Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Jan 6;375(1789):20190060.
doi: 10.1098/rstb.2019.0060. Epub 2019 Nov 18.

Birdsong as a window into language origins and evolutionary neuroscience

Affiliations
Review

Birdsong as a window into language origins and evolutionary neuroscience

Caitlin M Aamodt et al. Philos Trans R Soc Lond B Biol Sci. .

Erratum in

Abstract

Humans and songbirds share the key trait of vocal learning, manifested in speech and song, respectively. Striking analogies between these behaviours include that both are acquired during developmental critical periods when the brain's ability for vocal learning peaks. Both behaviours show similarities in the overall architecture of their underlying brain areas, characterized by cortico-striato-thalamic loops and direct projections from cortical neurons onto brainstem motor neurons that control the vocal organs. These neural analogies extend to the molecular level, with certain song control regions sharing convergent transcriptional profiles with speech-related regions in the human brain. This evolutionary convergence offers an unprecedented opportunity to decipher the shared neurogenetic underpinnings of vocal learning. A key strength of the songbird model is that it allows for the delineation of activity-dependent transcriptional changes in the brain that are driven by learned vocal behaviour. To capitalize on this advantage, we used previously published datasets from our laboratory that correlate gene co-expression networks to features of learned vocalization within and after critical period closure to probe the functional relevance of genes implicated in language. We interrogate specific genes and cellular processes through converging lines of evidence: human-specific evolutionary changes, intelligence-related phenotypes and relevance to vocal learning gene co-expression in songbirds. This article is part of the theme issue 'What can animal communication teach us about human language?'

Keywords: Bengalese finch; evolutionary neuroscience; neoteny; songbird; speech; zebra finch.

PubMed Disclaimer

Conflict of interest statement

We declare we have no competing interests.

Figures

Figure 1.
Figure 1.
Pie charts illustrate relationships between human intelligence eQTLs and songbird gene expression. (a) The expected distribution of overlap if there is no correlation between intelligence gene expression and genes underlying vocal variability in songbirds. (b) The observed correlation showing that, among directional gene expression changes correlated to intelligence, genes correlated to higher variability in songbirds are more likely to be downregulated in humans. (c) A control dataset showing a random distribution when using songbird genes with no correlation to vocal variability.

References

    1. Borges J. 1949. El Aleph. [In Spanish.] Buenos Aires, Argentina: Editorial Losada.
    1. Tyack PL. 2019. A taxonomy for vocal learning. Phil. Trans. R. Soc. B 375, 20180406 ( 10.1098/rstb.2018.0406) - DOI - PMC - PubMed
    1. Pfenning AR, et al. 2014. Convergent transcriptional specializations in the brains of humans and song-learning birds. Science 346, 1256846 ( 10.1126/science.1256846) - DOI - PMC - PubMed
    1. Ruhela RK, Prakash A, Medhi B. 2015. An urgent need for experimental animal model of autism in drug development. Ann. Neurosci. 22, 44–49. ( 10.5214/ans.0972.7531.220210) - DOI - PMC - PubMed
    1. Swerdlow NR, Light GA. 2016. Animal models of deficient sensorimotor gating in schizophrenia: are they still relevant? Curr. Top. Behav. Neurosci. 28, 305–325. ( 10.1007/7854_2015_5012) - DOI - PubMed

Publication types