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Mutation of the H12-helix of α-tubulin/MEC-12 disrupts the localization of neuronal mitochondria. | LitMetric

Mutation of the H12-helix of α-tubulin/MEC-12 disrupts the localization of neuronal mitochondria.

MicroPubl Biol

Neuroscience Program, Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology, Monash University, Melbourne VIC 3800 Australia.

Published: October 2022

AI Article Synopsis

Article Abstract

Microtubules are essential components of the cytoskeleton that allow bi-lateral neuronal transport. Correct regulation of these complex intracellular transport processes is central to neuronal function. However, despite major advancements in our knowledge, we still lack a complete understanding on how neuronal transport is regulated. Here, we provide further evidence for the importance of the highly conserved N-terminal H12-helix of α-tubulin. We show that a mutation in this region results in the mistargeting of axonal mitochondria in , thereby establishing the importance of the H12-helix in regulating mitochondrial transport in neurons.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638805PMC
http://dx.doi.org/10.17912/micropub.biology.000659DOI Listing

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