A humanized version of Foxp2 affects ultrasonic vocalization in adult female and male mice.
Sophie von MertenChristine PfeifleSven KünzelSvenja HoierDiethard TautzPublished in: Genes, brain, and behavior (2021)
The transcription factor FoxP2 is involved in setting up the neuronal circuitry for vocal learning in mammals and birds and is thought to have played a special role in the evolution of human speech and language. It has been shown that an allele with a humanized version of the murine Foxp2 gene changes the ultrasonic vocalization of mouse pups compared to pups of the wild-type inbred strain. Here we tested if this humanized allele would also affect the ultrasonic vocalization of adult female and male mice. In a previous study, in which only male vocalization was considered and the mice were recorded under a restricted spatial and temporal regime, no difference in adult vocalization between genotypes was found. Here, we use a different test paradigm in which both female and male vocalizations are recorded in extended social contact. We found differences in temporal, spectral and syntactical parameters between the genotypes in both sexes, and between sexes. Mice carrying the humanized Foxp2 allele were using higher frequencies and more complex syllable types than mice of the corresponding wildtype inbred strain. Our results support the notion that the humanized Foxp2 allele has a differential effect on mouse ultrasonic vocalization. As mice carrying the humanized version of the Foxp2 gene show effects opposite to those of mice carrying disrupted or mutated alleles of this gene, we conclude that this mouse line represents an important model for the study of human speech and language evolution.
Keyphrases
- regulatory t cells
- wild type
- high fat diet induced
- monoclonal antibody
- transcription factor
- endothelial cells
- copy number
- genome wide
- healthcare
- type diabetes
- insulin resistance
- magnetic resonance imaging
- psychometric properties
- optical coherence tomography
- young adults
- skeletal muscle
- functional connectivity
- subarachnoid hemorrhage
- resting state