Evidence map›Paper›PMID 35363520›Full record

ArticleScience advances2022

Integrated single-cell transcriptomic and epigenetic study of cell state transition and lineage commitment in embryonic mouse cerebellum.

Nagham Khouri-Farah, Qiuxia Guo, Kerry Morgan, Jihye Shin, James Y H Li

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

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  20. Cerebellar development after preterm birth.Frontiers in cell and developmental biology · 2022
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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

5 authors at 1 institution in 1 country.

Nagham Khouri-FarahDepartment of Genetics and Genome Sciences, University of Connecticut School of Medicine, 263 Farmington Avenue, Farmington, CT 06030-6403, USA.ORCID 0000-0002-9849-8905
Qiuxia GuoDepartment of Genetics and Genome Sciences, University of Connecticut School of Medicine, 263 Farmington Avenue, Farmington, CT 06030-6403, USA.ORCID 0000-0002-6687-243X
Kerry MorganDepartment of Genetics and Genome Sciences, University of Connecticut School of Medicine, 263 Farmington Avenue, Farmington, CT 06030-6403, USA.
Jihye ShinDepartment of Genetics and Genome Sciences, University of Connecticut School of Medicine, 263 Farmington Avenue, Farmington, CT 06030-6403, USA.
James Y H LiDepartment of Genetics and Genome Sciences, University of Connecticut School of Medicine, 263 Farmington Avenue, Farmington, CT 06030-6403, USA.ORCID 0000-0002-9231-2698
University of Connecticut · US

Funding

Combinatorial function of Foxp1/2/4 in Purkinje cell diversification and cerebellar developmentR01NS120556 · NINDS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LI, JAMES Y.H · 2021 to 2025
$2.6M
MOLECULAR REGULATION OF LINEAGE SPECIFICATION OF THE MOUSE CEREBELLUMR01NS106844 · NINDS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LI, JAMES Y.H · 2018 to 2022
$2.1M
Studying the Molecular Mechanism of Foxp1/2 Function Controlling the Cerebellar DevelopmentF31NS124264 · NINDS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI FARAH, NAGHAM · 2021 to 2023
$128k
NINDS NIH HHS F31 NS124264NINDS NIH HHS R01 NS106844NINDS NIH HHS R01 NS120556
6 · The paper itself

Abstract

Recent studies using single-cell RNA-sequencing have revealed cellular heterogeneity in the developing mammalian cerebellum, yet the regulatory logic underlying this cellular diversity remains to be elucidated. Using integrated single-cell RNA and ATAC analyses, we resolved developmental trajectories of cerebellar progenitors and identified putative trans- and cis-elements that control cell state transition. We reverse engineered gene regulatory networks (GRNs) of each cerebellar cell type. Through in silico simulations and in vivo experiments, we validated the efficacy of GRN analyses and uncovered the molecular control of a posterior transitory zone (PTZ), a distinct progenitor zone residing immediately anterior to the morphologically defined rhombic lip (RL). We showed that perturbing cell fate specification in the PTZ and RL causes posterior cerebellar vermis hypoplasia, the most common cerebellar birth defect in humans. Our study provides a foundation for comprehensive studies of developmental programs of the mammalian cerebellum.

Indexed as

Nervous System MalformationsTranscriptomeAnimalsCell DifferentiationCerebellumEpigenesis, GeneticMammalsMice

Identifiers

PMID35363520
PMCPMC10938588
OpenAlexW4220957431

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.