Evidence map›Paper›PMID 31712436›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Accelerated evolution of oligodendrocytes in the human brain.

Stefano Berto, Isabel Mendizabal, Noriyoshi Usui, Kazuya Toriumi, Paramita Chatterjee, Connor Douglas, Carol A Tamminga, Todd M Preuss, Soojin V Yi, Genevieve Konopka

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. 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
4.1field-weighted citation impact, top 5% 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
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  10. Primate gut microbiota induce evolutionarily salient changes in mouse neurodevelopment.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  11. Shaping the Neocortex: Radial Glia and Astrocytes in Development and Evolution.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  12. Article
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  15. Review
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  17. Rare Variant Analyses in Ancestrally Diverse Cohorts Reveal Novel ADHD Risk Genes.medRxiv : the preprint server for health sciences · 2025
    Article
  18. Article
  19. Review
  20. Accelerated cell-type-specific regulatory evolution of the human brain.Proceedings of the National Academy of Sciences of the United States of America · 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 4 institutions in 2 countries.

Stefano BertoDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Isabel MendizabalSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332.
Noriyoshi UsuiDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Kazuya ToriumiDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Paramita ChatterjeeSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332.
Connor DouglasDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Carol A TammingaDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Todd M PreussDivision of Neuropharmacology and Neurologic Diseases, Emory University, Atlanta, GA 30329.
Soojin V YiSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332; soojinyi@gatech.edu genevieve.konopka@utsouthwestern.edu.
Genevieve KonopkaDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390; soojinyi@gatech.edu genevieve.konopka@utsouthwestern.edu.ORCID 0000-0002-3363-7302
The University of Texas Southwestern Medical Center · USGeorgia Institute of Technology · USEmory University · USTokyo Metropolitan Matsuzawa Hospital · JP

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
REPRESSIVE HISTONE AND DNA METHYLATION IN RODENT DEPRESSION MODELSP50MH096890 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ALLIS, CHARLES DAVID · 2012 to 2021
$20.2M
Human Specific Brain DNA Methylation and Neuropsychiatric DiseasesR01MH103517 · NIMH · GEORGIA INSTITUTE OF TECHNOLOGY · PI JORDAN, IRVING KING, PREUSS, TODD M · 2015 to 2019
$3.5M
A National Chimpanzee Brain ResourceR24NS092988 · NINDS · GEORGE WASHINGTON UNIVERSITY · PI SHERWOOD, CHESTER · 2015 to 2018
$969k
NIH HHS P51 OD011132NIMH NIH HHS HHSN271201300030CNIMH NIH HHS P50 MH096890NIMH NIH HHS R01 MH103517NINDS NIH HHS R24 NS092988
6 · The paper itself

Abstract

Recent discussions of human brain evolution have largely focused on increased neuron numbers and changes in their connectivity and expression. However, it is increasingly appreciated that oligodendrocytes play important roles in cognitive function and disease. Whether both cell types follow similar or distinctive evolutionary trajectories is not known. We examined the transcriptomes of neurons and oligodendrocytes in the frontal cortex of humans, chimpanzees, and rhesus macaques. We identified human-specific trajectories of gene expression in neurons and oligodendrocytes and show that both cell types exhibit human-specific up-regulation. Moreover, oligodendrocytes have undergone more pronounced accelerated gene expression evolution in the human lineage compared to neurons. We highlighted human-specific coexpression networks with specific functions. Our data suggest that oligodendrocyte human-specific networks are enriched for alternative splicing and transcriptional regulation. Oligodendrocyte networks are also enriched for variants associated with schizophrenia and other neuropsychiatric disorders. Such enrichments were not found in neuronal networks. These results offer a glimpse into the molecular mechanisms of oligodendrocytes during evolution and how such mechanisms are associated with neuropsychiatric disorders.

Indexed as

Gene ExpressionAlternative SplicingAnimalsBiological EvolutionBrainCognitionGene Expression ProfilingGene Regulatory NetworksGenome-Wide Association StudyHumansMacaca mulattaMental DisordersOligodendrogliaPan troglodytesSpecies Specificitybrain evolutioncell-type expressioncomparative primate genomicsneurogenomics

Identifiers

PMID31712436
PMCPMC6883816
OpenAlexW2988542195

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.