Cargando…
Pan1 regulates transitions between stages of clathrin-mediated endocytosis
Endocytosis is a well-conserved process by which cells invaginate small portions of the plasma membrane to create vesicles containing extracellular and transmembrane cargo proteins. Dozens of proteins and hundreds of specific binding interactions are needed to coordinate and regulate these events. S...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454182/ https://www.ncbi.nlm.nih.gov/pubmed/25631817 http://dx.doi.org/10.1091/mbc.E14-11-1510 |
_version_ | 1782374569264283648 |
---|---|
author | Bradford, Mary Katherine Whitworth, Karen Wendland, Beverly |
author_facet | Bradford, Mary Katherine Whitworth, Karen Wendland, Beverly |
author_sort | Bradford, Mary Katherine |
collection | PubMed |
description | Endocytosis is a well-conserved process by which cells invaginate small portions of the plasma membrane to create vesicles containing extracellular and transmembrane cargo proteins. Dozens of proteins and hundreds of specific binding interactions are needed to coordinate and regulate these events. Saccharomyces cerevisiae is a powerful model system with which to study clathrin-mediated endocytosis (CME). Pan1 is believed to be a scaffolding protein due to its interactions with numerous proteins that act throughout the endocytic process. Previous research characterized many Pan1 binding interactions, but due to Pan1's essential nature, the exact mechanisms of Pan1's function in endocytosis have been difficult to define. We created a novel Pan1-degron allele, Pan1-AID, in which Pan1 can be specifically and efficiently degraded in <1 h upon addition of the plant hormone auxin. The loss of Pan1 caused a delay in endocytic progression and weakened connections between the coat/actin machinery and the membrane, leading to arrest in CME. In addition, we determined a critical role for the central region of Pan1 in endocytosis and viability. The regions important for endocytosis and viability can be separated, suggesting that Pan1 may have a distinct role in the cell that is essential for viability. |
format | Online Article Text |
id | pubmed-4454182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-44541822015-06-16 Pan1 regulates transitions between stages of clathrin-mediated endocytosis Bradford, Mary Katherine Whitworth, Karen Wendland, Beverly Mol Biol Cell Articles Endocytosis is a well-conserved process by which cells invaginate small portions of the plasma membrane to create vesicles containing extracellular and transmembrane cargo proteins. Dozens of proteins and hundreds of specific binding interactions are needed to coordinate and regulate these events. Saccharomyces cerevisiae is a powerful model system with which to study clathrin-mediated endocytosis (CME). Pan1 is believed to be a scaffolding protein due to its interactions with numerous proteins that act throughout the endocytic process. Previous research characterized many Pan1 binding interactions, but due to Pan1's essential nature, the exact mechanisms of Pan1's function in endocytosis have been difficult to define. We created a novel Pan1-degron allele, Pan1-AID, in which Pan1 can be specifically and efficiently degraded in <1 h upon addition of the plant hormone auxin. The loss of Pan1 caused a delay in endocytic progression and weakened connections between the coat/actin machinery and the membrane, leading to arrest in CME. In addition, we determined a critical role for the central region of Pan1 in endocytosis and viability. The regions important for endocytosis and viability can be separated, suggesting that Pan1 may have a distinct role in the cell that is essential for viability. The American Society for Cell Biology 2015-04-01 /pmc/articles/PMC4454182/ /pubmed/25631817 http://dx.doi.org/10.1091/mbc.E14-11-1510 Text en © 2015 Bradford et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. |
spellingShingle | Articles Bradford, Mary Katherine Whitworth, Karen Wendland, Beverly Pan1 regulates transitions between stages of clathrin-mediated endocytosis |
title | Pan1 regulates transitions between stages of clathrin-mediated endocytosis |
title_full | Pan1 regulates transitions between stages of clathrin-mediated endocytosis |
title_fullStr | Pan1 regulates transitions between stages of clathrin-mediated endocytosis |
title_full_unstemmed | Pan1 regulates transitions between stages of clathrin-mediated endocytosis |
title_short | Pan1 regulates transitions between stages of clathrin-mediated endocytosis |
title_sort | pan1 regulates transitions between stages of clathrin-mediated endocytosis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454182/ https://www.ncbi.nlm.nih.gov/pubmed/25631817 http://dx.doi.org/10.1091/mbc.E14-11-1510 |
work_keys_str_mv | AT bradfordmarykatherine pan1regulatestransitionsbetweenstagesofclathrinmediatedendocytosis AT whitworthkaren pan1regulatestransitionsbetweenstagesofclathrinmediatedendocytosis AT wendlandbeverly pan1regulatestransitionsbetweenstagesofclathrinmediatedendocytosis |