Lotan I, Goelet P, Gigi A, Dascal N
Division of Physiology and Pharmacology, Sackler School of Medicine, Tel Aviv University, Ramat Aviv, Israel.
Science. 1989 Feb 3;243(4891):666-9. doi: 10.1126/science.2464853.
Although the structure of rabbit skeletal muscle dihydropyridine (DHP) receptor, deduced from cDNA sequence, indicates that this protein is the channel-forming subunit of voltage-dependent calcium channel (VDCC), no functional proof for this prediction has been presented. Two DNA oligonucleotides complementary to DHP-receptor RNA sequences coding for putative membrane-spanning regions of the DHP receptor specifically suppress the expression of the DHP-sensitive VDCC from rabbit and rat heart in Xenopus oocytes. However, these oligonucleotides do not suppress the expression of the DHP-insensitive VDCC and of voltage-dependent sodium and potassium channels. Thus, the gene for DHP receptor of rabbit skeletal muscle is closely related, or identical to, a gene expressed in heart that encodes a component of the DHP-sensitive VDCC. The DHP-sensitive and DHP-insensitive VDCCs are distinct molecular entities.
虽然从cDNA序列推导出来的兔骨骼肌二氢吡啶(DHP)受体结构表明该蛋白质是电压依赖性钙通道(VDCC)的通道形成亚基,但尚未提供支持这一预测的功能证据。两条与编码DHP受体假定跨膜区域的DHP受体RNA序列互补的DNA寡核苷酸,可特异性抑制非洲爪蟾卵母细胞中来自兔和大鼠心脏的DHP敏感型VDCC的表达。然而,这些寡核苷酸并不抑制DHP不敏感型VDCC以及电压依赖性钠通道和钾通道的表达。因此,兔骨骼肌DHP受体基因与心脏中表达的一个基因密切相关或相同,该基因编码DHP敏感型VDCC的一个组分。DHP敏感型和DHP不敏感型VDCC是不同的分子实体。