The L-type calcium channel alpha 1C subunit gene undergoes extensive, uncoordinated alternative splicing

The alpha1C subunit is the pore-forming protein for the L-type calcium channel. Previous studies indicate that there is possible tissue-specific alternative splicing of this gene. In this study we cloned the entire open reading frame of the alpha1C subunit cDNA from adult rat cardiac myocytes in a s...

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Veröffentlicht in:Molecular and cellular biochemistry 2005-01, Vol.269 (1-2), p.153-163
Hauptverfasser: Fan, Q Ivy, Vanderpool, Kathleen M, Chung, Hui-San, Marsh, James D
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container_title Molecular and cellular biochemistry
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creator Fan, Q Ivy
Vanderpool, Kathleen M
Chung, Hui-San
Marsh, James D
description The alpha1C subunit is the pore-forming protein for the L-type calcium channel. Previous studies indicate that there is possible tissue-specific alternative splicing of this gene. In this study we cloned the entire open reading frame of the alpha1C subunit cDNA from adult rat cardiac myocytes in a single piece (6.64 kb). Using 75 positive clones that were identified by restriction enzyme mapping, we tested the alternative splicing patterns of the Ca(v) 1.2 gene that encodes the alpha1C subunit protein and focused on five loci: IS6, post-IS6, IIIS2, IVS3, and the c-terminus. The results indicate that: (1) alternative splicing occurs in most of the loci, giving rise to two or three different isoforms at those sites; (2) there is a predominant form for each splicing site, (3) there does not appear to be consistent coordination of splicing at multiple loci of this gene. Alternative splicing is not tissue-specific in most regions.
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subjects Alternative Splicing
Animals
Calcium channels
Calcium Channels, L-Type - genetics
Cloning, Molecular
Gene expression
Male
Myocytes, Cardiac - metabolism
Protein Isoforms - genetics
Protein Structure, Tertiary
Proteins
Rats
Rats, Sprague-Dawley
Restriction Mapping
RNA Splice Sites
RNA, Messenger - metabolism
Tissue Distribution
title The L-type calcium channel alpha 1C subunit gene undergoes extensive, uncoordinated alternative splicing
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