Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Agrawal, Ashutosh, Lele, Tanmay P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2020
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
_version_ 1783588054386081792
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
work_keys_str_mv AT agrawalashutosh geometryofthenuclearenvelopedeterminesitsflexuralstiffness
AT leletanmayp geometryofthenuclearenvelopedeterminesitsflexuralstiffness