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唐氏综合征细胞黏附分子的过表达损害精确的突触靶向。

Overexpression of Down syndrome cell adhesion molecule impairs precise synaptic targeting.

机构信息

Centre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, Québec, Canada.

出版信息

Nat Neurosci. 2013 Jun;16(6):677-82. doi: 10.1038/nn.3396. Epub 2013 May 12.

Abstract

Fragile X syndrome is caused by the loss of Fragile X mental retardation protein (FMRP), an RNA-binding protein that suppresses protein translation. We found that FMRP binds to Down syndrome cell adhesion molecule (Dscam) RNA, a molecule that is involved in neural development and has been implicated in Down syndrome. Elevated Dscam protein levels in FMRP null Drosophila and in flies with three copies of the Dscam gene both produced specific and similar synaptic targeting errors in a hard-wired neural circuit, which impaired the flies' sensory perception. Reducing Dscam levels in FMRP null flies reduced synaptic targeting errors and rescued behavioral responses. Our results indicate that excess Dscam protein may be a common molecular mechanism underlying altered neural wiring in intellectual disabilities such as Fragile X and Down syndromes.

摘要

脆性 X 综合征是由脆性 X 智力低下蛋白(FMRP)缺失引起的,FMRP 是一种 RNA 结合蛋白,可抑制蛋白质翻译。我们发现 FMRP 与唐氏综合征细胞黏附分子(Dscam)RNA 结合,后者参与神经发育,并与唐氏综合征有关。在 FMRP 缺失的果蝇和携带三倍 Dscam 基因的果蝇中,Dscam 蛋白水平升高均导致特定且类似的固定神经回路中的突触靶向错误,从而损害果蝇的感觉感知。减少 FMRP 缺失果蝇中的 Dscam 水平可减少突触靶向错误并挽救行为反应。我们的结果表明,过量的 Dscam 蛋白可能是脆性 X 和唐氏综合征等智力障碍中神经连接改变的常见分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f2/3954815/22d0c912f0dd/nihms3893f1.jpg

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