抄録
<jats:title>Abstract</jats:title><jats:p>Disruptions of the human <jats:italic>FOXP2</jats:italic> gene cause problems with articulation of complex speech sounds, accompanied by impairment in many aspects of language ability. The FOXP2/Foxp2 transcription factor is highly similar in humans and mice, and shows a complex conserved expression pattern, with high levels in neuronal subpopulations of the cortex, striatum, thalamus, and cerebellum. In the present study we generated mice in which <jats:italic>lox</jats:italic>P sites flank exons 12–14 of <jats:italic>Foxp2</jats:italic>; these exons encode the DNA‐binding motif, a key functional domain. We demonstrate that early global Cre‐mediated recombination yields a null allele, as shown by loss of the <jats:italic>lox</jats:italic>P‐flanked exons at the RNA level and an absence of Foxp2 protein. Homozygous null mice display severe motor impairment, cerebellar abnormalities and early postnatal lethality, consistent with other Foxp2 mutants. When crossed to transgenic lines expressing Cre protein in a spatially and/or temporally controlled manner, these conditional mice will provide new insights into the contributions of Foxp2 to distinct neural circuits, and allow dissection of roles during development and in the mature brain. genesis 45:440–446, 2007. Published 2007 Wiley‐Liss, Inc.</jats:p>
収録刊行物
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- genesis
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genesis 45 (7), 440-446, 2007-07
Wiley