Chang S Y, Yong T F, Yu C Y, Liang M C, Pletnikova O, Troncoso J, Burgunder J-M, Soong T W
Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, 2 Medical Drive, Singapore 117597.
Neuroscience. 2007 Mar 30;145(3):1026-36. doi: 10.1016/j.neuroscience.2006.12.054. Epub 2007 Feb 8.
Ca(v)2.1 Ca(2+) channels (P/Q-type), which participate in various key roles in the CNS by mediating calcium influx, are extensively spliced. One of its alternatively-spliced exons is 37, which forms part of the EF hand. The expression of exon 37a (EFa form), but not exon 37b (EFb form), confers the channel an activity-dependent enhancement of channel opening known as Ca(2+)-dependent facilitation (CDF). In this study, we analyzed the trend of EF hand splice variant distributions in mouse, rat and human brain tissues. We observed a developmental switch in rodents, as well as an age and gender bias in human brain tissues, suggestive of a possible role of these EF hand splice variants in neurophysiological specialization. A parallel study performed on rodent brains showed that the data drawn from human and rodent tissues may not necessarily correlate in the process of aging.
Ca(v)2.1钙离子通道(P/Q型)通过介导钙内流在中枢神经系统中发挥多种关键作用,该通道存在广泛的剪接现象。其一个可变剪接外显子是37,它构成了EF手结构的一部分。外显子37a(EFa形式)而非外显子37b(EFb形式)的表达赋予通道一种依赖于活动的通道开放增强作用,即钙依赖易化(CDF)。在本研究中,我们分析了小鼠、大鼠和人类脑组织中EF手剪接变体分布的趋势。我们观察到啮齿动物存在发育转变,以及人类脑组织存在年龄和性别偏差,这表明这些EF手剪接变体在神经生理特化中可能发挥作用。对啮齿动物大脑进行的一项平行研究表明,来自人类和啮齿动物组织的数据在衰老过程中不一定相关。