Evidence map›Paper›PMID 40192104›Full record

ArticleeLife2025

A single-cell atlas of spatial and temporal gene expression in the mouse cranial neural plate.

Eric R Brooks, Andrew R Moorman, Bhaswati Bhattacharya, Ian S Prudhomme, Max Land, Heather L Alcorn, Roshan Sharma, Dana Pe'er, Jennifer A Zallen

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Eric R BrooksDepartment of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, United States.ORCID https://orcid.org/0000-0003-3159-8626
Andrew R MoormanHoward Hughes Medical Institute and Computational and Systems Biology Program, Sloan Kettering Institute, New York, United States.
Bhaswati BhattacharyaHoward Hughes Medical Institute and Developmental Biology Program, Sloan Kettering Institute, New York, United States.
Ian S PrudhommeHoward Hughes Medical Institute and Developmental Biology Program, Sloan Kettering Institute, New York, United States.
Max LandHoward Hughes Medical Institute and Computational and Systems Biology Program, Sloan Kettering Institute, New York, United States.
Heather L AlcornHoward Hughes Medical Institute and Developmental Biology Program, Sloan Kettering Institute, New York, United States.
Roshan SharmaHoward Hughes Medical Institute and Computational and Systems Biology Program, Sloan Kettering Institute, New York, United States.
Dana Pe'erHoward Hughes Medical Institute and Computational and Systems Biology Program, Sloan Kettering Institute, New York, United States.
Jennifer A ZallenHoward Hughes Medical Institute and Developmental Biology Program, Sloan Kettering Institute, New York, United States.ORCID https://orcid.org/0000-0003-3975-1568

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Control of cell behavior during cranial neural tube closureF32NS098832 · NINDS · SLOAN-KETTERING INST CAN RESEARCH · PI BROOKS, ERIC R · 2016 to 2018
$178k
NCI NIH HHS P30 CA008748NINDS NIH HHS F32 NS098832NINDS NIH HHS NS098832
6 · The paper itself

Abstract

The formation of the mammalian brain requires regionalization and morphogenesis of the cranial neural plate, which transforms from an epithelial sheet into a closed tube that provides the structural foundation for neural patterning and circuit formation. Sonic hedgehog (SHH) signaling is important for cranial neural plate patterning and closure, but the transcriptional changes that give rise to the spatially regulated cell fates and behaviors that build the cranial neural tube have not been systematically analyzed. Here, we used single-cell RNA sequencing to generate an atlas of gene expression at six consecutive stages of cranial neural tube closure in the mouse embryo. Ordering transcriptional profiles relative to the major axes of gene expression predicted spatially regulated expression of 870 genes along the anterior-posterior and mediolateral axes of the cranial neural plate and reproduced known expression patterns with over 85% accuracy. Single-cell RNA sequencing of embryos with activated SHH signaling revealed distinct SHH-regulated transcriptional programs in the developing forebrain, midbrain, and hindbrain, suggesting a complex interplay between anterior-posterior and mediolateral patterning systems. These results define a spatiotemporally resolved map of gene expression during cranial neural tube closure and provide a resource for investigating the transcriptional events that drive early mammalian brain development.

Indexed as

Gene Expression Regulation, DevelopmentalNeural PlateSingle-Cell AnalysisAnimalsEmbryo, MammalianGene Expression ProfilingHedgehog ProteinsMiceNeural TubeSequence Analysis, RNASignal TransductionHedgehog ProteinsShh protein, mousebrain developmentdevelopmental biologymousemouse embryoneural plateneural tube closurepatterningsingle-cell RNA sequencing

Identifiers

PMID40192104
PMCPMC11975377

What Socratic 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 Socratic graph.