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Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression
Gle2/Rae1 is highly conserved from yeast to humans and has been described as an mRNA export factor. Additionally, it is implicated in the anaphase‐promoting complex‐mediated cell cycle regulation in higher eukaryotes. Here we identify an involvement for Saccharomyces cerevisiae Gle2 in septin organi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472880/ https://www.ncbi.nlm.nih.gov/pubmed/28776765 http://dx.doi.org/10.1002/yea.3249 |
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author | Zander, Gesa Kramer, Wilfried Seel, Anika Krebber, Heike |
author_facet | Zander, Gesa Kramer, Wilfried Seel, Anika Krebber, Heike |
author_sort | Zander, Gesa |
collection | PubMed |
description | Gle2/Rae1 is highly conserved from yeast to humans and has been described as an mRNA export factor. Additionally, it is implicated in the anaphase‐promoting complex‐mediated cell cycle regulation in higher eukaryotes. Here we identify an involvement for Saccharomyces cerevisiae Gle2 in septin organization, which is crucial for cell cycle progression and cell division. Gle2 genetically and physically interacts with components of the septin ring. Importantly, deletion of GLE2 leads to elongated buds, severe defects in septin‐assembly and their cellular mislocalization. Septin‐ring formation is triggered by the septin‐regulating GTPase Cdc42, which establishes and maintains cell polarity. Additionally, activity of the master cell cycle regulator Cdc28 (Cdk1) is needed, which is, besides other functions, also required for G(2)/M‐transition, and in yeast particularly responsible for initiating the apical–isotropic switch. We show genetic and physical interactions of Gle2 with both Cdc42 and Cdc28. Most importantly, we find that gle2∆ severely mislocalizes Cdc42, leading to defects in septin‐complex formation and cell division. Thus, our findings suggest that Gle2 participates in the efficient organization of the septin assembly network, where it might act as a scaffold protein. © 2017 The Authors. Yeast published by John Wiley & Sons, Ltd. |
format | Online Article Text |
id | pubmed-6472880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64728802019-04-24 Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression Zander, Gesa Kramer, Wilfried Seel, Anika Krebber, Heike Yeast Research Articles Gle2/Rae1 is highly conserved from yeast to humans and has been described as an mRNA export factor. Additionally, it is implicated in the anaphase‐promoting complex‐mediated cell cycle regulation in higher eukaryotes. Here we identify an involvement for Saccharomyces cerevisiae Gle2 in septin organization, which is crucial for cell cycle progression and cell division. Gle2 genetically and physically interacts with components of the septin ring. Importantly, deletion of GLE2 leads to elongated buds, severe defects in septin‐assembly and their cellular mislocalization. Septin‐ring formation is triggered by the septin‐regulating GTPase Cdc42, which establishes and maintains cell polarity. Additionally, activity of the master cell cycle regulator Cdc28 (Cdk1) is needed, which is, besides other functions, also required for G(2)/M‐transition, and in yeast particularly responsible for initiating the apical–isotropic switch. We show genetic and physical interactions of Gle2 with both Cdc42 and Cdc28. Most importantly, we find that gle2∆ severely mislocalizes Cdc42, leading to defects in septin‐complex formation and cell division. Thus, our findings suggest that Gle2 participates in the efficient organization of the septin assembly network, where it might act as a scaffold protein. © 2017 The Authors. Yeast published by John Wiley & Sons, Ltd. John Wiley and Sons Inc. 2017-09-28 2017-11 /pmc/articles/PMC6472880/ /pubmed/28776765 http://dx.doi.org/10.1002/yea.3249 Text en © 2017 The Authors. Yeast published by John Wiley & Sons, Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Zander, Gesa Kramer, Wilfried Seel, Anika Krebber, Heike Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression |
title |
Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression |
title_full |
Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression |
title_fullStr |
Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression |
title_full_unstemmed |
Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression |
title_short |
Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression |
title_sort | saccharomyces cerevisiae gle2/rae1 is involved in septin organization, essential for cell cycle progression |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472880/ https://www.ncbi.nlm.nih.gov/pubmed/28776765 http://dx.doi.org/10.1002/yea.3249 |
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