Evidence map›Paper›PMID 22876306›Full record

ArticlePloS one2012

Specialized motor-driven dusp1 expression in the song systems of multiple lineages of vocal learning birds.

Haruhito Horita, Masahiko Kobayashi, Wan-Chun Liu, Kotaro Oka, Erich D Jarvis, Kazuhiro Wada

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 52 citations in OpenAlex.

  1. Gene regulatory co-option drives birdsong neural circuit specialization.bioRxiv : the preprint server for biology · 2026
    Article
  2. Auditory Representation of Vocal Signals in a Pallial Cortical Circuit.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. HippocampalThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  8. Article
  9. Article
  10. Human Genomics and the Biocultural Origin of Music.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Brain evolution by brain pathway duplication.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  16. Article
  17. Article
  18. Audition-independent vocal crystallization associated with intrinsic developmental gene expression dynamics.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  19. Article
  20. 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

6 authors at 4 institutions in 2 countries.

Haruhito HoritaDepartment of Neurobiology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina, United States of America.
Masahiko Kobayashi
Wan-Chun Liu
Kotaro Oka
Erich D Jarvis
Kazuhiro Wada
Hokkaido University · JPHoward Hughes Medical Institute · USKeio University · JPRockefeller University · US

Funding

Sensory- and motor-driven genes in vocal communicationR01DC007218 · NIDCD · DUKE UNIVERSITY · PI JARVIS, ERICH D · 2005 to 2009
$1.6M
Howard Hughes Medical InstituteNIDCD NIH HHS R01 DC007218NIDCD NIH HHS R01DC7218NIH HHS DP1OD448
6 · The paper itself

Abstract

Mechanisms for the evolution of convergent behavioral traits are largely unknown. Vocal learning is one such trait that evolved multiple times and is necessary in humans for the acquisition of spoken language. Among birds, vocal learning is evolved in songbirds, parrots, and hummingbirds. Each time similar forebrain song nuclei specialized for vocal learning and production have evolved. This finding led to the hypothesis that the behavioral and neuroanatomical convergences for vocal learning could be associated with molecular convergence. We previously found that the neural activity-induced gene dual specificity phosphatase 1 (dusp1) was up-regulated in non-vocal circuits, specifically in sensory-input neurons of the thalamus and telencephalon; however, dusp1 was not up-regulated in higher order sensory neurons or motor circuits. Here we show that song motor nuclei are an exception to this pattern. The song nuclei of species from all known vocal learning avian lineages showed motor-driven up-regulation of dusp1 expression induced by singing. There was no detectable motor-driven dusp1 expression throughout the rest of the forebrain after non-vocal motor performance. This pattern contrasts with expression of the commonly studied activity-induced gene egr1, which shows motor-driven expression in song nuclei induced by singing, but also motor-driven expression in adjacent brain regions after non-vocal motor behaviors. In the vocal non-learning avian species, we found no detectable vocalizing-driven dusp1 expression in the forebrain. These findings suggest that independent evolutions of neural systems for vocal learning were accompanied by selection for specialized motor-driven expression of the dusp1 gene in those circuits. This specialized expression of dusp1 could potentially lead to differential regulation of dusp1-modulated molecular cascades in vocal learning circuits.

Indexed as

Gene ExpressionAnimalsBirdsBrainDual Specificity Phosphatase 1Early Growth Response Protein 1Gene Expression RegulationHigh Vocal CenterMaleMotor ActivityNeuronsSingingVerbal LearningDual Specificity Phosphatase 1Early Growth Response Protein 1

Identifiers

PMID22876306
PMCPMC3410896
OpenAlexW1989659369

What OpenQuestion holds

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Registered trials

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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.