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Geometry of the nuclear envelope determines its flexural stiffness
During closed mitosis in fission yeast, growing microtubules push onto the nuclear envelope to deform it, which results in fission into two daughter nuclei. The resistance of the envelope to bending, quantified by the flexural stiffness, helps determine the microtubule-dependent nuclear shape transf...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521844/ https://www.ncbi.nlm.nih.gov/pubmed/32583742 http://dx.doi.org/10.1091/mbc.E20-02-0163 |
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author | Agrawal, Ashutosh Lele, Tanmay P. |
author_facet | Agrawal, Ashutosh Lele, Tanmay P. |
author_sort | Agrawal, Ashutosh |
collection | PubMed |
description | During closed mitosis in fission yeast, growing microtubules push onto the nuclear envelope to deform it, which results in fission into two daughter nuclei. The resistance of the envelope to bending, quantified by the flexural stiffness, helps determine the microtubule-dependent nuclear shape transformations. Computational models of envelope mechanics have assumed values of the flexural stiffness of the envelope based on simple scaling arguments. The validity of these estimates is in doubt, however, owing to the complex structure of the nuclear envelope. Here, we performed computational analysis of the bending of the nuclear envelope under applied force using a model that accounts for envelope geometry. Our calculations show that the effective bending modulus of the nuclear envelope is an order of magnitude larger than a single membrane and approximately five times greater than the nuclear lamina. This large bending modulus is in part due to the 45 nm separation between the two membranes, which supports larger bending moments in the structure. Further, the effective bending modulus is highly sensitive to the geometry of the nuclear envelope, ranging from twofold to an order magnitude larger than the corresponding single membrane. These results suggest that spatial variations in geometry and mechanical environment of the envelope may cause a spatial distribution of flexural stiffness in the same nucleus. Overall, our calculations support the possibility that the nuclear envelope may balance significant mechanical stresses in yeast and in cells from higher organisms. |
format | Online Article Text |
id | pubmed-7521844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-75218442020-10-06 Geometry of the nuclear envelope determines its flexural stiffness Agrawal, Ashutosh Lele, Tanmay P. Mol Biol Cell Articles During closed mitosis in fission yeast, growing microtubules push onto the nuclear envelope to deform it, which results in fission into two daughter nuclei. The resistance of the envelope to bending, quantified by the flexural stiffness, helps determine the microtubule-dependent nuclear shape transformations. Computational models of envelope mechanics have assumed values of the flexural stiffness of the envelope based on simple scaling arguments. The validity of these estimates is in doubt, however, owing to the complex structure of the nuclear envelope. Here, we performed computational analysis of the bending of the nuclear envelope under applied force using a model that accounts for envelope geometry. Our calculations show that the effective bending modulus of the nuclear envelope is an order of magnitude larger than a single membrane and approximately five times greater than the nuclear lamina. This large bending modulus is in part due to the 45 nm separation between the two membranes, which supports larger bending moments in the structure. Further, the effective bending modulus is highly sensitive to the geometry of the nuclear envelope, ranging from twofold to an order magnitude larger than the corresponding single membrane. These results suggest that spatial variations in geometry and mechanical environment of the envelope may cause a spatial distribution of flexural stiffness in the same nucleus. Overall, our calculations support the possibility that the nuclear envelope may balance significant mechanical stresses in yeast and in cells from higher organisms. The American Society for Cell Biology 2020-07-21 /pmc/articles/PMC7521844/ /pubmed/32583742 http://dx.doi.org/10.1091/mbc.E20-02-0163 Text en © 2020 Agrawal and Lele. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 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. |
spellingShingle | Articles Agrawal, Ashutosh Lele, Tanmay P. Geometry of the nuclear envelope determines its flexural stiffness |
title | Geometry of the nuclear envelope determines its flexural stiffness |
title_full | Geometry of the nuclear envelope determines its flexural stiffness |
title_fullStr | Geometry of the nuclear envelope determines its flexural stiffness |
title_full_unstemmed | Geometry of the nuclear envelope determines its flexural stiffness |
title_short | Geometry of the nuclear envelope determines its flexural stiffness |
title_sort | geometry of the nuclear envelope determines its flexural stiffness |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521844/ https://www.ncbi.nlm.nih.gov/pubmed/32583742 http://dx.doi.org/10.1091/mbc.E20-02-0163 |
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