Control of Huntington's Disease-Associated Phenotypes by the Striatum-Enriched Transcription Factor Foxp2

• Autor(a) principal: Hachigian, Lea J.
• Data de Publicação: 2017
• Outros Autores: Carmona, Vitor, Fenster, Robert J., Kulicke, Ruth, Heilbut, Adrian, Sittler, Annie, Almeida, Luís Pereira de, Mesirov, Jill P., Gao, Fan, Kolaczyk, Eric D., Heiman, Myriam
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10316/108127; https://doi.org/10.1016/j.celrep.2017.11.018
• topic: Foxp2; Huntington’s disease; corticostriatal synapse; striatum; Animals; Blotting, Western; Corpus Striatum; Disease Models, Animal; Fluorescent Antibody Technique, Indirect; Forkhead Transcription Factors; Gene Expression Regulation; Humans; Huntington Disease; Male; Mice; Phenotype; Repressor Proteins

Alteration of corticostriatal glutamatergic function is an early pathophysiological change associated with Huntington's disease (HD). The factors that regulate the maintenance of corticostriatal glutamatergic synapses post-developmentally are not well understood. Recently, the striatum-enriched transcription factor Foxp2 was implicated in the development of these synapses. Here, we show that, in mice, overexpression of Foxp2 in the adult striatum of two models of HD leads to rescue of HD-associated behaviors, while knockdown of Foxp2 in wild-type mice leads to development of HD-associated behaviors. We note that Foxp2 encodes the longest polyglutamine repeat protein in the human reference genome, and we show that it can be sequestered into aggregates with polyglutamine-expanded mutant Huntingtin protein (mHTT). Foxp2 overexpression in HD model mice leads to altered expression of several genes associated with synaptic function, genes that present additional targets for normalization of corticostriatal dysfunction in HD.