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Publication : Differential effects of Foxp2 disruption in distinct motor circuits.

First Author  French CA Year  2019
Journal  Mol Psychiatry Volume  24
Issue  3 Pages  447-462
PubMed ID  30108312 Mgi Jnum  J:315800
Mgi Id  MGI:6831330 Doi  10.1038/s41380-018-0199-x
Citation  French CA, et al. (2019) Differential effects of Foxp2 disruption in distinct motor circuits. Mol Psychiatry 24(3):447-462
abstractText  Disruptions of the FOXP2 gene cause a speech and language disorder involving difficulties in sequencing orofacial movements. FOXP2 is expressed in cortico-striatal and cortico-cerebellar circuits important for fine motor skills, and affected individuals show abnormalities in these brain regions. We selectively disrupted Foxp2 in the cerebellar Purkinje cells, striatum or cortex of mice and assessed the effects on skilled motor behaviour using an operant lever-pressing task. Foxp2 loss in each region impacted behaviour differently, with striatal and Purkinje cell disruptions affecting the variability and the speed of lever-press sequences, respectively. Mice lacking Foxp2 in Purkinje cells showed a prominent phenotype involving slowed lever pressing as well as deficits in skilled locomotion. In vivo recordings from Purkinje cells uncovered an increased simple spike firing rate and decreased modulation of firing during limb movements. This was caused by increased intrinsic excitability rather than changes in excitatory or inhibitory inputs. Our findings show that Foxp2 can modulate different aspects of motor behaviour in distinct brain regions, and uncover an unknown role for Foxp2 in the modulation of Purkinje cell activity that severely impacts skilled movements.
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