Evidence map›Paper›PMID 33060357›Full record

ArticleScience (New York, N.Y.)2020

Engineering synthetic morphogen systems that can program multicellular patterning.

Satoshi Toda, Wesley L McKeithan, Teemu J Hakkinen, Pilar Lopez, Ophir D Klein, Wendell A Lim

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
–field-weighted citation impact
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

78 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Dynamical systems of fate and form in development.Seminars in cell & developmental biology · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Post-Transcriptional Modular Synthetic Receptors.bioRxiv : the preprint server for biology · 2024
    Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Satoshi TodaCell Design Institute, Department of Cellular and Molecular Pharmacology, and Howard Hughes Medical Institute, University of California San Francisco, San Francisco, CA 94158, USA. wendell.lim@ucsf.edu satoshi.toda@staff.kanazawa-u.ac.jp.ORCID 0000-0003-4997-9558
Wesley L McKeithanCell Design Institute, Department of Cellular and Molecular Pharmacology, and Howard Hughes Medical Institute, University of California San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0003-4413-6068
Teemu J HakkinenProgram in Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-3115-995X
Pilar LopezCell Design Institute, Department of Cellular and Molecular Pharmacology, and Howard Hughes Medical Institute, University of California San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0003-3219-6944
Ophir D KleinProgram in Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-6254-7082
Wendell A LimCell Design Institute, Department of Cellular and Molecular Pharmacology, and Howard Hughes Medical Institute, University of California San Francisco, San Francisco, CA 94158, USA. wendell.lim@ucsf.edu satoshi.toda@staff.kanazawa-u.ac.jp.ORCID 0000-0003-4052-8056

Funding

Harnessing natural stem cell-based strategies for mammalian dental renewalR35DE026602 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KLEIN, OPHIR D · 2016 to 2023
$8.0M
Cellular and molecular control of tooth morphogenesisR01DE028496 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GREEN, JEREMY B.A., KLEIN, OPHIR D · 2019 to 2023
$2.1M
Rebuilding a Micro-Organ: Using Synthetic Morphological Tools to Probe and Engineer the Structure and Function of Pancreatic IsletsF32DK123939 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCKEITHAN, WESLEY LAWRENCE · 2020 to 2020
$44k
Howard Hughes Medical InstituteNIDCR NIH HHS R01 DE028496NIDCR NIH HHS R35 DE026602NIDDK NIH HHS F32 DK123939
6 · The paper itself

Abstract

In metazoan tissues, cells decide their fates by sensing positional information provided by specialized morphogen proteins. To explore what features are sufficient for positional encoding, we asked whether arbitrary molecules (e.g., green fluorescent protein or mCherry) could be converted into synthetic morphogens. Synthetic morphogens expressed from a localized source formed a gradient when trapped by surface-anchoring proteins, and they could be sensed by synthetic receptors. Despite their simplicity, these morphogen systems yielded patterns reminiscent of those observed in vivo. Gradients could be reshaped by altering anchor density or by providing a source of competing inhibitor. Gradient interpretation could be altered by adding feedback loops or morphogen cascades to receiver cell response circuits. Orthogonal cell-cell communication systems provide insight into morphogen evolution and a platform for engineering tissues.

Indexed as

Body PatterningAnimalsDrosophila melanogasterFibroblastsGreen Fluorescent ProteinsProtein EngineeringReceptors, NotchTissue Engineeringgreen fluorescent protein, Aequorea victoriaGreen Fluorescent ProteinsReceptors, Notch

Identifiers

PMID33060357
PMCPMC7986291

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.