bioRxiv · 10.1101/157016
Human-specific changes in two functional enhancers of FOXP2
Abstract
Two functional enhancers of FOXP2, a gene important for language development and evolution, exhibit several human-specific changes compared to extinct hominins that are located within the binding site for different transcription factors. Specifically, Neanderthals and Denisovans bear the ancestral allele in one position within the binding site for SMARCC1, involved in brain development and vitamin D metabolism. This change might have resulted in a different pattern of FOXP2 expression in our species compared to extinct hominins.
Explore related subjects
Keep this discovery
Benitez-Burraco, A., Torres-Ruiz, R., Gelabert Xirinachs, P., Lalueza-Fox, C., Rodriguez-Perales, S., Garcia-Bellido, P.. 2017-06-28. Human-specific changes in two functional enhancers of FOXP2. https://doi.org/10.1101/157016
Cite the original work for its findings. Save a collection to share your selection of sources.