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J Biol Chem ; 276(2): 1398-406, 2001 Jan 12.
Article in English | MEDLINE | ID: mdl-11010971

ABSTRACT

Novel splice variants of the alpha(1) subunit of the Ca(v)1.2 voltage-gated Ca(2+) channel were identified that predicted two truncated forms of the alpha(1) subunit comprising domains I and II generated by alternative splicing in the intracellular loop region linking domains II and III. In rabbit heart splice variant 1 (RH-1), exon 19 was deleted, which resulted in a reading frameshift of exon 20 with a premature termination codon and a novel 19-amino acid carboxyl-terminal tail. In the RH-2 variant, exons 17 and 18 were deleted, leading to a reading frameshift of exons 19 and 20 with a premature stop codon and a novel 62-amino acid carboxyl-terminal tail. RNase protection assays with RH-1 and RH-2 cRNA probes confirmed the expression in cardiac and neuronal tissue but not skeletal muscle. The deduced amino acid sequence from full-length cDNAs encoding the two variants predicted polypeptides of 99.0 and 99.2 kDa, which constituted domains I and II of the alpha(1) subunit of the Ca(v)1.2 channel. Antipeptide antibodies directed to sequences in the second intracellular loop between domains II and III identified the 240-kDa Ca(v)1.2 subunit in sarcolemmal and heavy sarcoplasmic reticulum (HSR) membranes and a 99-kDa polypeptide in the HSR. An antipeptide antibody raised against unique sequences in the RH-2 variant also identified a 99-kDa polypeptide in the HSR. These data reveal the expression of additional Ca(2+) channel structural units generated by alternative splicing of the Ca(v)1.2 gene.


Subject(s)
Calcium Channels, L-Type/chemistry , Calcium Channels, L-Type/genetics , Calcium Channels/chemistry , Calcium Channels/genetics , Alternative Splicing , Amino Acid Sequence , Animals , Base Sequence , Brain/metabolism , Calcium Channels/physiology , Calcium Channels, L-Type/physiology , Cloning, Molecular , DNA, Complementary , Exons , Frameshift Mutation , Genetic Variation , Models, Molecular , Molecular Sequence Data , Muscle, Skeletal/metabolism , Mutagenesis , Myocardium/metabolism , Protein Structure, Secondary , Protein Subunits , Rabbits , Reverse Transcriptase Polymerase Chain Reaction , Sequence Alignment , Sequence Deletion , Sequence Homology, Amino Acid
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