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A time-resolved interaction analysis of Bem1 reconstructs the flow of Cdc42 during polar growth
Cdc42 organizes cellular polarity and directs the formation of cellular structures in many organisms. By locating Cdc24, the source of active Cdc42, to the growing front of the yeast cell, the scaffold protein Bem1, is instrumental in shaping the cellular gradient of Cdc42. This gradient instructs b...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409549/ https://www.ncbi.nlm.nih.gov/pubmed/32737079 http://dx.doi.org/10.26508/lsa.202000813 |
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author | Grinhagens, Sören Dünkler, Alexander Wu, Yehui Rieger, Lucia Brenner, Philipp Gronemeyer, Thomas Mulaw, Medhanie A Johnsson, Nils |
author_facet | Grinhagens, Sören Dünkler, Alexander Wu, Yehui Rieger, Lucia Brenner, Philipp Gronemeyer, Thomas Mulaw, Medhanie A Johnsson, Nils |
author_sort | Grinhagens, Sören |
collection | PubMed |
description | Cdc42 organizes cellular polarity and directs the formation of cellular structures in many organisms. By locating Cdc24, the source of active Cdc42, to the growing front of the yeast cell, the scaffold protein Bem1, is instrumental in shaping the cellular gradient of Cdc42. This gradient instructs bud formation, bud growth, or cytokinesis through the actions of a diverse set of effector proteins. To address how Bem1 participates in these transformations, we systematically tracked its protein interactions during one cell cycle to define the ensemble of Bem1 interaction states for each cell cycle stage. Mutants of Bem1 that interact with only a discrete subset of the interaction partners allowed to assign specific functions to different interaction states and identified the determinants for their cellular distributions. The analysis characterizes Bem1 as a cell cycle–specific shuttle that distributes active Cdc42 from its source to its effectors. It further suggests that Bem1 might convert the PAKs Cla4 and Ste20 into their active conformations. |
format | Online Article Text |
id | pubmed-7409549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-74095492020-08-21 A time-resolved interaction analysis of Bem1 reconstructs the flow of Cdc42 during polar growth Grinhagens, Sören Dünkler, Alexander Wu, Yehui Rieger, Lucia Brenner, Philipp Gronemeyer, Thomas Mulaw, Medhanie A Johnsson, Nils Life Sci Alliance Research Articles Cdc42 organizes cellular polarity and directs the formation of cellular structures in many organisms. By locating Cdc24, the source of active Cdc42, to the growing front of the yeast cell, the scaffold protein Bem1, is instrumental in shaping the cellular gradient of Cdc42. This gradient instructs bud formation, bud growth, or cytokinesis through the actions of a diverse set of effector proteins. To address how Bem1 participates in these transformations, we systematically tracked its protein interactions during one cell cycle to define the ensemble of Bem1 interaction states for each cell cycle stage. Mutants of Bem1 that interact with only a discrete subset of the interaction partners allowed to assign specific functions to different interaction states and identified the determinants for their cellular distributions. The analysis characterizes Bem1 as a cell cycle–specific shuttle that distributes active Cdc42 from its source to its effectors. It further suggests that Bem1 might convert the PAKs Cla4 and Ste20 into their active conformations. Life Science Alliance LLC 2020-07-31 /pmc/articles/PMC7409549/ /pubmed/32737079 http://dx.doi.org/10.26508/lsa.202000813 Text en © 2020 Grinhagens et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Grinhagens, Sören Dünkler, Alexander Wu, Yehui Rieger, Lucia Brenner, Philipp Gronemeyer, Thomas Mulaw, Medhanie A Johnsson, Nils A time-resolved interaction analysis of Bem1 reconstructs the flow of Cdc42 during polar growth |
title | A time-resolved interaction analysis of Bem1 reconstructs the flow of Cdc42 during polar growth |
title_full | A time-resolved interaction analysis of Bem1 reconstructs the flow of Cdc42 during polar growth |
title_fullStr | A time-resolved interaction analysis of Bem1 reconstructs the flow of Cdc42 during polar growth |
title_full_unstemmed | A time-resolved interaction analysis of Bem1 reconstructs the flow of Cdc42 during polar growth |
title_short | A time-resolved interaction analysis of Bem1 reconstructs the flow of Cdc42 during polar growth |
title_sort | time-resolved interaction analysis of bem1 reconstructs the flow of cdc42 during polar growth |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409549/ https://www.ncbi.nlm.nih.gov/pubmed/32737079 http://dx.doi.org/10.26508/lsa.202000813 |
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