Back

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.

2026-01-06 molecular biology
10.64898/2026.01.06.697853 bioRxiv
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.

Matching journals

The top 2 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.