g., creatine-targeting Ckb and 17-AAG-targeting buy DAPT Hsp90s) (Herbst and Wanker, 2007 and Dorsey and Shoulson, 2012). In summary, the red module contains proteins that are highly correlated with Htt (including Htt itself) and is enriched in a highly connected group of proteins involved in proteostasis,

14-3-3 signaling, microtubule-based transport, and mitochondria function. The second most Htt-correlated module is the blue module, with its member proteins enriched in the cortex and playing roles in presynaptic function. The most significant GO terms enriched in blue module are “Coated Membrane” and “Neurotransmitter Transport” (Table S14). The top IPA Canonical Signaling Pathways enriched in blue module are “GABA Receptor Signaling,” “Clathrin-Mediated Endocytosis,” and “Huntington’s Disease Signaling.” The hub proteins in blue module (Ap2a2, Dnm1, and Syt1) are members of a Htt protein network previously established based on ex vivo interactions with mHtt fragments and are validated as genetic modifiers in an HD fly model (Kaltenbach et al., 2007). Together, this evidence

supports the notion that the blue module contains cortex-enriched Htt interactors that preferentially function in presynaptic terminals and hence may influence corticostriatal neurotransmission that is known to be affected in HD (Raymond et al., 2011). The pink module is a cerebellum-enriched module with HD-relevant RAD001 manufacturer hub proteins functioning in calcium signaling (Itpr1 and Itpr2), mitochondria function (Ndufa9, Ndufs2, and Uqcrc2), and glutamate receptor function (Grid2 and Slc1a3). Not surprisingly,

several hub proteins are either selectively expressed (Grid2 and Slc1a3) or highly enriched in the cerebellum (Itpr1, Syt2, and Gpd1; see Allen Brain Atlas). Consistent with the idea that cerebellar-enriched Htt interactors may confer neuroprotective function, one interesting pink module protein, Ucqrc2, was shown to be one of nine core modulators of the proteostasis network (e.g., mHtt polyQ fragment and endogenous metastable proteins) in a genome-wide Caenorhabditis elegans screen ( Silva et al., 2011). Since our interactome also identified more Ucqrc2 peptides in brain tissues (cerebellum) and at ages (2 months) relatively unaffected Non-specific serine/threonine protein kinase in HD mice ( Table S7), this evidence strongly encourages further investigation in the role of Ucqrc2 and its interaction with Htt in HD selective pathogenesis. The yellow module is driven by top hub proteins involved in excitatory postsynaptic function (Table S14). Two of the top hub proteins (Grin2b/NR2b and Dlg4/PSD95) have been implicated in pathogenesis in HD mice (Zeron et al., 2002 and Fan et al., 2009). Another interesting member, beta-catenin (Ctnnb1), is a known modifier of mHtt-induced toxicity in HD cell and fly models (Godin et al., 2010 and Dupont et al., 2012).