Zalfa Francesca, Achsel Tilmann, Bagni Claudia
Dipartimento di Biologia, Università di Roma Tor Vergata, Via della Ricerca Scientifica 1, 00133, Roma, Italy.
Curr Opin Neurobiol. 2006 Jun;16(3):265-9. doi: 10.1016/j.conb.2006.05.010. Epub 2006 May 16.
mRNA localization and regulated translation play central roles in neurite outgrowth and synaptic plasticity. A key molecule in these processes is the Fragile X mental retardation protein, FMRP, which is involved in the metabolism of neuronal mRNAs. Absence or mutation of FMRP leads to spine dysmorphogenesis and impairs synaptic plasticity. Studies that have mainly been performed on the mouse and Drosophila models for Fragile X Syndrome showed that FMRP is involved in translational regulation at synapses, but even 15 years after discovery of the FMR1 gene, the precise working mechanisms remain elusive.
信使核糖核酸(mRNA)的定位及翻译调控在神经突生长和突触可塑性中发挥着核心作用。这些过程中的一个关键分子是脆性X智力低下蛋白(FMRP),它参与神经元mRNA的代谢。FMRP的缺失或突变会导致脊柱畸形发生,并损害突触可塑性。主要在脆性X综合征的小鼠和果蝇模型上进行的研究表明,FMRP参与突触处的翻译调控,但即便在FMR1基因被发现15年后,其确切作用机制仍不清楚。