Source:http://linkedlifedata.com/resource/pubmed/id/15381693
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
48
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pubmed:dateCreated |
2004-11-23
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pubmed:abstractText |
Voltage-gated calcium channels play a major role in many important processes including muscle contraction, neurotransmission, excitation-transcription coupling, and hormone secretion. To date, 10 calcium channel alpha(1)-subunits have been reported, of which four code for L-type calcium channels. In our previous work, we uncovered by transcript-scanning the presence of 19 alternatively spliced exons in the L-type Ca(v)1.2 alpha(1)-subunit. Here, we report the smooth muscle-selective expression of alternatively spliced exon 9(*) in Ca(v)1.2 channels found on arterial smooth muscle. Specific polyclonal antibody against exon 9(*) localized the intense expression of 9(*)-containing Ca(v)1.2 channels on the smooth muscle wall of arteries, but the expression on cardiac muscle was low. Whole-cell patch clamp recordings of the 9(*)-containing Ca(v)1.2 channels in HEK293 cells demonstrated -9 and -11-mV hyperpolarized shift in voltage-dependent activation and current-voltage relationships, respectively. The steady-state inactivation property and sensitivity to blockade by nifedipine of the +/-exon 9(*) splice variants were, however, not significantly different. Such cell-selective expression of an alternatively spliced exon strongly indicates the customization and fine tuning of calcium channel functions through alternative splicing of the pore-forming alpha(1)-subunit. The generation of proteomic variations by alternative splicing of the calcium channel Ca(v)1.2 alpha(1)-subunit can potentially provide a flexible mechanism for muscle or neuronal cells to respond to various physiological signals or to diseases.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
26
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pubmed:volume |
279
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
50329-35
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15381693-Alternative Splicing,
pubmed-meshheading:15381693-Amino Acid Sequence,
pubmed-meshheading:15381693-Antibodies,
pubmed-meshheading:15381693-Blotting, Western,
pubmed-meshheading:15381693-Calcium Channels, L-Type,
pubmed-meshheading:15381693-Electrophysiology,
pubmed-meshheading:15381693-Exons,
pubmed-meshheading:15381693-Humans,
pubmed-meshheading:15381693-Immunohistochemistry,
pubmed-meshheading:15381693-Molecular Sequence Data,
pubmed-meshheading:15381693-Muscle, Smooth
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pubmed:year |
2004
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pubmed:articleTitle |
Smooth muscle-selective alternatively spliced exon generates functional variation in Cav1.2 calcium channels.
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pubmed:affiliation |
National Neuroscience Institute, Singapore 308433.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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