Evidence map›Paper›PMID 28886385›Full record

ArticleCell2017

Combinatorial Signal Perception in the BMP Pathway.

Yaron E Antebi, James M Linton, Heidi Klumpe, Bogdan Bintu, Mengsha Gong, Christina Su, Reed McCardell, Michael B Elowitz

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 151 papers.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

151 citing papers in PubMed, 277 citations in OpenAlex.

  1. Article
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  5. Review
  6. Review
  7. Combinatorial decision-making driven by multicomponent surface condensates.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Trainable computation in molecular networks.bioRxiv : the preprint server for biology · 2025
    Article
  14. Article
  15. Article
  16. CryoEM structure of ALK2:BMP6 reveals distinct mechanism that allow ALK2 to interact with both BMP and activin ligands.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Review

91 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Yaron E AntebiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
James M LintonDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Heidi KlumpeDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Bogdan BintuDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Mengsha GongDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Christina SuDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Reed McCardellDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Michael B ElowitzDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; Howard Hughes Medical Institute and Department of Applied Physics, California Institute of Technology, Pasadena, CA 91125, USA. Electronic address: melowitz@caltech.edu.
California Institute of Technology · USHoward Hughes Medical Institute · US

Funding

UCLA-Caltech Medical Scientist Training ProgramT32GM008042 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AJIJOLA, OLUJIMI A, DAWSON, DAVID WAYNE · 1985 to 2023
$29.9M
Quantitative Single-Cell Analysis of Mammalian Notch Signaling StatesR01HD075335 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ELOWITZ, MICHAEL B · 2012 to 2024
$3.7M
NICHD NIH HHS R01 HD075335NIGMS NIH HHS T32 GM008042
6 · The paper itself

Abstract

The bone morphogenetic protein (BMP) signaling pathway comprises multiple ligands and receptors that interact promiscuously with one another and typically appear in combinations. This feature is often explained in terms of redundancy and regulatory flexibility, but it has remained unclear what signal-processing capabilities it provides. Here, we show that the BMP pathway processes multi-ligand inputs using a specific repertoire of computations, including ratiometric sensing, balance detection, and imbalance detection. These computations operate on the relative levels of different ligands and can arise directly from competitive receptor-ligand interactions. Furthermore, cells can select different computations to perform on the same ligand combination through expression of alternative sets of receptor variants. These results provide a direct signal-processing role for promiscuous receptor-ligand interactions and establish operational principles for quantitatively controlling cells with BMP ligands. Similar principles could apply to other promiscuous signaling pathways.

Indexed as

Signal TransductionAnimalsBone Morphogenetic ProteinsCell LineEmbryonic Stem CellsFeedbackFlow CytometryLigandsMiceModels, BiologicalNIH 3T3 CellsBone Morphogenetic ProteinsLigandsBMPbone morphogenetic proteinmultiplicitypromiscuity receptor-ligand interactionssignaling pathwayssignal perceptionsignal processingSMAD

Identifiers

PMID28886385
PMCPMC5612783
OpenAlexW2752405730

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.