Cargando…
Sec16 alternative splicing dynamically controls COPII transport efficiency
The transport of secretory proteins from the endoplasmic reticulum (ER) to the Golgi depends on COPII-coated vesicles. While the basic principles of the COPII machinery have been identified, it remains largely unknown how COPII transport is regulated to accommodate tissue- or activation-specific dif...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980449/ https://www.ncbi.nlm.nih.gov/pubmed/27492621 http://dx.doi.org/10.1038/ncomms12347 |
_version_ | 1782447455946670080 |
---|---|
author | Wilhelmi, Ilka Kanski, Regina Neumann, Alexander Herdt, Olga Hoff, Florian Jacob, Ralf Preußner, Marco Heyd, Florian |
author_facet | Wilhelmi, Ilka Kanski, Regina Neumann, Alexander Herdt, Olga Hoff, Florian Jacob, Ralf Preußner, Marco Heyd, Florian |
author_sort | Wilhelmi, Ilka |
collection | PubMed |
description | The transport of secretory proteins from the endoplasmic reticulum (ER) to the Golgi depends on COPII-coated vesicles. While the basic principles of the COPII machinery have been identified, it remains largely unknown how COPII transport is regulated to accommodate tissue- or activation-specific differences in cargo load and identity. Here we show that activation-induced alternative splicing of Sec16 controls adaptation of COPII transport to increased secretory cargo upon T-cell activation. Using splice-site blocking morpholinos and CRISPR/Cas9-mediated genome engineering, we show that the number of ER exit sites, COPII dynamics and transport efficiency depend on Sec16 alternative splicing. As the mechanistic basis, we suggest the C-terminal Sec16 domain to be a splicing-controlled protein interaction platform, with individual isoforms showing differential abilities to recruit COPII components. Our work connects the COPII pathway with alternative splicing, adding a new regulatory layer to protein secretion and its adaptation to changing cellular environments. |
format | Online Article Text |
id | pubmed-4980449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49804492016-08-12 Sec16 alternative splicing dynamically controls COPII transport efficiency Wilhelmi, Ilka Kanski, Regina Neumann, Alexander Herdt, Olga Hoff, Florian Jacob, Ralf Preußner, Marco Heyd, Florian Nat Commun Article The transport of secretory proteins from the endoplasmic reticulum (ER) to the Golgi depends on COPII-coated vesicles. While the basic principles of the COPII machinery have been identified, it remains largely unknown how COPII transport is regulated to accommodate tissue- or activation-specific differences in cargo load and identity. Here we show that activation-induced alternative splicing of Sec16 controls adaptation of COPII transport to increased secretory cargo upon T-cell activation. Using splice-site blocking morpholinos and CRISPR/Cas9-mediated genome engineering, we show that the number of ER exit sites, COPII dynamics and transport efficiency depend on Sec16 alternative splicing. As the mechanistic basis, we suggest the C-terminal Sec16 domain to be a splicing-controlled protein interaction platform, with individual isoforms showing differential abilities to recruit COPII components. Our work connects the COPII pathway with alternative splicing, adding a new regulatory layer to protein secretion and its adaptation to changing cellular environments. Nature Publishing Group 2016-08-05 /pmc/articles/PMC4980449/ /pubmed/27492621 http://dx.doi.org/10.1038/ncomms12347 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wilhelmi, Ilka Kanski, Regina Neumann, Alexander Herdt, Olga Hoff, Florian Jacob, Ralf Preußner, Marco Heyd, Florian Sec16 alternative splicing dynamically controls COPII transport efficiency |
title | Sec16 alternative splicing dynamically controls COPII transport efficiency |
title_full | Sec16 alternative splicing dynamically controls COPII transport efficiency |
title_fullStr | Sec16 alternative splicing dynamically controls COPII transport efficiency |
title_full_unstemmed | Sec16 alternative splicing dynamically controls COPII transport efficiency |
title_short | Sec16 alternative splicing dynamically controls COPII transport efficiency |
title_sort | sec16 alternative splicing dynamically controls copii transport efficiency |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980449/ https://www.ncbi.nlm.nih.gov/pubmed/27492621 http://dx.doi.org/10.1038/ncomms12347 |
work_keys_str_mv | AT wilhelmiilka sec16alternativesplicingdynamicallycontrolscopiitransportefficiency AT kanskiregina sec16alternativesplicingdynamicallycontrolscopiitransportefficiency AT neumannalexander sec16alternativesplicingdynamicallycontrolscopiitransportefficiency AT herdtolga sec16alternativesplicingdynamicallycontrolscopiitransportefficiency AT hoffflorian sec16alternativesplicingdynamicallycontrolscopiitransportefficiency AT jacobralf sec16alternativesplicingdynamicallycontrolscopiitransportefficiency AT preußnermarco sec16alternativesplicingdynamicallycontrolscopiitransportefficiency AT heydflorian sec16alternativesplicingdynamicallycontrolscopiitransportefficiency |