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ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals

Neurons face unique transport challenges. They need to deliver cargo over long axonal distances and to many presynaptic nerve terminals. Rab GTPases are master regulators of vesicular traffic, but essential presynaptic Rabs have not been identified. Here, we find that Rab6, a Golgi-derived GTPase fo...

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Autores principales: Nyitrai, Hajnalka, Wang, Shan Shan H., Kaeser, Pascal S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360120/
https://www.ncbi.nlm.nih.gov/pubmed/32521280
http://dx.doi.org/10.1016/j.celrep.2020.107712
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author Nyitrai, Hajnalka
Wang, Shan Shan H.
Kaeser, Pascal S.
author_facet Nyitrai, Hajnalka
Wang, Shan Shan H.
Kaeser, Pascal S.
author_sort Nyitrai, Hajnalka
collection PubMed
description Neurons face unique transport challenges. They need to deliver cargo over long axonal distances and to many presynaptic nerve terminals. Rab GTPases are master regulators of vesicular traffic, but essential presynaptic Rabs have not been identified. Here, we find that Rab6, a Golgi-derived GTPase for constitutive secretion, associates with mobile axonal cargo and localizes to nerve terminals. ELKS1 is a stationary presynaptic protein with Golgin homology that binds to Rab6. Knockout and rescue experiments for ELKS1 and Rab6 establish that ELKS1 captures Rab6 cargo. The ELKS1-Rab6-capturing mechanism can be transferred to mitochondria by mistargeting ELKS1 or Rab6 to them. We conclude that nerve terminals have repurposed mechanisms from constitutive exocytosis for their highly regulated secretion. By employing Golgin-like mechanisms with anchored ELKS extending its coiled-coils to capture Rab6 cargo, they have spatially separated cargo capture from fusion. ELKS complexes connect to active zones and may mediate vesicle progression toward release sites.
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spelling pubmed-73601202020-07-14 ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals Nyitrai, Hajnalka Wang, Shan Shan H. Kaeser, Pascal S. Cell Rep Article Neurons face unique transport challenges. They need to deliver cargo over long axonal distances and to many presynaptic nerve terminals. Rab GTPases are master regulators of vesicular traffic, but essential presynaptic Rabs have not been identified. Here, we find that Rab6, a Golgi-derived GTPase for constitutive secretion, associates with mobile axonal cargo and localizes to nerve terminals. ELKS1 is a stationary presynaptic protein with Golgin homology that binds to Rab6. Knockout and rescue experiments for ELKS1 and Rab6 establish that ELKS1 captures Rab6 cargo. The ELKS1-Rab6-capturing mechanism can be transferred to mitochondria by mistargeting ELKS1 or Rab6 to them. We conclude that nerve terminals have repurposed mechanisms from constitutive exocytosis for their highly regulated secretion. By employing Golgin-like mechanisms with anchored ELKS extending its coiled-coils to capture Rab6 cargo, they have spatially separated cargo capture from fusion. ELKS complexes connect to active zones and may mediate vesicle progression toward release sites. 2020-06-09 /pmc/articles/PMC7360120/ /pubmed/32521280 http://dx.doi.org/10.1016/j.celrep.2020.107712 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license.
spellingShingle Article
Nyitrai, Hajnalka
Wang, Shan Shan H.
Kaeser, Pascal S.
ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals
title ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals
title_full ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals
title_fullStr ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals
title_full_unstemmed ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals
title_short ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals
title_sort elks1 captures rab6-marked vesicular cargo in presynaptic nerve terminals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360120/
https://www.ncbi.nlm.nih.gov/pubmed/32521280
http://dx.doi.org/10.1016/j.celrep.2020.107712
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