Evidence map›Paper›PMID 32231307›Full record

ArticleNature cell biology2020

Single-cell chromatin accessibility maps reveal regulatory programs driving early mouse organogenesis.

Blanca Pijuan-Sala, Nicola K Wilson, Jun Xia, Xiaomeng Hou, Rebecca L Hannah, Sarah Kinston, Fernando J Calero-Nieto, Olivier Poirion, Sebastian Preissl, Feng Liu and 1 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 81 citations in OpenAlex.

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  13. Induction andbioRxiv : the preprint server for biology · 2024
    Article
  14. Transcription factors regulating vasculogenesis and angiogenesis.Developmental dynamics : an official publication of the American Association of Anatomists · 2024
    Review
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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

11 authors at 3 institutions in 3 countries.

Blanca Pijuan-SalaDepartment of Haematology, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-0922-9111
Nicola K WilsonDepartment of Haematology, University of Cambridge, Cambridge, UK.
Jun XiaState Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Xiaomeng HouCenter for Epigenomics, Department of Cellular and Molecular Medicine, University of California, San Diego, School of Medicine, La Jolla, CA, USA.
Rebecca L HannahDepartment of Haematology, University of Cambridge, Cambridge, UK.
Sarah KinstonDepartment of Haematology, University of Cambridge, Cambridge, UK.
Fernando J Calero-NietoDepartment of Haematology, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-3358-8253
Olivier PoirionCenter for Epigenomics, Department of Cellular and Molecular Medicine, University of California, San Diego, School of Medicine, La Jolla, CA, USA.
Sebastian PreisslCenter for Epigenomics, Department of Cellular and Molecular Medicine, University of California, San Diego, School of Medicine, La Jolla, CA, USA.ORCID http://orcid.org/0000-0001-8971-5616
Feng LiuState Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.ORCID http://orcid.org/0000-0003-3228-0943
Berthold GöttgensDepartment of Haematology, University of Cambridge, Cambridge, UK. bg200@cam.ac.uk.ORCID http://orcid.org/0000-0001-6302-5705
Wellcome/MRC Cambridge Stem Cell Institute · GBUniversity of California San Diego · USChinese Academy of Sciences · CN

Funding

Cancer Research UK 21762Medical Research Council MC_PC_12009Medical Research Council MR/S036113/1Wellcome Trust 105031Wellcome Trust 105031/Z/14/Z
6 · The paper itself

Abstract

During mouse embryonic development, pluripotent cells rapidly divide and diversify, yet the regulatory programs that define the cell repertoire for each organ remain ill-defined. To delineate comprehensive chromatin landscapes during early organogenesis, we mapped chromatin accessibility in 19,453 single nuclei from mouse embryos at 8.25 days post-fertilization. Identification of cell-type-specific regions of open chromatin pinpointed two TAL1-bound endothelial enhancers, which we validated using transgenic mouse assays. Integrated gene expression and transcription factor motif enrichment analyses highlighted cell-type-specific transcriptional regulators. Subsequent in vivo experiments in zebrafish revealed a role for the ETS factor FEV in endothelial identity downstream of ETV2 (Etsrp in zebrafish). Concerted in vivo validation experiments in mouse and zebrafish thus illustrate how single-cell open chromatin maps, representative of a mammalian embryo, provide access to the regulatory blueprint for mammalian organogenesis.

Indexed as

Enhancer Elements, GeneticGene Expression Regulation, DevelopmentalAnimalsCell LineageCell NucleusChromatinEmbryo, MammalianEmbryonic DevelopmentEmbryo, NonmammalianEndothelial CellsGene Expression ProfilingMiceMice, TransgenicOrganogenesisOrgan SpecificityProtein BindingChromatinER71 protein, mouseEtv2 protein, zebrafishFev protein, mouseTal1 protein, mouseT-Cell Acute Lymphocytic Leukemia Protein 1Transcription FactorsZebrafish Proteins

Identifiers

PMID32231307
PMCPMC7145456
OpenAlexW3012969293

What OpenQuestion holds

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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.