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Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons.

Published version
Peer-reviewed

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Authors

Mukherjee, Amrita 
Brooks, Paul S 

Abstract

Neurons contain polarised microtubule arrays essential for neuronal function. How microtubule nucleation and polarity are regulated within neurons remains unclear. We show that γ-tubulin localises asymmetrically to the somatic Golgi within Drosophila neurons. Microtubules originate from the Golgi with an initial growth preference towards the axon. Their growing plus ends also turn towards and into the axon, adding to the plus-end-out microtubule pool. Any plus ends that reach a dendrite, however, do not readily enter, maintaining minus-end-out polarity. Both turning towards the axon and exclusion from dendrites depend on Kinesin-2, a plus-end-associated motor that guides growing plus ends along adjacent microtubules. We propose that Kinesin-2 engages with a polarised microtubule network within the soma to guide growing microtubules towards the axon; while at dendrite entry sites engagement with microtubules of opposite polarity generates a backward stalling force that prevents entry into dendrites and thus maintains minus-end-out polarity within proximal dendrites.

Description

Keywords

D. melanogaster, Golgi, Kinesin-2, cell biology, g-turc, microtubules, neurons, neuroscience, polarity, Animals, Cell Polarity, Drosophila Proteins, Drosophila melanogaster, Golgi Apparatus, Kinesins, Larva, Microtubules, Neurons

Journal Title

Elife

Conference Name

Journal ISSN

2050-084X
2050-084X

Volume Title

9

Publisher

eLife Sciences Publications, Ltd
Sponsorship
Wellcome Trust (105653/Z/14/Z)
Isaac Newton Trust (18.23(p))
Biotechnology and Biological Sciences Research Council (BB/P019188/1)
Issac Newton Trust, University of Cambridge