C-termini of P/Q-type Ca2+ channel α1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity

Holly B. Kordasiewicz, Randall M. Thompson, H. Brent Clark, Christopher M. Gomez

Research output: Contribution to journalArticlepeer-review

100 Scopus citations

Abstract

P/Q-type voltage-gated calcium channels are regulated, in part, through the cytoplasmic C-terminus of their α1A subunit. Genetic absence or alteration of the C-terminus leads to abnormal channel function and neurological disease. Here, we show that the terminal 60-75 kDa of the endogenous α1A C-terminus is cleaved from the full-length protein and is present in cell nuclei. Antiserum to the C-terminus (CT-2) labels both wild-type mouse and human Purkinje cell nuclei, but not leaner mouse cerebellum. Human embryonic kidney cells stably expressing β3 and α2δ subunits and transiently transfected with full-length human α1A contain a 75 kDa CT-2 reactive peptide in their nuclear fraction. Primary granule cells transfected with C-terminally Green fluorescent protein (GFP)-tagged α1A exhibit GFP nuclear labeling. Nuclear translocation depends partly on the presence of three nuclear localization signals within the C-terminus. The C-terminal fragment bears a polyglutamine tract which, when expanded (Q33) as in spinocerebellar ataxia type 6 (SCA6), is toxic to cells. Moreover, polyglutamine-mediated toxicity is dependent on nuclear localization. Finally, in the absence of flanking sequence, the Q33 expansion alone does not kill cells. These results suggest a novel processing of the P/Q-type calcium channel and a potential mechanism for the pathogenesis of SCA6.

Original languageEnglish (US)
Pages (from-to)1587-1599
Number of pages13
JournalHuman molecular genetics
Volume15
Issue number10
DOIs
StatePublished - May 15 2006

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