Evidence map›Paper›PMID 20956311›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Divergent and nonuniform gene expression patterns in mouse brain.

John A Morris, Joshua J Royall, Darren Bertagnolli, Andrew F Boe, Josh J Burnell, Emi J Byrnes, Cathy Copeland, Tsega Desta, Shanna R Fischer, Jeff Goldy and 19 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Unsupervised pattern identification in spatial gene expression atlas reveals mouse brain regions beyond established ontology.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Anatomical Diversity of the Adult Corticospinal Tract Revealed by Single-Cell Transcriptional Profiling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  4. Merged magnetic resonance and light sheet microscopy of the whole mouse brain.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Fibrinogen Chains Intrinsic to the Brain.Frontiers in neuroscience · 2019
    Article
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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

29 authors at 3 institutions in 1 country.

John A MorrisAllen Institute for Brain Science, Seattle, WA 98103, USA.
Joshua J Royall
Darren Bertagnolli
Andrew F Boe
Josh J Burnell
Emi J Byrnes
Cathy Copeland
Tsega Desta
Shanna R Fischer
Jeff Goldy
Katie J Glattfelder
Jolene M Kidney
Tracy Lemon
Geralyn J Orta
Sheana E Parry
Sayan D Pathak
Owen C Pearson
Melissa Reding
Sheila Shapouri
Kimberly A Smith
Chad Soden
Beth M Solan
John Weller
Joseph S Takahashi
Caroline C Overly
Ed S Lein
Michael J Hawrylycz
John G Hohmann
Allan R Jones
Allen Institute · USAllen Institute for Brain Science · USHoward Hughes Medical Institute · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Considerable progress has been made in understanding variations in gene sequence and expression level associated with phenotype, yet how genetic diversity translates into complex phenotypic differences remains poorly understood. Here, we examine the relationship between genetic background and spatial patterns of gene expression across seven strains of mice, providing the most extensive cellular-resolution comparative analysis of gene expression in the mammalian brain to date. Using comprehensive brainwide anatomic coverage (more than 200 brain regions), we applied in situ hybridization to analyze the spatial expression patterns of 49 genes encoding well-known pharmaceutical drug targets. Remarkably, over 50% of the genes examined showed interstrain expression variation. In addition, the variability was nonuniformly distributed across strain and neuroanatomic region, suggesting certain organizing principles. First, the degree of expression variance among strains mirrors genealogic relationships. Second, expression pattern differences were concentrated in higher-order brain regions such as the cortex and hippocampus. Divergence in gene expression patterns across the brain could contribute significantly to variations in behavior and responses to neuroactive drugs in laboratory mouse strains and may help to explain individual differences in human responsiveness to neuroactive drugs.

Indexed as

AnimalsBrainGene Expression ProfilingGene Expression RegulationHumansIn Situ HybridizationMiceSpecies Specificity

Identifiers

PMID20956311
PMCPMC2973884
OpenAlexW2020022521

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.