superfamily of signaling pathways, including the bone morphogenetic protein (BMP) subfamily of ligands and receptors, controls a myriad of developmental processes across metazoan biology. Transport of the receptors from the plasma membrane to endosomes has been proposed to promote TGFβ signal transduction and shape BMP-signaling gradients throughout development. However, how postendocytic trafficking of BMP receptors contributes to the regulation of signal transduction has remained enigmatic. Here we report that the intracellular domain of Caenorhabditis elegans BMP type I receptor SMA-6 (small-6) binds to the retromer complex, and in retromer mutants, SMA-6 is degraded because of its missorting to lysosomes. Surprisingly, we find that the type II BMP receptor, DAF-4 (dauer formation-defective-4), is retromer-independent and recycles via a distinct pathway mediated by ARF-6 (ADP-ribosylation factor-6). Importantly, we find that loss of retromer blocks BMP signaling in multiple tissues. Taken together, our results indicate a mechanism that separates the type I and type II receptors during receptor recycling, potentially terminating signaling while preserving both receptors for further rounds of activation.

Indexed as

AnimalsAnimals, Genetically ModifiedBone Morphogenetic Protein Receptors, Type IBone Morphogenetic ProteinsCaenorhabditis elegansCaenorhabditis elegans ProteinsMicroscopy, FluorescenceMultiprotein ComplexesReal-Time Polymerase Chain ReactionReceptors, Cell SurfaceReceptors, Transforming Growth Factor betaRecombinant Fusion ProteinsSignal TransductionBone Morphogenetic Protein Receptors, Type IBone Morphogenetic ProteinsCaenorhabditis elegans Proteinsdaf-4 protein, C elegansMultiprotein ComplexesReceptors, Cell SurfaceReceptors, Transforming Growth Factor betaRecombinant Fusion ProteinsSMA-6 protein, C elegansC. elegansendocytosisreceptor trafficking

Identifiers

PMID24550286
PMCPMC3932876
OpenAlexW2034171109

What Socratic holds

Textmetadata
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 Socratic graph.