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STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap
The perinuclear actin cap is an important cytoskeletal structure that regulates nuclear morphology and re-orientation during front-rear polarisation. The mechanisms regulating the actin cap are currently poorly understood. Here, we demonstrate that STEF/TIAM2, a Rac1 selective guanine nucleotide exc...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974301/ https://www.ncbi.nlm.nih.gov/pubmed/29844364 http://dx.doi.org/10.1038/s41467-018-04404-4 |
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author | Woroniuk, Anna Porter, Andrew White, Gavin Newman, Daniel T. Diamantopoulou, Zoi Waring, Thomas Rooney, Claire Strathdee, Douglas Marston, Daniel J. Hahn, Klaus M. Sansom, Owen J. Zech, Tobias Malliri, Angeliki |
author_facet | Woroniuk, Anna Porter, Andrew White, Gavin Newman, Daniel T. Diamantopoulou, Zoi Waring, Thomas Rooney, Claire Strathdee, Douglas Marston, Daniel J. Hahn, Klaus M. Sansom, Owen J. Zech, Tobias Malliri, Angeliki |
author_sort | Woroniuk, Anna |
collection | PubMed |
description | The perinuclear actin cap is an important cytoskeletal structure that regulates nuclear morphology and re-orientation during front-rear polarisation. The mechanisms regulating the actin cap are currently poorly understood. Here, we demonstrate that STEF/TIAM2, a Rac1 selective guanine nucleotide exchange factor, localises at the nuclear envelope, co-localising with the key perinuclear proteins Nesprin-2G and Non-muscle myosin IIB (NMMIIB), where it regulates perinuclear Rac1 activity. We show that STEF depletion reduces apical perinuclear actin cables (a phenotype rescued by targeting active Rac1 to the nuclear envelope), increases nuclear height and impairs nuclear re-orientation. STEF down-regulation also reduces perinuclear pMLC and decreases myosin-generated tension at the nuclear envelope, suggesting that STEF-mediated Rac1 activity regulates NMMIIB activity to promote stabilisation of the perinuclear actin cap. Finally, STEF depletion decreases nuclear stiffness and reduces expression of TAZ-regulated genes, indicating an alteration in mechanosensing pathways as a consequence of disruption of the actin cap. |
format | Online Article Text |
id | pubmed-5974301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59743012018-05-31 STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap Woroniuk, Anna Porter, Andrew White, Gavin Newman, Daniel T. Diamantopoulou, Zoi Waring, Thomas Rooney, Claire Strathdee, Douglas Marston, Daniel J. Hahn, Klaus M. Sansom, Owen J. Zech, Tobias Malliri, Angeliki Nat Commun Article The perinuclear actin cap is an important cytoskeletal structure that regulates nuclear morphology and re-orientation during front-rear polarisation. The mechanisms regulating the actin cap are currently poorly understood. Here, we demonstrate that STEF/TIAM2, a Rac1 selective guanine nucleotide exchange factor, localises at the nuclear envelope, co-localising with the key perinuclear proteins Nesprin-2G and Non-muscle myosin IIB (NMMIIB), where it regulates perinuclear Rac1 activity. We show that STEF depletion reduces apical perinuclear actin cables (a phenotype rescued by targeting active Rac1 to the nuclear envelope), increases nuclear height and impairs nuclear re-orientation. STEF down-regulation also reduces perinuclear pMLC and decreases myosin-generated tension at the nuclear envelope, suggesting that STEF-mediated Rac1 activity regulates NMMIIB activity to promote stabilisation of the perinuclear actin cap. Finally, STEF depletion decreases nuclear stiffness and reduces expression of TAZ-regulated genes, indicating an alteration in mechanosensing pathways as a consequence of disruption of the actin cap. Nature Publishing Group UK 2018-05-29 /pmc/articles/PMC5974301/ /pubmed/29844364 http://dx.doi.org/10.1038/s41467-018-04404-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Woroniuk, Anna Porter, Andrew White, Gavin Newman, Daniel T. Diamantopoulou, Zoi Waring, Thomas Rooney, Claire Strathdee, Douglas Marston, Daniel J. Hahn, Klaus M. Sansom, Owen J. Zech, Tobias Malliri, Angeliki STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap |
title | STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap |
title_full | STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap |
title_fullStr | STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap |
title_full_unstemmed | STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap |
title_short | STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap |
title_sort | stef/tiam2-mediated rac1 activity at the nuclear envelope regulates the perinuclear actin cap |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974301/ https://www.ncbi.nlm.nih.gov/pubmed/29844364 http://dx.doi.org/10.1038/s41467-018-04404-4 |
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