NORAD orchestrates KLC1-mediated SFPQ transport via liquid-liquid phase separation
Lian, Q.; Han, S.; Chen, H.; Liu, J.; Wang, Y.; Chen, S.; Sun, P.; Jiang, J.; Zhao, R.; Chen, R.; Zhang, X.; Duan, F.; Rong, L.; Yi, W.; Kinghorn, A. B.; Yan, J.; Li, R.; Xia, J.; Qi, Z.; Menasche, G.; Lai, K.-O.; Lai, C. S. W.; Zhou, P.; Huang, J.-D.
Show abstract
Neuronal function requires precise long-distance axonal transport mediated by molecular motors and RNA-binding proteins like SFPQ, though regulatory mechanisms remain poorly defined. We identify long non-coding RNA NORAD as a master regulator of this process through liquid-liquid phase separation (LLPS). While SFPQ and kinesin-1 mediate cargo delivery, the specific RNA coordinating their interaction was unknown. We demonstrate NORAD directly binds kinesin light chain 1 (KLC1) and promotes SFPQ condensation into dynamic LLPS droplets, enabling efficient transport. CRISPR-assisted mapping and functional assays show NORAD depletion disrupts granule dynamics, impairs neuroprotective mRNA localization, and induces axonal degeneration. In vitro reconstitution confirms NORAD-KLC1 synergy enhances SFPQ phase separation, and neuron-specific knockout mice exhibit motor deficits with reduced neuronal density. These findings establish the first evidence of lncRNA NORAD-mediated LLPS in axonal transport, revealing a new paradigm for RNA-guided neuronal maintenance.
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