Evidence map›Paper›PMID 31831521›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2020

Genome-Wide Analysis of Differential Gene Expression and Splicing in Excitatory Neurons and Interneuron Subtypes.

Melanie A Huntley, Karpagam Srinivasan, Brad A Friedman, Tzu-Ming Wang, Ada X Yee, Yuanyuan Wang, Josh S Kaminker, Morgan Sheng, David V Hansen, Jesse E Hanson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

52 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. A neuron type-specific microexon inbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
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  12. Article
  13. Review
  14. Article
  15. Article
  16. H-Ras induces exuberantiScience · 2024
    Article
  17. Src dependency of the regulation of LTP by alternative splicing ofPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  18. Review
  19. Review
  20. Role of CAMK2D in neurodevelopment and associated conditions.American journal of human genetics · 2024
    Article
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

10 authors at 2 institutions in 2 countries.

Melanie A HuntleyDepartments of Bioinformatics and Computational Biology, and huntley.melanie@gene.com hanson.jesse@gene.com.
Karpagam SrinivasanNeuroscience, Genentech, Inc., South San Francisco, California 94080-4918.ORCID 0000-0001-8887-2767
Brad A FriedmanDepartments of Bioinformatics and Computational Biology, and.
Tzu-Ming WangNeuroscience, Genentech, Inc., South San Francisco, California 94080-4918.ORCID 0000-0002-6807-2129
Ada X YeeNeuroscience, Genentech, Inc., South San Francisco, California 94080-4918.
Yuanyuan WangNeuroscience, Genentech, Inc., South San Francisco, California 94080-4918.
Josh S KaminkerDepartments of Bioinformatics and Computational Biology, and.
Morgan ShengNeuroscience, Genentech, Inc., South San Francisco, California 94080-4918.
David V HansenNeuroscience, Genentech, Inc., South San Francisco, California 94080-4918.ORCID 0000-0001-9679-7189
Jesse E HansonNeuroscience, Genentech, Inc., South San Francisco, California 94080-4918 huntley.melanie@gene.com hanson.jesse@gene.com.
Posit Science (United States) · USGene Therapy Laboratory · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cortical circuit activity is shaped by the parvalbumin (PV) and somatostatin (SST) interneurons that inhibit principal excitatory (EXC) neurons and the vasoactive intestinal peptide (VIP) interneurons that suppress activation of other interneurons. To understand the molecular-genetic basis of functional specialization and identify potential drug targets specific to each neuron subtype, we performed a genome wide assessment of both gene expression and splicing across EXC, PV, SST and VIP neurons from male and female mouse brains. These results reveal numerous examples where neuron subtype-specific gene expression, as well as splice-isoform usage, can explain functional differences between neuron subtypes, including in presynaptic plasticity, postsynaptic receptor function, and synaptic connectivity specification. We provide a searchable web resource for exploring differential mRNA expression and splice form usage between excitatory, PV, SST, and VIP neurons (http://research-pub.gene.com/NeuronSubtypeTranscriptomes). This resource, combining a unique new dataset and novel application of analysis methods to multiple relevant datasets, identifies numerous potential drug targets for manipulating circuit function, reveals neuron subtype-specific roles for disease-linked genes, and is useful for understanding gene expression changes observed in human patient brains.

Indexed as

TranscriptomeAnimalsCells, CulturedCerebral CortexFemaleHippocampusInterneuronsMaleMice, TransgenicNeuronsParvalbuminsRNA, MessengerSomatostatinVasoactive Intestinal PeptideParvalbuminsRNA, MessengerSomatostatinVasoactive Intestinal PeptideinterneuronpsychiatricPVsplicingSSTVIP

Identifiers

PMID31831521
PMCPMC6988999
OpenAlexW2996707411

What OpenQuestion holds

Textmetadata
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.