These clustered Pcdh genes are found exclusively in vertebrates and are predominantly expressed in the nervous system. Distinct subsets of Pcdh genes are differentially expressed in individual neurons, and enormous cell surface diversity may result from combinatorial expression ( Esumi et al., 2005; Kaneko et al., 2006; Kohmura et al., 1998; Wang et al., 2002a). A subset of Pcdhg isoforms have been shown to engage in intercellular interactions that are strictly homophilic ( Schreiner and Weiner, 2010). The molecular diversity as well as the binding

specificity of clustered Pcdhs has led to the proposal that they provide a synaptic address code for neuronal connectivity or a single-cell barcode for self-recognition and self-avoidance similar to that ascribed to Dscam1 Lumacaftor concentration proteins of invertebrates ( Junghans et al., 2005; Serafini, 1999; Shapiro and Colman, 1999; Zipursky and Sanes, 2010). Genetic manipulations of individual

Pcdh gene clusters in mice have provided functional evidence that the clustered Pcdhs are required for normal development of the nervous system. Mutations in the Pcdha gene cluster have been reported to result in defects in olfactory sensory neuron axon coalescence and serotonergic axonal arborization as well as behavioral perturbations ( Fukuda et al., 2008; Hasegawa et al., 2008; VX-770 mw Katori et al., 2009). By contrast, abolishing Pcdhg function leads to neuronal apoptosis and synaptic loss in the spinal cord and retina (

Lefebvre et al., 2008; Prasad et al., 2008; Wang et al., 2002b; Weiner et al., 2005). Although these genetic studies have provided interesting insights into the roles of clustered Pcdhs in the nervous system, the functional significance of the diverse isoforms encoded by the three gene clusters is not understood. For example, it is unclear whether individual Pcdh isoforms within each cluster are functionally equivalent or whether certain isoforms may play distinct roles. The unique and highly conserved genomic organization of Pcdh gene clusters suggests that the isoform diversity Ridaforolimus (Deforolimus, MK-8669) and evolutionary diversification of Pcdh genes are central to understanding their function. In mice, the three Pcdh gene clusters each contain 14-22 homologous “variable” exons arrayed in tandem. Each variable exon is transcribed from its own promoter, and encodes the entire extracellular domain, a transmembrane domain, and a short intracellular domain of the corresponding Pcdh protein. In Pcdha and Pcdhg clusters (but not Pcdhb cluster), these variable exons are followed by a set of three “constant” exons, which are joined to each variable exon via cis-splicing to encode a common distal intracellular domain ( Tasic et al., 2002; Wang et al., 2002a).