Abstract

    Huntington disease (HD) is a neurodegenerative disorder caused by a CAG tri-nucleotide expansion in the Huntingtin (Htt) gene. The disease is characterized by motor and behavioral symptoms associated with major neuropathology of mainly the caudate nucleus and cerebral cortex. I will briefly introduce weighted co-expression network analysis (WGCNA) and describe its application to analysis of several large sets of RNA-seq data. Specifically, I will start with a brief review of a consensus analysis of 3 striatum data sets that identified

13 modules strongly changed in HD models vs. control mice, revealing expression changes in major functional groups of genes. A separate consensus analysis of striatum and cerebellum data identified modules with similar as well as distinct response to CAG length expansion in these two brain regions. In particular, we identify a module enriched in markers of striatal medium spiny neuron genes that is sharply downregulated in striatum and upregulated in cerebellum in samples with high CAG length, suggesting defects in maintenance of cell identity gene expression programs in HD. I will also describe applications of WGCNA to aging and circadian data and their connection to molecular changes in HD.