Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut, USA.
Nat Neurosci. 2010 Jul;13(7):819-21. doi: 10.1038/nn.2563. Epub 2010 May 30.
In humans, the absence of Fragile X mental retardation protein (FMRP), an RNA-binding protein, results in Fragile X syndrome, the most common inherited form of intellectual disability. Using biochemical and electrophysiological studies, we found that FMRP binds to the C terminus of the Slack sodium-activated potassium channel to activate the channel in mice. Our findings suggest that Slack activity provides a link between patterns of neuronal firing and changes in protein translation.
在人类中,缺乏 RNA 结合蛋白 Fragile X 智力低下蛋白 (FMRP) 会导致 Fragile X 综合征,这是最常见的遗传性智力残疾形式。通过生化和电生理研究,我们发现 FMRP 与 Slack 钠激活钾通道的 C 末端结合,从而在小鼠中激活该通道。我们的研究结果表明,Slack 活性为神经元放电模式和蛋白质翻译变化之间提供了联系。