Evidence map›Paper›PMID 35312478›Full record

ArticleeLife2022

Modular, robust, and extendible multicellular circuit design in yeast.

Alberto Carignano, Dai Hua Chen, Cannon Mallory, R Clay Wright, Georg Seelig, Eric Klavins

Abstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. A Modular and Customizable CRISPR/Cas Toolkit for Epigenome Editing of Cis-regulatory Modules.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  3. Review
  4. Article
  5. Article
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  7. 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

6 authors.

Alberto CarignanoDepartment of Electrical and Computer Engineering, University of Washington, Seattle, United States.ORCID 0000-0003-3306-9365
Dai Hua ChenDepartment of Electrical and Computer Engineering, University of Washington, Seattle, United States.
Cannon MalloryDepartment of Electrical and Computer Engineering, University of Washington, Seattle, United States.
R Clay WrightDepartment of Biological Systems Engineering, Virginia Tech, Blacksburg, United States.
Georg SeeligDepartment of Electrical and Computer Engineering, University of Washington, Seattle, United States.ORCID 0000-0002-3163-8782
Eric KlavinsDepartment of Electrical and Computer Engineering, University of Washington, Seattle, United States.ORCID 0000-0002-3805-5117

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Division of labor between cells is ubiquitous in biology but the use of multicellular consortia for engineering applications is only beginning to be explored. A significant advantage of multicellular circuits is their potential to be modular with respect to composition but this claim has not yet been extensively tested using experiments and quantitative modeling. Here, we construct a library of 24 yeast strains capable of sending, receiving or responding to three molecular signals, characterize them experimentally and build quantitative models of their input-output relationships. We then compose these strains into two- and three-strain cascades as well as a four-strain bistable switch and show that experimentally measured consortia dynamics can be predicted from the models of the constituent parts. To further explore the achievable range of behaviors, we perform a fully automated computational search over all two-, three-, and four-strain consortia to identify combinations that realize target behaviors including logic gates, band-pass filters, and time pulses. Strain combinations that are predicted to map onto a target behavior are further computationally optimized and then experimentally tested. Experiments closely track computational predictions. The high reliability of these model descriptions further strengthens the feasibility and highlights the potential for distributed computing in synthetic biology.

Indexed as

Saccharomyces cerevisiaeSynthetic BiologyGene LibraryLogicReproducibility of Resultsautomated circuit designcomputational biologyparallel computingS. cerevisiaesynthetic multicellular circuitsystems biology

Identifiers

PMID35312478
PMCPMC9000959

What OpenQuestion holds

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LicenceCC BY
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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.