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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2004-11-19
pubmed:abstractText
Low-voltage-activated T-type (Cav3) Ca2+ channels produce low-threshold spikes that trigger burst firing in many neurons. The CACNA1I gene encodes the Cav3.3 isoform, which activates and inactivates much more slowly than the other Cav3 channels. These distinctive kinetic features, along with its brain-region-specific expression, suggest that Cav3.3 channels endow neurons with the ability to generate long-lasting bursts of firing. The human CACNA1I gene contains two regions of alternative splicing: variable inclusion of exon 9 and an alternative acceptor site within exon 33, which leads to deletion of 13 amino acids (Delta33). The goal of this study is to determine the functional consequences of these variations in the full-length channel. The cDNA encoding these regions were cloned using RT-PCR from human brain, and currents were recorded by whole cell patch clamp. Introduction of the Delta33 deletion slowed the rate of channel opening. Addition of exon 9 had little effect on kinetics, whereas its addition to Delta33 channels unexpectedly slowed both activation and inactivation kinetics. Modeling of neuronal firing showed that exon 9 or Delta33 alone reduced burst firing, whereas the combination enhanced firing. The major conclusions of this study are that the intracellular regions after repeats I and IV play a role in channel gating, that their effects are interdependent, suggesting a direct interaction, and that splice variation of Cav3.3 channels provides a mechanism for fine-tuning the latency and duration of low-threshold spikes.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0022-3077
pubmed:author
pubmed:issnType
Print
pubmed:volume
92
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3399-407
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:15254077-Action Potentials, pubmed-meshheading:15254077-Alternative Splicing, pubmed-meshheading:15254077-Amino Acid Sequence, pubmed-meshheading:15254077-Calcium Channels, T-Type, pubmed-meshheading:15254077-Cells, Cultured, pubmed-meshheading:15254077-DNA, Complementary, pubmed-meshheading:15254077-Exons, pubmed-meshheading:15254077-Humans, pubmed-meshheading:15254077-Ion Channel Gating, pubmed-meshheading:15254077-Kidney, pubmed-meshheading:15254077-Membrane Transport Proteins, pubmed-meshheading:15254077-Models, Neurological, pubmed-meshheading:15254077-Molecular Sequence Data, pubmed-meshheading:15254077-Neurons, pubmed-meshheading:15254077-Patch-Clamp Techniques, pubmed-meshheading:15254077-Structure-Activity Relationship, pubmed-meshheading:15254077-Thalamus, pubmed-meshheading:15254077-Transfection
pubmed:year
2004
pubmed:articleTitle
Functional impact of alternative splicing of human T-type Cav3.3 calcium channels.
pubmed:affiliation
Department of Pharmacology, University of Virginia, Charlottesville, Virginia 22908-0735, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.