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High resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states

How spatial organization of the genome depends on nuclear shape is unknown, mostly because accurate nuclear size and shape measurement is technically challenging. In large cell populations of the yeast Saccharomyces cerevisiae, we assessed the geometry (size and shape) of nuclei in three dimensions...

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Autores principales: Wang, Renjie, Kamgoue, Alain, Normand, Christophe, Léger-Silvestre, Isabelle, Mangeat, Thomas, Gadal, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5201014/
https://www.ncbi.nlm.nih.gov/pubmed/27831493
http://dx.doi.org/10.1242/jcs.188250
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author Wang, Renjie
Kamgoue, Alain
Normand, Christophe
Léger-Silvestre, Isabelle
Mangeat, Thomas
Gadal, Olivier
author_facet Wang, Renjie
Kamgoue, Alain
Normand, Christophe
Léger-Silvestre, Isabelle
Mangeat, Thomas
Gadal, Olivier
author_sort Wang, Renjie
collection PubMed
description How spatial organization of the genome depends on nuclear shape is unknown, mostly because accurate nuclear size and shape measurement is technically challenging. In large cell populations of the yeast Saccharomyces cerevisiae, we assessed the geometry (size and shape) of nuclei in three dimensions with a resolution of 30 nm. We improved an automated fluorescence localization method by implementing a post-acquisition correction of the spherical microscopic aberration along the z-axis, to detect the three dimensional (3D) positions of nuclear pore complexes (NPCs) in the nuclear envelope. Here, we used a method called NucQuant to accurately estimate the geometry of nuclei in 3D throughout the cell cycle. To increase the robustness of the statistics, we aggregated thousands of detected NPCs from a cell population in a single representation using the nucleolus or the spindle pole body (SPB) as references to align nuclei along the same axis. We could detect asymmetric changes of the nucleus associated with modification of nucleolar size. Stereotypical modification of the nucleus toward the nucleolus further confirmed the asymmetric properties of the nuclear envelope.
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spelling pubmed-52010142017-01-23 High resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states Wang, Renjie Kamgoue, Alain Normand, Christophe Léger-Silvestre, Isabelle Mangeat, Thomas Gadal, Olivier J Cell Sci Research Article How spatial organization of the genome depends on nuclear shape is unknown, mostly because accurate nuclear size and shape measurement is technically challenging. In large cell populations of the yeast Saccharomyces cerevisiae, we assessed the geometry (size and shape) of nuclei in three dimensions with a resolution of 30 nm. We improved an automated fluorescence localization method by implementing a post-acquisition correction of the spherical microscopic aberration along the z-axis, to detect the three dimensional (3D) positions of nuclear pore complexes (NPCs) in the nuclear envelope. Here, we used a method called NucQuant to accurately estimate the geometry of nuclei in 3D throughout the cell cycle. To increase the robustness of the statistics, we aggregated thousands of detected NPCs from a cell population in a single representation using the nucleolus or the spindle pole body (SPB) as references to align nuclei along the same axis. We could detect asymmetric changes of the nucleus associated with modification of nucleolar size. Stereotypical modification of the nucleus toward the nucleolus further confirmed the asymmetric properties of the nuclear envelope. The Company of Biologists Ltd 2016-12-15 /pmc/articles/PMC5201014/ /pubmed/27831493 http://dx.doi.org/10.1242/jcs.188250 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Wang, Renjie
Kamgoue, Alain
Normand, Christophe
Léger-Silvestre, Isabelle
Mangeat, Thomas
Gadal, Olivier
High resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states
title High resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states
title_full High resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states
title_fullStr High resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states
title_full_unstemmed High resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states
title_short High resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states
title_sort high resolution microscopy reveals the nuclear shape of budding yeast during cell cycle and in various biological states
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5201014/
https://www.ncbi.nlm.nih.gov/pubmed/27831493
http://dx.doi.org/10.1242/jcs.188250
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