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Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons
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 wi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394546/ https://www.ncbi.nlm.nih.gov/pubmed/32657758 http://dx.doi.org/10.7554/eLife.58943 |
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author | Mukherjee, Amrita Brooks, Paul S Bernard, Fred Guichet, Antoine Conduit, Paul T |
author_facet | Mukherjee, Amrita Brooks, Paul S Bernard, Fred Guichet, Antoine Conduit, Paul T |
author_sort | Mukherjee, Amrita |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7394546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-73945462020-08-03 Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons Mukherjee, Amrita Brooks, Paul S Bernard, Fred Guichet, Antoine Conduit, Paul T eLife Cell Biology 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. eLife Sciences Publications, Ltd 2020-07-13 /pmc/articles/PMC7394546/ /pubmed/32657758 http://dx.doi.org/10.7554/eLife.58943 Text en © 2020, Mukherjee et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Mukherjee, Amrita Brooks, Paul S Bernard, Fred Guichet, Antoine Conduit, Paul T Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons |
title | Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons |
title_full | Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons |
title_fullStr | Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons |
title_full_unstemmed | Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons |
title_short | Microtubules originate asymmetrically at the somatic golgi and are guided via Kinesin2 to maintain polarity within neurons |
title_sort | microtubules originate asymmetrically at the somatic golgi and are guided via kinesin2 to maintain polarity within neurons |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394546/ https://www.ncbi.nlm.nih.gov/pubmed/32657758 http://dx.doi.org/10.7554/eLife.58943 |
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