Abstract

The generation of complex neural circuits depends on the correct wiring of neurons with diverse individual characteristics. To understand the complexity of the nervous system, the molecular mechanisms for specifying the identity and diversity of individual neurons must be elucidated. The clustered protocadherins (Pcdh) in mammals consist of approximately 50 Pcdh genes (Pcdh-α, Pcdh-β, and Pcdh-γ) that encode cadherin-family cell surface adhesion proteins. Individual neurons express a random combination of Pcdh-α and Pcdh-γ, whereas the expression patterns for the Pcdh-β genes, 22 one-exon genes in mouse, are not fully understood. Here we show that the Pcdh-β genes are expressed in a 3′-polyadenylated form in mouse brain. In situ hybridization using a pan-Pcdh-β probe against a conserved Pcdh-β sequence showed widespread labeling in the brain, with prominent signals in the olfactory bulb, hippocampus, and cerebellum. In situ hybridization with specific probes for individual Pcdh-β genes showed their expression to be scattered in Purkinje cells from P10 to P150. The scattered expression patterns were confirmed by performing a newly developed single-cell 3′-RACE analysis of Purkinje cells, which clearly demonstrated that the Pcdh-β genes are expressed monoallelically and combinatorially in individual Purkinje cells. Scattered expression patterns of individual Pcdh-β genes were also observed in pyramidal neurons in the hippocampus and cerebral cortex, neurons in the trigeminal and dorsal root ganglion, GABAergic interneurons, and cholinergic neurons. Our results extend previous observations of diversity at the single-neuron level generated by Pcdh expression and suggest that the Pcdh-β cluster genes contribute to specifying the identity and diversity of individual neurons.

Highlights

  • The central and peripheral nervous systems contain an enormous number of neurons, that have diverse characteristics and unique identities that enable them to generate complex neural circuits

  • Because the DNA sequence that corresponds to extracellular cadherin domain 4 (EC4)-EC5-EC6 of Pcdh-β12 is highly conserved from β2 to β22, we used this sequence as a pan-Pcdh-β probe (Pcdh-β highly conserved probe, hereafter) to detect all 21 isoforms of Pcdh-β

  • Our results revealed that the Pcdh-β isoforms showed randomlike scattered expression in both the central and the peripheral nervous systems, and that the Pcdh-β genes were regulated monoallelically and combinatorially in single Purkinje cells

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Summary

Introduction

The central and peripheral nervous systems contain an enormous number of neurons, that have diverse characteristics and unique identities that enable them to generate complex neural circuits. Elucidating the molecular mechanisms that specify the unique characteristics of individual neurons is important for understanding the overall complexity of the nervous system. Recent studies reported that two families of cell-cell recognition molecules, Dscam in insects and clustered protocadherin (Pcdh) in vertebrates, are promising candidates for specifying the unique characteristics of individual neurons (Zipursky and Sanes, 2010; Yagi, 2012). The fly Dscam gene encodes 19,008 different ectodomain isoforms, which are expressed in a biased stochastic fashion in individual neurons, thereby conferring a unique molecular identity on each Drosophila neuron (Neves et al, 2004). Hattori et al (2007) showed that Dscam diversity is essential for generating complex neural circuits

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