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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSM1230365 1"/></item><item><item key="GSM1230366 1"/></item><item><item key="GSM1230367 1"/></item><item><item key="GSM1230368 1"/></item><item><item key="GSM1230369 1"/></item><item><item key="GSM1230370 1"/></item><item><item key="GSM1230371 1"/></item><item><item key="GSM1230372 1"/></item><item><item key="GSM1230373 1"/></item><item><item key="GSM1230374 1"/></item><item><item key="GSM1230375 1"/></item><item><item key="GSM1230376 1"/></item></item><item key="id">7429</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">The &#946; subunits of voltage-gated calcium channels regulate surface expression and gating of CaV1 and CaV2 &#945;1 subunits, and thus contribute...</item><item key="geo_gse_id">E-GEOD-50822</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">12</item><item key="tags"><item>axon</item><item>cerebellum</item><item>distal</item><item>genome</item><item>surface</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">differential-neuronal-targeting-of-a-new-and-2-kno</item><item key="geo_id_plat">E-GEOD-50822_A-AFFY-45</item><item key="name">Differential neuronal targeting of a new and 2 known calcium channel &#946;4 subunit splice variants correlates with their regulation of gene expression</item><item key="created">Nov.12, 2014</item><item key="summary">The &#946; subunits of voltage-gated calcium channels regulate surface expression and gating of CaV1 and CaV2 &#945;1 subunits, and thus contribute to neuronal excitability, neurotransmitter release and calcium-induced gene regulation. In addition certain &#946; subunits are targeted into the nucleus, where they directly interact with the epigenetic machinery. Whereas their involvement in this multitude of functions is reflected by a great molecular heterogeneity of &#946; isoforms derived from four genes and abundant alternative splicing, little is known about the roles of individual &#946; variants in specific neuronal functions. In the present study, an alternatively spliced &#946;4 subunit lacking the variable N-terminus (&#946;4e) is identified. It is highly expressed in mouse cerebellum and cultured cerebellar granule cells (CGC) and modulates P/Q-type calcium currents in tsA cells and CaV2.1 surface expression in neurons. Compared to the other two known full-length &#946;4 variants (&#946;4a, &#946;4b) &#946;4e is most abundantly expressed in the distal axon, but lacks nuclear targeting properties. To examine the importance of nuclear targeting of &#946;4 subunits for transcriptional regulation, we performed whole genome expression profiling of CGCs from lethargic mice individually reconstituted with &#946;4a, &#946;4b, and &#946;4e. Notably, the number of genes regulated by each &#946;4 splice variant correlated with the rank order of their nuclear targeting properties (&#946;4b&gt; &#946;4a&gt; &#946;4e). Together these findings support isoform-specific functions of &#946;4 splice variant in neurons, with &#946;4b playing a dual role in channel modulation and gene regulation, while the newly detected &#946;4e variant serves exclusively in calcium channel-dependent functions. We used microarrays to identify gene expression changes caused by &#946;4 splice variants (&#946;4a, &#946;4b and &#946;4e) of the voltage gated calcium channel in cultured cerebellar granule cells of lethargic mice Cultured cerebellar granule cells from lethargic (129/SvJ background) mice reconstituted with the &#946;4 splice variants (&#946;4a, &#946;4b and &#946;4e) were compared to eGFP transfected controls</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-50822</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-50822/samples/</item></data></biogps>
