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Critical Role for Cold Shock Protein YB-1 in Cytokinesis

SIMPLE SUMMARY: Y-box-binding protein-1, YB-1, plays an important role in regulating the cell cycle, although precisely how it does the is unknown. Using live cell imaging, we show that YB-1 is essential for initiating the last step of cell division (cytokinesis), required for creation of two daught...

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Autores principales: Mehta, Sunali, Algie, Michael, Al-Jabry, Tariq, McKinney, Cushla, Kannan, Srinivasaraghavan, Verma, Chandra S, Ma, Weini, Zhang, Jessie, Bartolec, Tara K., Masamsetti, V. Pragathi, Parker, Kim, Henderson, Luke, Gould, Maree L, Bhatia, Puja, Harfoot, Rhodri, Chircop, Megan, Kleffmann, Torsten, Cohen, Scott B, Woolley, Adele G, Cesare, Anthony J, Braithwaite, Antony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565962/
https://www.ncbi.nlm.nih.gov/pubmed/32882852
http://dx.doi.org/10.3390/cancers12092473
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author Mehta, Sunali
Algie, Michael
Al-Jabry, Tariq
McKinney, Cushla
Kannan, Srinivasaraghavan
Verma, Chandra S
Ma, Weini
Zhang, Jessie
Bartolec, Tara K.
Masamsetti, V. Pragathi
Parker, Kim
Henderson, Luke
Gould, Maree L
Bhatia, Puja
Harfoot, Rhodri
Chircop, Megan
Kleffmann, Torsten
Cohen, Scott B
Woolley, Adele G
Cesare, Anthony J
Braithwaite, Antony
author_facet Mehta, Sunali
Algie, Michael
Al-Jabry, Tariq
McKinney, Cushla
Kannan, Srinivasaraghavan
Verma, Chandra S
Ma, Weini
Zhang, Jessie
Bartolec, Tara K.
Masamsetti, V. Pragathi
Parker, Kim
Henderson, Luke
Gould, Maree L
Bhatia, Puja
Harfoot, Rhodri
Chircop, Megan
Kleffmann, Torsten
Cohen, Scott B
Woolley, Adele G
Cesare, Anthony J
Braithwaite, Antony
author_sort Mehta, Sunali
collection PubMed
description SIMPLE SUMMARY: Y-box-binding protein-1, YB-1, plays an important role in regulating the cell cycle, although precisely how it does the is unknown. Using live cell imaging, we show that YB-1 is essential for initiating the last step of cell division (cytokinesis), required for creation of two daughter cells. Using confocal microscopy we showed that YB-1 regulates the spatial distribution of key proteins essential for cytokinesis to occur and that this required YB-1 to be phosphorylated on several residues. In-silico modeling demonstrated that modifications at these residues resulted in conformational changes in YB-1 protein allowing it to interact with proteins essential for cytokinesis. As many cancers have high levels YB-1 and these are associated with poor prognosis, our data suggest developing small molecule inhibitors to block YB-1 phosphorylation could be a novel approach to cancer therapy. ABSTRACT: High levels of the cold shock protein Y-box-binding protein-1, YB-1, are tightly correlated with increased cell proliferation and progression. However, the precise mechanism by which YB-1 regulates proliferation is unknown. Here, we found that YB-1 depletion in several cancer cell lines and in immortalized fibroblasts resulted in cytokinesis failure and consequent multinucleation. Rescue experiments indicated that YB-1 was required for completion of cytokinesis. Using confocal imaging we found that YB-1 was essential for orchestrating the spatio-temporal distribution of the microtubules, β-actin and the chromosome passenger complex (CPC) to define the cleavage plane. We show that phosphorylation at six serine residues was essential for cytokinesis, of which novel sites were identified using mass spectrometry. Using atomistic modelling we show how phosphorylation at multiple sites alters YB-1 conformation, allowing it to interact with protein partners. Our results establish phosphorylated YB-1 as a critical regulator of cytokinesis, defining precisely how YB-1 regulates cell division.
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spelling pubmed-75659622020-10-26 Critical Role for Cold Shock Protein YB-1 in Cytokinesis Mehta, Sunali Algie, Michael Al-Jabry, Tariq McKinney, Cushla Kannan, Srinivasaraghavan Verma, Chandra S Ma, Weini Zhang, Jessie Bartolec, Tara K. Masamsetti, V. Pragathi Parker, Kim Henderson, Luke Gould, Maree L Bhatia, Puja Harfoot, Rhodri Chircop, Megan Kleffmann, Torsten Cohen, Scott B Woolley, Adele G Cesare, Anthony J Braithwaite, Antony Cancers (Basel) Article SIMPLE SUMMARY: Y-box-binding protein-1, YB-1, plays an important role in regulating the cell cycle, although precisely how it does the is unknown. Using live cell imaging, we show that YB-1 is essential for initiating the last step of cell division (cytokinesis), required for creation of two daughter cells. Using confocal microscopy we showed that YB-1 regulates the spatial distribution of key proteins essential for cytokinesis to occur and that this required YB-1 to be phosphorylated on several residues. In-silico modeling demonstrated that modifications at these residues resulted in conformational changes in YB-1 protein allowing it to interact with proteins essential for cytokinesis. As many cancers have high levels YB-1 and these are associated with poor prognosis, our data suggest developing small molecule inhibitors to block YB-1 phosphorylation could be a novel approach to cancer therapy. ABSTRACT: High levels of the cold shock protein Y-box-binding protein-1, YB-1, are tightly correlated with increased cell proliferation and progression. However, the precise mechanism by which YB-1 regulates proliferation is unknown. Here, we found that YB-1 depletion in several cancer cell lines and in immortalized fibroblasts resulted in cytokinesis failure and consequent multinucleation. Rescue experiments indicated that YB-1 was required for completion of cytokinesis. Using confocal imaging we found that YB-1 was essential for orchestrating the spatio-temporal distribution of the microtubules, β-actin and the chromosome passenger complex (CPC) to define the cleavage plane. We show that phosphorylation at six serine residues was essential for cytokinesis, of which novel sites were identified using mass spectrometry. Using atomistic modelling we show how phosphorylation at multiple sites alters YB-1 conformation, allowing it to interact with protein partners. Our results establish phosphorylated YB-1 as a critical regulator of cytokinesis, defining precisely how YB-1 regulates cell division. MDPI 2020-09-01 /pmc/articles/PMC7565962/ /pubmed/32882852 http://dx.doi.org/10.3390/cancers12092473 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mehta, Sunali
Algie, Michael
Al-Jabry, Tariq
McKinney, Cushla
Kannan, Srinivasaraghavan
Verma, Chandra S
Ma, Weini
Zhang, Jessie
Bartolec, Tara K.
Masamsetti, V. Pragathi
Parker, Kim
Henderson, Luke
Gould, Maree L
Bhatia, Puja
Harfoot, Rhodri
Chircop, Megan
Kleffmann, Torsten
Cohen, Scott B
Woolley, Adele G
Cesare, Anthony J
Braithwaite, Antony
Critical Role for Cold Shock Protein YB-1 in Cytokinesis
title Critical Role for Cold Shock Protein YB-1 in Cytokinesis
title_full Critical Role for Cold Shock Protein YB-1 in Cytokinesis
title_fullStr Critical Role for Cold Shock Protein YB-1 in Cytokinesis
title_full_unstemmed Critical Role for Cold Shock Protein YB-1 in Cytokinesis
title_short Critical Role for Cold Shock Protein YB-1 in Cytokinesis
title_sort critical role for cold shock protein yb-1 in cytokinesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565962/
https://www.ncbi.nlm.nih.gov/pubmed/32882852
http://dx.doi.org/10.3390/cancers12092473
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