Back

Disruption of the PAR3/INSC/LGN complex causes microtubule instability and peripheral neuropathy

Yeh, J.-Y.; Chao, H.-C.; Hung, Y.-C.; Tzou, F.-Y.; Hsiao, C.-T.; Chou, C.-T.; Tsai, Y.-S.; Liao, Y.-C.; Huang, S.-Y.; Kennerson, M.; Lee, Y.-C.; Chan, C.-C.

2023-08-31 neurology
10.1101/2023.08.30.23294746 medRxiv
Show abstract

PAR3/INSC/LGN form an evolutionarily conserved complex required for asymmetric cell division in the developing brain, but its post-developmental function and disease relevance in the peripheral nervous system (PNS) remains unknown. We mapped a new locus for axonal Charcot-Marie-Tooth disease (CMT2) and identified a missense mutation c.209T>G (p.Met70Arg) in the INSC (INSC) gene. Modelling the INSCM70Rvariant in Drosophila, we showed that it caused proprioceptive defects in adult flies, leading to gait defects resembling those in CMT2 patients. Cellularly, PAR3/INSC/LGN dysfunction caused tubulin aggregation and necrotic neurodegeneration, with microtubule-stabilizing agents rescuing both morphological and functional defects of the INSCM70Rmutation in the PNS. Our findings underscore the critical role of the PAR3/INSC/LGN machinery in the adult PNS and highlights a potential therapeutic target for INSC-associated CMT2. One-Sentence SummaryPAR3/INSC/LGN dysfunction causes peripheral neuropathy and is potentially treatable by stabilizing the microtubule network.

Matching journals

The top 7 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.