Evidence map›Paper›PMID 22852769›Full record

ArticleBMC neuroscience2012

Hierarchical clustering of gene expression patterns in the Eomes + lineage of excitatory neurons during early neocortical development.

David A Cameron, Frank A Middleton, Anjen Chenn, Eric C Olson

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

David A CameronDepartment of Neuroscience and Physiology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Frank A Middleton
Anjen Chenn
Eric C Olson
SUNY Upstate Medical University · USNorthwestern University · US

Funding

Cellular and Molecular Mechanisms of Early Cortical DevelopmentR01NS066071 · NINDS · UPSTATE MEDICAL UNIVERSITY · PI OLSON, ERIC CHRISTOPHER · 2009 to 2013
$1.2M
NINDS NIH HHS NS066071NINDS NIH HHS R01 NS066071
6 · The paper itself

Abstract

backgroundCortical neurons display dynamic patterns of gene expression during the coincident processes of differentiation and migration through the developing cerebrum. To identify genes selectively expressed by the Eomes + (Tbr2) lineage of excitatory cortical neurons, GFP-expressing cells from Tg(Eomes::eGFP) Gsat embryos were isolated to > 99% purity and profiled.

resultsWe report the identification, validation and spatial grouping of genes selectively expressed within the Eomes + cortical excitatory neuron lineage during early cortical development. In these neurons 475 genes were expressed ≥ 3-fold, and 534 genes ≤ 3-fold, compared to the reference population of neuronal precursors. Of the up-regulated genes, 328 were represented at the Genepaint in situ hybridization database and 317 (97%) were validated as having spatial expression patterns consistent with the lineage of differentiating excitatory neurons. A novel approach for quantifying in situ hybridization patterns (QISP) across the cerebral wall was developed that allowed the hierarchical clustering of genes into putative co-regulated groups. Forty four candidate genes were identified that show spatial expression with Intermediate Precursor Cells, 49 candidate genes show spatial expression with Multipolar Neurons, while the remaining 224 genes achieved peak expression in the developing cortical plate.

conclusionsThis analysis of differentiating excitatory neurons revealed the expression patterns of 37 transcription factors, many chemotropic signaling molecules (including the Semaphorin, Netrin and Slit signaling pathways), and unexpected evidence for non-canonical neurotransmitter signaling and changes in mechanisms of glucose metabolism. Over half of the 317 identified genes are associated with neuronal disease making these findings a valuable resource for studies of neurological development and disease.

Indexed as

AnimalsCell DifferentiationCell LineageCerebral CortexCluster AnalysisDatabases, GeneticFlow CytometryGene Expression ProfilingGene Expression Regulation, DevelopmentalMiceMice, Inbred C57BLMice, TransgenicNerve Tissue ProteinsNeurogenesisNeuronsT-Box Domain ProteinsEomes protein, mouseNerve Tissue ProteinsT-Box Domain Proteins

Identifiers

PMID22852769
PMCPMC3583225
OpenAlexW2025579230

What OpenQuestion holds

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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.