Cargando…

Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis

Myosin motors are essential players in secretory vesicle trafficking and exocytosis in yeast and mammalian cells; however, similar roles in plants remain a matter for debate, at least for diffusely growing cells. Here, we demonstrate that Arabidopsis (Arabidopsis thaliana) myosin XIK, via its globul...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Weiwei, Huang, Lei, Zhang, Chunhua, Staiger, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8364239/
https://www.ncbi.nlm.nih.gov/pubmed/33871640
http://dx.doi.org/10.1093/plcell/koab116
_version_ 1783738493226188800
author Zhang, Weiwei
Huang, Lei
Zhang, Chunhua
Staiger, Christopher J.
author_facet Zhang, Weiwei
Huang, Lei
Zhang, Chunhua
Staiger, Christopher J.
author_sort Zhang, Weiwei
collection PubMed
description Myosin motors are essential players in secretory vesicle trafficking and exocytosis in yeast and mammalian cells; however, similar roles in plants remain a matter for debate, at least for diffusely growing cells. Here, we demonstrate that Arabidopsis (Arabidopsis thaliana) myosin XIK, via its globular tail domain (GTD), participates in the vesicle tethering step of exocytosis through direct interactions with the exocyst complex. Specifically, myosin XIK GTD bound directly to several exocyst subunits in vitro and functional fluorescently tagged XIK colocalized with multiple exocyst subunits at plasma membrane (PM)-associated stationary foci. Moreover, genetic and pharmacological inhibition of myosin XI activity reduced the rate of appearance and lifetime of stationary exocyst complexes at the PM. By tracking single exocytosis events of cellulose synthase (CESA) complexes with high spatiotemporal resolution imaging and pair-wise colocalization of myosin XIK, exocyst subunits, and CESA6, we demonstrated that XIK associates with secretory vesicles earlier than exocyst and is required for the efficient localization and normal dynamic behavior of exocyst complex at the PM tethering site. This study reveals an important functional role for myosin XI in secretion and provides insights about the dynamic regulation of exocytosis in plants.
format Online
Article
Text
id pubmed-8364239
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-83642392021-08-17 Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis Zhang, Weiwei Huang, Lei Zhang, Chunhua Staiger, Christopher J. Plant Cell Research Articles Myosin motors are essential players in secretory vesicle trafficking and exocytosis in yeast and mammalian cells; however, similar roles in plants remain a matter for debate, at least for diffusely growing cells. Here, we demonstrate that Arabidopsis (Arabidopsis thaliana) myosin XIK, via its globular tail domain (GTD), participates in the vesicle tethering step of exocytosis through direct interactions with the exocyst complex. Specifically, myosin XIK GTD bound directly to several exocyst subunits in vitro and functional fluorescently tagged XIK colocalized with multiple exocyst subunits at plasma membrane (PM)-associated stationary foci. Moreover, genetic and pharmacological inhibition of myosin XI activity reduced the rate of appearance and lifetime of stationary exocyst complexes at the PM. By tracking single exocytosis events of cellulose synthase (CESA) complexes with high spatiotemporal resolution imaging and pair-wise colocalization of myosin XIK, exocyst subunits, and CESA6, we demonstrated that XIK associates with secretory vesicles earlier than exocyst and is required for the efficient localization and normal dynamic behavior of exocyst complex at the PM tethering site. This study reveals an important functional role for myosin XI in secretion and provides insights about the dynamic regulation of exocytosis in plants. Oxford University Press 2021-04-19 /pmc/articles/PMC8364239/ /pubmed/33871640 http://dx.doi.org/10.1093/plcell/koab116 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Articles
Zhang, Weiwei
Huang, Lei
Zhang, Chunhua
Staiger, Christopher J.
Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis
title Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis
title_full Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis
title_fullStr Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis
title_full_unstemmed Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis
title_short Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis
title_sort arabidopsis myosin xik interacts with the exocyst complex to facilitate vesicle tethering during exocytosis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8364239/
https://www.ncbi.nlm.nih.gov/pubmed/33871640
http://dx.doi.org/10.1093/plcell/koab116
work_keys_str_mv AT zhangweiwei arabidopsismyosinxikinteractswiththeexocystcomplextofacilitatevesicletetheringduringexocytosis
AT huanglei arabidopsismyosinxikinteractswiththeexocystcomplextofacilitatevesicletetheringduringexocytosis
AT zhangchunhua arabidopsismyosinxikinteractswiththeexocystcomplextofacilitatevesicletetheringduringexocytosis
AT staigerchristopherj arabidopsismyosinxikinteractswiththeexocystcomplextofacilitatevesicletetheringduringexocytosis