Evidence map›Paper›PMID 33290721›Full record

ArticleDevelopmental cell2020

Single-Cell Sequencing of Developing Human Gut Reveals Transcriptional Links to Childhood Crohn's Disease.

Rasa Elmentaite, Alexander D B Ross, Kenny Roberts, Kylie R James, Daniel Ortmann, Tomás Gomes, Komal Nayak, Liz Tuck, Sophie Pritchard, Omer Ali Bayraktar and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 185 papers.

0numbers the graph read from it
0cells of the map it votes in
185citing papers in PubMed
44.9field-weighted citation impact, top 1% of its field
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

185 citing papers in PubMed, 322 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. celltypeEnrich: a consensus-based scRNA-seq cluster annotation tool.bioRxiv : the preprint server for biology · 2026
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  13. RNA Helicase DDX21 Controls CD4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  15. Review
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125 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 1 country.

Rasa ElmentaiteWellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.
Alexander D B RossWellcome Trust, MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0SZ, UK; Department of Surgery, University of Cambridge, Cambridge CB2 0QQ, UK; Department of Paediatrics, University of Cambridge, Cambridge CB2 0QQ, UK.
Kenny RobertsWellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.
Kylie R JamesWellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.
Daniel OrtmannWellcome Trust, MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0SZ, UK; Department of Surgery, University of Cambridge, Cambridge CB2 0QQ, UK.
Tomás GomesWellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.
Komal NayakDepartment of Paediatrics, University of Cambridge, Cambridge CB2 0QQ, UK.
Liz TuckWellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.
Sophie PritchardWellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.
Omer Ali BayraktarWellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.
Robert HeuschkelDepartment of Paediatric Gastroenterology, Hepatology and Nutrition, Cambridge University Hospitals Trust, Cambridge CB2 0QQ, UK.
Ludovic VallierWellcome Trust, MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0SZ, UK; Department of Surgery, University of Cambridge, Cambridge CB2 0QQ, UK.
Sarah A TeichmannWellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK; Theory of Condensed Matter, Cavendish Laboratory, Department of Physics, University of Cambridge, Cambridge CB3 0HE, UK; European Molecular Biology Laboratory, European Bioinformatics Institute (EBI), Wellcome Genome Campus, Hinxton CB10 1SA, UK. Electronic address: st9@sanger.ac.uk.
Matthias ZilbauerWellcome Trust, MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0SZ, UK; Department of Paediatrics, University of Cambridge, Cambridge CB2 0QQ, UK; Department of Paediatric Gastroenterology, Hepatology and Nutrition, Cambridge University Hospitals Trust, Cambridge CB2 0QQ, UK. Electronic address: mz304@medschl.cam.ac.uk.
Wellcome Sanger Institute · GBCambridge University Hospitals NHS Foundation Trust · GBUniversity of Cambridge · GBWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

European Research Council 646794Medical Research Council G0701448Medical Research Council MC_PC_12009Medical Research Council MC_PC_17230Medical Research Council MR/T001917/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/N001540/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/T2T0419Wellcome Trust
6 · The paper itself

Abstract

Human gut development requires the orchestrated interaction of differentiating cell types. Here, we generate an in-depth single-cell map of the developing human intestine at 6-10 weeks post-conception. Our analysis reveals the transcriptional profile of cycling epithelial precursor cells; distinct from LGR5-expressing cells. We propose that these cells may contribute to differentiated cell subsets via the generation of LGR5-expressing stem cells and receive signals from surrounding mesenchymal cells. Furthermore, we draw parallels between the transcriptomes of ex vivo tissues and in vitro fetal organoids, revealing the maturation of organoid cultures in a dish. Lastly, we compare scRNA-seq profiles from pediatric Crohn's disease epithelium alongside matched healthy controls to reveal disease-associated changes in the epithelial composition. Contrasting these with the fetal profiles reveals the re-activation of fetal transcription factors in Crohn's disease. Our study provides a resource available at www.gutcellatlas.org, and underscores the importance of unraveling fetal development in understanding disease.

Indexed as

TranscriptomeAdolescentCells, CulturedChildCrohn DiseaseHumansIntestinal MucosaReceptors, G-Protein-CoupledRNA-SeqSingle-Cell AnalysisTranscription FactorsLGR5 protein, humanReceptors, G-Protein-CoupledTranscription Factorshuman fetal gut developmentinflammatory bowel diseaseintestinal organoidsintestinal stem cellspediatric Crohn's diseasesingle-cell RNA sequencingvillus formation

Identifiers

PMID33290721
PMCPMC7762816
OpenAlexW3110852430

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.