Evidence map›Paper›PMID 40377146›Full record

ArticleDevelopment (Cambridge, England)2025

Small molecule- and cell contact-inducible systems for controlling expression and differentiation in mouse embryonic stem cells.

Sarah S Soliman, Devan H Shah, Hana El-Samad, Zara Y Weinberg

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

4 authors.

Sarah S SolimanDepartment of Biochemistry and Biophysics, University of California, San Francisco, CA 94158, USA.ORCID 0009-0003-8918-3332
Devan H ShahUC Berkeley-UCSF Graduate Program in Bioengineering, University of California, Berkeley, CA 94720-1762, USA.ORCID 0009-0003-1046-0713
Hana El-SamadDepartment of Biochemistry and Biophysics, University of California, San Francisco, CA 94158, USA.ORCID 0000-0001-6239-9916
Zara Y WeinbergDepartment of Biochemistry and Biophysics, University of California, San Francisco, CA 94158, USA.ORCID 0000-0001-7176-038X

Funding

UCSF IRACDA Scholars ProgramK12GM081266 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Raymond M. Esquerra, HOLLY A. INGRAHAM · 2007 to 2026
$19.4M
User-control and safetyU54CA244438 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIM, WENDELL A · 2019 to 2022
$7.8M
Synthetic circuits that drive infiltration of therapeutic T cells into immunologically cold tumorsU01CA265697 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EL-SAMAD, HANA, LIM, WENDELL A · 2021 to 2025
$2.9M
Understanding and rewiring cellular behavior with synthetic biology approachesK99GM147825 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WEINBERG, ZARA · 2023 to 2024
$250k
Chan-Zuckerberg InitiativeNCI NIH HHS U01 CA265697NCI NIH HHS U01CA265697NCI NIH HHS U54 CA244438NCI NIH HHS U54CA244438NIGMS NIH HHS 1K99GM147825NIGMS NIH HHS 5K12GM081266NIGMS NIH HHS K12 GM081266NIGMS NIH HHS K99 GM147825NIH HHS 1K99GM147825NIH HHS 5K12GM081266NIH HHS U54CA244438University of California
6 · The paper itself

Abstract

Synthetic developmental biology uses engineering approaches to understand multicellularity with goals ranging from recapitulating development to building synthetic organisms. Current approaches include engineering multicellular patterning, controlling differentiation and implementing cooperative cellular behaviors in model systems. Synthetic biology enables these pursuits by providing tools to control cell behavior. Mouse embryonic stem cells (mESCs) offer a well-studied and genetically tractable pluripotent model for pursuing synthetic development questions. However, there is minimal characterization of existing synthetic biology tools in mESCs. Here, we characterize three small molecule- and two cell contact-inducible systems for gene expression in and differentiation of mESCs. We show that small molecule- and cell contact-inducible systems work reliably and efficiently for controlling expression of arbitrary genetic payloads. We identify how these systems function differently across model differentiations. Furthermore, we show that these systems can drive direct differentiation of mESCs into neurons. Each of these systems can be used on their own or in combination, raising many possibilities for studying developmental principles with high precision.

Indexed as

Cell CommunicationCell DifferentiationGene Expression Regulation, DevelopmentalMouse Embryonic Stem CellsSmall Molecule LibrariesAnimalsMiceNeuronsSynthetic BiologySmall Molecule LibrariesCell engineeringDifferentiationGene expressionInducible systemsStem cellsSynthetic development

Identifiers

PMID40377146
PMCPMC12188245

What OpenQuestion holds

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LicenceCC BY
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.