Evidence map›Paper›PMID 36941249›Full record

ArticleNature communications2023

Single-cell transcriptomics uncovers a non-autonomous Tbx1-dependent genetic program controlling cardiac neural crest cell development.

Christopher De Bono, Yang Liu, Alexander Ferrena, Aneesa Valentine, Deyou Zheng, Bernice E Morrow

Open access · goldFull text read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. From a developmental atlas to maps of disease origin.Clinical and translational medicine · 2026
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  18. Heterogeneity of Wnt1-Cre-marked and Pax2-Cre-marked first branchial arch cranial neural crest cells in mice.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2024
    Article
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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

6 authors at 1 institution in 1 country.

Christopher De BonoDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA. christopher.debono@einsteinmed.edu.ORCID 0000-0002-4330-7155
Yang LiuDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0002-5804-0043
Alexander FerrenaDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0002-9578-8683
Aneesa ValentineDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
Deyou ZhengDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0003-4354-5337
Bernice E MorrowDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA. bernice.morrow@einsteinmed.edu.ORCID 0000-0002-8076-4726
Albert Einstein College of Medicine · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI STEVEN C. ALMO · 1985 to 2026
$111.2M
Project 2: Genetic Mechanisms of Non-syndromic Congenital Cardiac DefectsP01HD070454 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MORROW, BERNICE E · 2011 to 2020
$14.0M
SUPPORT FOR THE ROSE F KENNEDY IDDRC P50P50HD105352 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SOPHIE MOLHOLM, Steven Upshaw Walkley · 2021 to 2026
$7.0M
Cell fate choices by Tbx1 in forming the mammalian heartR01HL153920 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BERNICE E MORROW, Deyou Zheng · 2020 to 2026
$4.0M
The role of planar cell polarity signaling in outflow tract malformation in 22q11.2 deletion syndromeR01HL138470 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHANG, CHENBEI, WANG, JIANBO · 2017 to 2020
$2.6M
Molecular pathogenesis of congenital heart disease mediated by neural crest and second heart field cellsR01HL163667 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI MORROW, BERNICE E, ZHENG, DEYOU · 2022 to 2025
$2.5M
NCI NIH HHS P30 CA013330NHLBI NIH HHS R01 HL138470NHLBI NIH HHS R01 HL153920NHLBI NIH HHS R01 HL163667NICHD NIH HHS P01 HD070454NICHD NIH HHS P50 HD105352
6 · The paper itself

Abstract

Disruption of cardiac neural crest cells (CNCCs) results in congenital heart disease, yet we do not understand the cell fate dynamics as these cells differentiate to vascular smooth muscle cells. Here we performed single-cell RNA-sequencing of NCCs from the pharyngeal apparatus with the heart in control mouse embryos and when Tbx1, the gene for 22q11.2 deletion syndrome, is inactivated. We uncover three dynamic transitions of pharyngeal NCCs expressing Tbx2 and Tbx3 through differentiated CNCCs expressing cardiac transcription factors with smooth muscle genes. These transitions are altered non-autonomously by loss of Tbx1. Further, inactivation of Tbx2 and Tbx3 in early CNCCs results in aortic arch branching defects due to failed smooth muscle differentiation. Loss of Tbx1 interrupts mesoderm to CNCC cell-cell communication with upregulation and premature activation of BMP signaling and reduced MAPK signaling, as well as alteration of other signaling, and failed dynamic transitions of CNCCs leading to disruption of aortic arch artery formation and cardiac outflow tract septation.

Indexed as

Neural CrestTranscriptomeAnimalsAorta, ThoracicBranchial RegionCell DifferentiationMiceT-Box Domain ProteinsT-Box Domain ProteinsTbx1 protein, mouse

Identifiers

PMID36941249
PMCPMC10027855
OpenAlexW4328048326

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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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.