Abstract
We have cloned and sequenced a cDNA (rB-α2) encoding an α2 subunit of the voltage-sensitive L-type calcium channel (dihydropyridine receptor) of rat brain. The cDNA (3823 base pairs) encodes a protein of 1091 amino acids with a M(r) of 123,822. The deduced amino acid sequence of rB-α2 cDNA is highly similar (95% amino acid identity) to that of rabbit skeletal muscle α2 subunit. The rB-α2 protein is distinct from the previously cloned skeletal muscle α2-subunit protein [Ellis, S. B., Williams, M. E., Ways, N. R., Brenner, R., Sharp, A. H., Leung, A. T., Campbell, K. P., McKenna, E., Koch, W., Hui, A., Schwartz, A. and Harpold, M. M. (1988) Science 241, 1661- 1664] because it contains an insertion of 7 amino acid residues and a deletion of a 19-amino acid segment between putative transmembrane domains 1 and 2. We show that the rB-α2 and skeletal muscle α2-subunit transcripts are the variants produced by alternative splicing of the primary transcript and that they are differentially expressed in brain and skeletal muscle, respectively.
| Original language | English |
|---|---|
| Pages (from-to) | 3251-3255 |
| Number of pages | 5 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 89 |
| Issue number | 8 |
| DOIs | |
| State | Published - 1992 |
Keywords
- RNA splicing
- in situ hybridization
- ion channel
- primary structure
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