Loss of MEC-17 Leads to Microtubule Instability and Axonal Degeneration

Highlights

• Mutations in mec-17 cause spontaneous, adult-onset axonal degeneration

• Loss of MEC-17 affects microtubule dynamics

• Axons lacking MEC-17 function have mitochondrial and transport defects

• MEC-17 axonal protection is independent from acetyltransferase activity

Summary

Axonal degeneration arises as a consequence of neuronal injury and is a common hallmark of a number of neurodegenerative diseases. However, the genetic causes and the cellular mechanisms that trigger this process are still largely unknown. Based on forward genetic screening in C. elegans, we have identified the α-tubulin acetyltransferase gene mec-17 as causing spontaneous, adult-onset, and progressive axonal degeneration. Loss of MEC-17 leads to microtubule instability, a reduction in mitochondrial number, and disrupted axonal transport, with altered distribution of both mitochondria and synaptic components. Furthermore, mec-17-mediated axonal degeneration occurs independently from its acetyltransferase domain; is enhanced by mutation of coel-1, a tubulin-associated molecule; and correlates with the animal’s body length. This study therefore identifies a critical role for the conserved microtubule-associated protein MEC-17 in preserving axon integrity and preventing axonal degeneration.