Mapping of human FOXP2 enhancers reveals complex regulation

Martin Becker, Paolo Devanna, Simon E Fisher, Sonja C Vernes

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)


Mutations of the FOXP2 gene cause a severe speech and language disorder, providing a molecular window into the neurobiology of language. Individuals with FOXP2 mutations have structural and functional alterations affecting brain circuits that overlap with sites of FOXP2 expression, including regions of the cortex, striatum, and cerebellum. FOXP2 displays complex patterns of expression in the brain, as well as in non-neuronal tissues, suggesting that sophisticated regulatory mechanisms control its spatio-temporal expression. However, to date, little is known about the regulation of FOXP2 or the genomic elements that control its expression. Using chromatin conformation capture (3C), we mapped the human FOXP2 locus to identify putative enhancer regions that engage in long-range interactions with the promoter of this gene. We demonstrate the ability of the identified enhancer regions to drive gene expression. We also show regulation of the FOXP2 promoter and enhancer regions by candidate regulators - FOXP family and TBR1 transcription factors. These data point to regulatory elements that may contribute to the temporal- or tissue-specific expression patterns of human FOXP2. Understanding the upstream regulatory pathways controlling FOXP2 expression will bring new insight into the molecular networks contributing to human language and related disorders.

Original languageEnglish
Article number47
Number of pages15
JournalFrontiers in Molecular Neuroscience
Publication statusPublished - 21 Feb 2018


  • FOXP2
  • Enhancer elements
  • Genetic
  • Regulation of gene expression
  • Language
  • Language disorders
  • TBR1


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