Collin T, Wang J J, Nargeot J, Schwartz A
Department of Pharmacology and Cell Biophysics, University of Cincinnati College of Medicine, OH 45267-0575.
Circ Res. 1993 Jun;72(6):1337-44. doi: 10.1161/01.res.72.6.1337.
We have cloned and sequenced cDNAs for three isoforms of the L-type voltage-dependent calcium channel beta subunit isolated from a normal human heart cDNA library. One of these subunits, designated beta a, hybridized with a 3.4-kb message, and the other two, designated beta b and beta c, hybridized with a message of approximately 1.9 kb. The presence of both of these latter two messages in human heart was confirmed by polymerase chain reaction methodology. Considering the differences between beta a and beta b/beta c, we find it likely that these messages may be encoded by two different gene sequences, beta a and beta b/beta c, and that the beta b/beta c sequence can be alternatively spliced in the 209-260 region. The data suggest that the human heart presents a different pattern of beta subunit expression from that found in the rat and rabbit heart.
我们已从正常人心脏cDNA文库中克隆并测序了L型电压依赖性钙通道β亚基三种同工型的cDNA。其中一个亚基,命名为βa,与一条3.4 kb的信使RNA杂交,另外两个,命名为βb和βc,与一条约1.9 kb的信使RNA杂交。通过聚合酶链反应方法证实了后两种信使RNA在人心脏中的存在。考虑到βa与βb/βc之间的差异,我们发现这些信使RNA可能由两个不同的基因序列βa和βb/βc编码,并且βb/βc序列在209 - 260区域可选择性剪接。数据表明,人心脏呈现出与大鼠和兔心脏不同的β亚基表达模式。