Evidence map›Paper›PMID 24439388›Full record

ArticleCell2014

De novo inference of systems-level mechanistic models of development from live-imaging-based phenotype analysis.

Zhuo Du, Anthony Santella, Fei He, Michael Tiongson, Zhirong Bao

Abstract read
In one paragraph

Article in Cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed.

  1. Review
  2. Article
  3. Vacuolar HeLife · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Delineating the mechanisms and design principles ofComputational and structural biotechnology journal · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Lineage context switches the function of aDevelopment (Cambridge, England) · 2019
    Article
  19. A high-content imaging approach to profileDevelopment (Cambridge, England) · 2019
    Article
  20. Review
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

5 authors.

Zhuo DuDevelopmental Biology Program, Sloan-Kettering Institute, New York, NY 10065, USA.
Anthony SantellaDevelopmental Biology Program, Sloan-Kettering Institute, New York, NY 10065, USA.
Fei HeDevelopmental Biology Program, Sloan-Kettering Institute, New York, NY 10065, USA.
Michael TiongsonDevelopmental Biology Program, Sloan-Kettering Institute, New York, NY 10065, USA.
Zhirong BaoDevelopmental Biology Program, Sloan-Kettering Institute, New York, NY 10065, USA. Electronic address: baoz@mskcc.org.

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
The Ubiquitin-Proteasome System in Metazoan EmbryogenesisR01GM097576 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI BAO, ZHIRONG · 2011 to 2020
$3.3M
An integrated system to monitor complex tissues at single-cell resolutionU01HD075602 · NICHD · SLOAN-KETTERING INST CAN RESEARCH · PI BAO, ZHIRONG · 2012 to 2016
$3.1M
NICHD NIH HHS HD075602NICHD NIH HHS U01 HD075602NIGMS NIH HHS GM097576NIGMS NIH HHS R01 GM097576NIH HHS P40 OD010440
6 · The paper itself

Abstract

Elucidation of complex phenotypes for mechanistic insights presents a significant challenge in systems biology. We report a strategy to automatically infer mechanistic models of cell fate differentiation based on live-imaging data. We use cell lineage tracing and combinations of tissue-specific marker expression to assay progenitor cell fate and detect fate changes upon genetic perturbation. Based on the cellular phenotypes, we further construct a model for how fate differentiation progresses in progenitor cells and predict cell-specific gene modules and cell-to-cell signaling events that regulate the series of fate choices. We validate our approach in C. elegans embryogenesis by perturbing 20 genes in over 300 embryos. The result not only recapitulates current knowledge but also provides insights into gene function and regulated fate choice, including an unexpected self-renewal. Our study provides a powerful approach for automated and quantitative interpretation of complex in vivo information.

Indexed as

Cell LineageAnimalsCaenorhabditis elegansEmbryonic DevelopmentEmbryo, NonmammalianPhenotypeStem CellsTranscriptome

Identifiers

PMID24439388
PMCPMC3998820

What OpenQuestion holds

Textmetadata
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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.