Evidence map›Paper›PMID 26014473›Full record

ArticleDevelopmental neurobiology2016

Temporal patterns of gene expression during calyx of held development.

Douglas R Kolson, Jun Wan, Jonathan Wu, Marlin Dehoff, Ashley N Brandebura, Jiang Qian, Peter H Mathers, George A Spirou

Open access · greenAbstract read
In one paragraph

Article in Developmental neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 27 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

8 authors at 3 institutions in 1 country.

Douglas R KolsonSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, West Virginia.
Jun WanWilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Jonathan WuSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, West Virginia.
Marlin DehoffSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, West Virginia.
Ashley N BrandeburaSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, West Virginia.
Jiang QianWilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Peter H MathersSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, West Virginia.
George A SpirouSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, West Virginia.
West Virginia University · USJohns Hopkins Medicine · USJohns Hopkins University · US

Funding

Development of the Calyx of HeldR01DC007695 · NIDCD · WEST VIRGINIA UNIVERSITY · PI GEORGE A SPIROU, HENRIQUE Prado VON GERSDORFF · 2007 to 2026
$6.2M
COBRE Transitional Center in NeuroscienceP30GM103503 · NIGMS · WEST VIRGINIA UNIVERSITY · PI SPIROU, GEORGE A · 2012 to 2014
$3.2M
NIDCD NIH HHS DC007695NIDCD NIH HHS DC007695-S1NIDCD NIH HHS R01 DC007695NIGMS NIH HHS GM103105NIGMS NIH HHS P30 GM103503
6 · The paper itself

Abstract

Relating changes in gene expression to discrete developmental events remains an elusive challenge in neuroscience, in part because most neural territories are comprised of multiple cell types that mature over extended periods of time. The medial nucleus of the trapezoid body (MNTB) is an attractive vertebrate model system that contains a nearly homogeneous population of neurons, which are innervated by large glutamatergic nerve terminals called calyces of Held (CH). Key steps in maturation of CHs and MNTB neurons, including CH growth and competition, occur very quickly for most cells between postnatal days (P)2 and P6. Therefore, we characterized genome-wide changes in this system, with dense temporal sampling during the first postnatal week. We identified 541 genes whose expression changed significantly between P0-6 and clustered them into eight groups based on temporal expression profiles. Candidate genes from each of the eight profile groups were validated in separate samples by qPCR. Our tissue sample permitted comparison of known glial and neuronal transcripts and revealed that monotonically increasing or decreasing expression profiles tended to be associated with glia and neurons, respectively. Gene ontology revealed enrichment of genes involved in axon pathfinding, cell differentiation, cell adhesion and extracellular matrix. The latter category included elements of perineuronal nets, a prominent feature of MNTB neurons that is morphologically distinct by P6, when CH growth and competition are resolved onto nearly all MNTB neurons. These results provide a genetic framework for investigation of general mechanisms responsible for nerve terminal growth and maturation.

Indexed as

AnimalsAuditory PathwaysAxonsBrain StemExtracellular MatrixGene Expression Regulation, DevelopmentalMiceNeurogliaNeuronsSynapsescalyx of helddevelopmentmicroarrayMNTBperineuronal net

Identifiers

PMID26014473
PMCPMC4851834
OpenAlexW2131482889

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.