Evidence map›Paper›PMID 34380046›Full record

ArticleCell2021

Whole-body integration of gene expression and single-cell morphology.

Hernando M Vergara, Constantin Pape, Kimberly I Meechan, Valentyna Zinchenko, Christel Genoud, Adrian A Wanner, Kevin Nzumbi Mutemi, Benjamin Titze, Rachel M Templin, Paola Y Bertucci and 10 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 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing 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

59 citing papers in PubMed.

  1. Review
  2. Article
  3. A pilot study for whole proteome tagging inbioRxiv : the preprint server for biology · 2026
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  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Segment Anything for Microscopy.Nature methods · 2025
    Article
  18. Single-cell Technology in Stem Cell Research.Current stem cell research & therapy · 2025
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Hernando M VergaraDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany; Sainsbury Wellcome Centre for Neural Circuits and Behaviour, Howland Street 25, London W1T 4JG, UK.
Constantin PapeCell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany; Heidelberg Collaboratory for Image Processing, Institut für Wissenschaftliches Rechnen, Ruprecht Karls Universität Heidelberg, Heidelberg, Germany.
Kimberly I MeechanCell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany; Collaboration for joint PhD degree between EMBL and Heidelberg University, Faculty of Biosciences.
Valentyna ZinchenkoCell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany; Collaboration for joint PhD degree between EMBL and Heidelberg University, Faculty of Biosciences.
Christel GenoudFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, Basel 4058, Switzerland; Electron Microscopy Facility, Faculty of Biology and Medicine, University of Lausanne, biophore, quartier Sorges, 1015 Lausanne, Switzerland.
Adrian A WannerFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, Basel 4058, Switzerland; Princeton Neuroscience Institute, Princeton University, Washington Road, Princeton, NJ 08544, USA; Paul Scherrer Institute (PSI), Forschungsstrasse 111, 5232 Villigen PSI, Switzerland.
Kevin Nzumbi MutemiDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany.
Benjamin TitzeFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, Basel 4058, Switzerland.
Rachel M TemplinCell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany.
Paola Y BertucciDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany.
Oleg SimakovDepartment of Neuroscience and Developmental Biology, University of Vienna, Althanstr. 14, Vienna 1090, Austria.
Wiebke DürichenDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany.
Pedro MachadoCentre for Ultrastructural Imaging, King's College London, New Hunt's House Guy's Campus, London SE1 1UL, UK.
Emily L SavageDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany.
Lothar SchermellehMicron Advanced Bioimaging Unit, Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Yannick SchwabCell Biology and Biophysics Unit/Electron Microscopy Core Facility, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany. Electronic address: yannick.schwab@embl.de.
Rainer W FriedrichFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, Basel 4058, Switzerland. Electronic address: rainer.friedrich@fmi.ch.
Anna KreshukCell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany. Electronic address: anna.kreshuk@embl.de.
Christian TischerCentre for Bioimage Analysis, Core Facilities, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany. Electronic address: christian.tischer@embl.de.
Detlev ArendtDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, Heidelberg 69117, Germany; Centre for Organismal Studies (COS), University of Heidelberg, Heidelberg, Germany. Electronic address: arendt@embl.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animal bodies are composed of cell types with unique expression programs that implement their distinct locations, shapes, structures, and functions. Based on these properties, cell types assemble into specific tissues and organs. To systematically explore the link between cell-type-specific gene expression and morphology, we registered an expression atlas to a whole-body electron microscopy volume of the nereid Platynereis dumerilii. Automated segmentation of cells and nuclei identifies major cell classes and establishes a link between gene activation, chromatin topography, and nuclear size. Clustering of segmented cells according to gene expression reveals spatially coherent tissues. In the brain, genetically defined groups of neurons match ganglionic nuclei with coherent projections. Besides interneurons, we uncover sensory-neurosecretory cells in the nereid mushroom bodies, which thus qualify as sensory organs. They furthermore resemble the vertebrate telencephalon by molecular anatomy. We provide an integrated browser as a Fiji plugin for remote exploration of all available multimodal datasets.

Indexed as

Cell ShapeGene Expression RegulationSingle-Cell AnalysisAnimalsCell NucleusGanglia, InvertebrateGene Expression ProfilingMultigene FamilyMultimodal ImagingMushroom BodiesPolychaetaautomatic segmentationcell typesgene expression atlasimage registrationmachine learningmultimodal data integrationmushroom bodiesPlatynereis dumeriliitelencephalonvolume electron microscopy

Identifiers

PMID34380046
PMCPMC8445025

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.