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The Journal of Neuroscience, November 1, 2001, 21(21):8495-8504

Dominant-Negative Synthesis Suppression of Voltage-Gated Calcium Channel Cav2.2 Induced by Truncated Constructs

Ayesha Raghib, Federica Bertaso, Anthony Davies, Karen M. Page, Alon Meir, Yuri Bogdanov, and Annette C. Dolphin

Department of Pharmacology, University College London, London WC1E6BT, United Kingdom

Voltage-gated calcium channel alpha 1 subunits consist of four domains (I-IV), each with six transmembrane segments. A number of truncated isoforms have been identified to occur as a result of alternative splicing or mutation. We have examined the functional consequences for expression of full-length Cav2.2 (alpha 1B) of its coexpression with truncated constructs of Cav2.2. Domains I-II or domains III-IV, when expressed individually, together with the accessory subunits beta 1b and alpha 2delta -1, did not form functional channels. When they were coexpressed, low-density whole-cell currents and functional channels with properties similar to wild-type channels were observed. However, when domain I-II, domain III-IV, or domain I alone were coexpressed with full-length Cav2.2, they markedly suppressed its functional expression, although at the single channel level, when channels were recorded, there were no differences in their biophysical properties. Furthermore, when it was coexpressed with either domain I-II or domain I, the fluorescence of green fluorescent protein (GFP)-Cav2.2 and expression of Cav2.2 protein was almost abolished. Suppression does not involve sequestration of the Cavbeta subunit, because loss of GFP-Cav2.2 expression also occurred in the absence of beta  subunit, and the effect of domain I-II or domain I could not be mimicked by the cytoplasmic I-II loop of Cav2.2. It requires transmembrane segments, because the isolated Cav2.2 N terminus did not have any effect. Our results indicate that the mechanism of suppression of Cav2.2 by truncated constructs containing domain I involves inhibition of channel synthesis, which may represent a role of endogenously expressed truncated Cav isoforms.

Key words: calcium channel; truncation; expression; suppression; protein synthesis; GFP


Copyright © 2001 Society for Neuroscience  0270-6474/01/21218495-10$05.00/0


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