Evidence map›Paper›PMID 42032312›Full record

ArticleNature cell biology2026

The proteomic landscape and temporal dynamics of human and mouse gastruloid development.

Riddhiman K Garge, Valerie Lynch, Rose Fields, Silvia Casadei, Sabrina Best, Jeremy Stone, Matthew Snyder, Connor Kubo, Arata Wakimoto, Zukai Liu and 5 more

Abstract read
In one paragraph

Article in Nature cell biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Riddhiman K GargeDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. rgarge@uw.edu.ORCID http://orcid.org/0000-0002-6774-0172
Valerie LynchDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Rose FieldsDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Silvia CasadeiDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Sabrina BestBrotman Baty Institute for Precision Medicine, Seattle, WA, USA.
Jeremy StoneBrotman Baty Institute for Precision Medicine, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-7565-2463
Matthew SnyderBrotman Baty Institute for Precision Medicine, Seattle, WA, USA.ORCID http://orcid.org/0000-0001-7433-4343
Connor KuboDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0001-9579-2917
Arata WakimotoSeattle Hub for Synthetic Biology, Seattle, WA, USA.
Zukai LiuDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0001-5738-4357
Chris D McGannDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0001-9379-1910
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. shendure@uw.edu.ORCID http://orcid.org/0000-0002-1516-1865
Lea M StaritaDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. lstarita@uw.edu.ORCID http://orcid.org/0000-0003-2870-5099
Nobuhiko HamazakiDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. hamazaki@uw.edu.ORCID http://orcid.org/0000-0001-9228-233X
Devin K SchweppeDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. dkschwep@uw.edu.ORCID http://orcid.org/0000-0002-3241-6276

Funding

Technology for evaluating drug-binding responses to small-molecule perturbationR35GM150919 · NIGMS · UNIVERSITY OF WASHINGTON · PI Devin Karl Schweppe · 2023 to 2026
$1.6M
NIGMS NIH HHS R35 GM150919U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) 1RM1HG010461U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM150919
6 · The paper itself

Abstract

The embryo establishes a body plan and primes itself for organogenesis during gastrulation. As gastrulation is challenging to study in vivo, stem-cell-derived 'gastruloids' have emerged as powerful surrogates. Although transcriptomics and imaging have been applied extensively to such embryo models, the dynamics of their proteomes remains largely unknown. Here we apply quantitative proteomics to human and mouse gastruloids at four key stages. We leverage these data to map the expression dynamics of protein complexes, and to nominate cooperative proteins. With matched transcriptome data, we investigate global and stage-specific discordance between the transcriptome and proteome and leverage phosphosite dynamics to nominate kinase-substrate relationships. Finally, we apply co-regulation network analysis to identify genes linked to the Commander complex, the perturbation of which leads to morphological defects in gastruloids. Altogether, our work showcases the potential of applying proteomics to embryo models to advance our understanding of mammalian development in ways challenging through transcriptomics alone.

Indexed as

GastrulaGastrulationProteomeProteomicsAnimalsGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansMiceTranscriptomeProteome

Identifiers

PMID42032312
PMCPMC13179132

What OpenQuestion holds

Textmetadata
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.