Evidence map›Paper›PMID 33932341›Full record

ArticleCell2021

A single-embryo, single-cell time-resolved model for mouse gastrulation.

Markus Mittnenzweig, Yoav Mayshar, Saifeng Cheng, Raz Ben-Yair, Ron Hadas, Yoach Rais, Elad Chomsky, Netta Reines, Anna Uzonyi, Lior Lumerman and 5 more

Abstract read
In one paragraph

Article in Cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing 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

115 citing papers in PubMed.

  1. Article
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  5. bioRxiv : the preprint server for biology · 2026
    Article
  6. Science advances · 2026
    Article
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55 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Markus MittnenzweigDepartment of Computer Science and Applied Mathematics and Department of Biological Regulation, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Yoav MaysharDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Saifeng ChengDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Raz Ben-YairDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Ron HadasDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Yoach RaisDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Elad ChomskyDepartment of Computer Science and Applied Mathematics and Department of Biological Regulation, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Netta ReinesDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Anna UzonyiDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel; Department of Molecular Genetics, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Lior LumermanDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Aviezer LifshitzDepartment of Computer Science and Applied Mathematics and Department of Biological Regulation, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Zohar MukamelDepartment of Computer Science and Applied Mathematics and Department of Biological Regulation, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Ayelet-Hashahar OrenbuchDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Amos TanayDepartment of Computer Science and Applied Mathematics and Department of Biological Regulation, Weizmann Institute of Science, 7610001 Rehovot, Israel. Electronic address: amos.tanay@weizmann.ac.il.
Yonatan StelzerDepartment of Molecular Cell Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel. Electronic address: yonatan.stelzer@weizmann.ac.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mouse embryonic development is a canonical model system for studying mammalian cell fate acquisition. Recently, single-cell atlases comprehensively charted embryonic transcriptional landscapes, yet inference of the coordinated dynamics of cells over such atlases remains challenging. Here, we introduce a temporal model for mouse gastrulation, consisting of data from 153 individually sampled embryos spanning 36 h of molecular diversification. Using algorithms and precise timing, we infer differentiation flows and lineage specification dynamics over the embryonic transcriptional manifold. Rapid transcriptional bifurcations characterize the commitment of early specialized node and blood cells. However, for most lineages, we observe combinatorial multi-furcation dynamics rather than hierarchical transcriptional transitions. In the mesoderm, dozens of transcription factors combinatorially regulate multifurcations, as we exemplify using time-matched chimeric embryos of Foxc1/Foxc2 mutants. Our study rejects the notion of differentiation being governed by a series of binary choices, providing an alternative quantitative model for cell fate acquisition.

Indexed as

AnimalsCell DifferentiationCell LineageEmbryo, MammalianEmbryonic DevelopmentFemaleGastrulationGene ExpressionMiceMice, Inbred C57BLMouse Embryonic Stem CellsPregnancySequence Analysis, RNASingle-Cell Analysiscell fate decisionschimera assaydevelopmental biologymouse gastrulationnetwork flow modelscRNA-seqtetraploid complementation assaytrajectory inference

Identifiers

PMID33932341
PMCPMC8162424

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Registered trials

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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.