Slish D F, Engle D B, Varadi G, Lotan I, Singer D, Dascal N, Schwartz A
Department of Pharmacology and Cell Biophysics, University of Cincinnati College of Medicine, OH 45267-0575.
FEBS Lett. 1989 Jul 3;250(2):509-14. doi: 10.1016/0014-5793(89)80786-0.
Biochemical, pharmacological and electrophysiological evidence implies the existence of tissue specific isoforms of the L-type VDCC. The alpha 1 and alpha 2 subunits of the skeletal muscle calcium channel have been previously cloned and their amino acid sequence deduced. Here we report the isolation and sequencing of a partial cDNA that encodes a heart specific isoform of the alpha 1 subunit. The amino acid sequence deduced from this part cDNA clone shows 64.7% similarity with the skeletal muscle alpha 1 subunit. Northern analysis reveals 2 hybridizing bands, 8.5 and 13 kb, in contrast to one 6.5 kb band in the skeletal muscle. Selective inhibition of mRNA expression in Xenopus oocytes by complementary oligodeoxy-nucleotides derived from the heart clone provides further evidence that the cDNA corresponds to an essential component of the VDCC. These data further support the existence of tissue-specific isoforms of the L-type VDCC.
生化、药理学及电生理学证据表明存在L型电压依赖性钙通道(VDCC)的组织特异性亚型。骨骼肌钙通道的α1和α2亚基此前已被克隆,并推导了它们的氨基酸序列。在此,我们报告了一个编码α1亚基心脏特异性亚型的部分cDNA的分离与测序。从该部分cDNA克隆推导的氨基酸序列与骨骼肌α1亚基显示出64.7%的相似性。Northern分析揭示出两条杂交带,分别为8.5 kb和13 kb,与之形成对比的是,骨骼肌中只有一条6.5 kb的带。源自心脏克隆的互补寡聚脱氧核苷酸对非洲爪蟾卵母细胞中mRNA表达的选择性抑制提供了进一步证据,表明该cDNA对应于VDCC的一个必需组分。这些数据进一步支持了L型VDCC存在组织特异性亚型。