bioRxivMolecular BiologyPreprint
NORAD orchestrates KLC1-mediated SFPQ transport via liquid-liquid phase separation
Shuo HaniD, Huan CheniD, Jiayan Liu, Yang WangiD, Shaoxiang Chen, Panpan Sun, Jing JiangiD, Rubin ZhaoiD, Ruijun CheniD, Xiaoxian Zhang, Fuyu DuaniD, Li RongiD, Wenkai YiiD, Andrew B. KinghorniD, Jian YaniD, Renhao LiiD, JQ Xia, ZhongQuan Qi, Gaël MénaschéiD, Kwok‐On LaiiD, Cora Sau Wan LaiiD, Pengcheng ZhouiD, Jian‐Dong HuangiD, Qizhou LianiD
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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