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Probing the 3D architecture of the plant nucleus with microscopy approaches: challenges and solutions

The eukaryotic cell nucleus is a central organelle whose architecture determines genome function at multiple levels. Deciphering nuclear organizing principles influencing cellular responses and identity is a timely challenge. Despite many similarities between plant and animal nuclei, plant nuclei pr...

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Autores principales: Dumur, Tao, Duncan, Susan, Graumann, Katja, Desset, Sophie, Randall, Ricardo S, Scheid, Ortrun Mittelsten, Prodanov, Dimiter, Tatout, Christophe, Baroux, Célia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682351/
https://www.ncbi.nlm.nih.gov/pubmed/31362571
http://dx.doi.org/10.1080/19491034.2019.1644592
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author Dumur, Tao
Duncan, Susan
Graumann, Katja
Desset, Sophie
Randall, Ricardo S
Scheid, Ortrun Mittelsten
Prodanov, Dimiter
Tatout, Christophe
Baroux, Célia
author_facet Dumur, Tao
Duncan, Susan
Graumann, Katja
Desset, Sophie
Randall, Ricardo S
Scheid, Ortrun Mittelsten
Prodanov, Dimiter
Tatout, Christophe
Baroux, Célia
author_sort Dumur, Tao
collection PubMed
description The eukaryotic cell nucleus is a central organelle whose architecture determines genome function at multiple levels. Deciphering nuclear organizing principles influencing cellular responses and identity is a timely challenge. Despite many similarities between plant and animal nuclei, plant nuclei present intriguing specificities. Complementary to molecular and biochemical approaches, 3D microscopy is indispensable for resolving nuclear architecture. However, novel solutions are required for capturing cell-specific, sub-nuclear and dynamic processes. We provide a pointer for utilising high-to-super-resolution microscopy and image processing to probe plant nuclear architecture in 3D at the best possible spatial and temporal resolution and at quantitative and cell-specific levels. High-end imaging and image-processing solutions allow the community now to transcend conventional practices and benefit from continuously improving approaches. These promise to deliver a comprehensive, 3D view of plant nuclear architecture and to capture spatial dynamics of the nuclear compartment in relation to cellular states and responses. Abbreviations: 3D and 4D: Three and Four dimensional; AI: Artificial Intelligence; ant: antipodal nuclei (ant); CLSM: Confocal Laser Scanning Microscopy; CTs: Chromosome Territories; DL: Deep Learning; DLIm: Dynamic Live Imaging; ecn: egg nucleus; FACS: Fluorescence-Activated Cell Sorting; FISH: Fluorescent In Situ Hybridization; FP: Fluorescent Proteins (GFP, RFP, CFP, YFP, mCherry); FRAP: Fluorescence Recovery After Photobleaching; GPU: Graphics Processing Unit; KEEs: KNOT Engaged Elements; INTACT: Isolation of Nuclei TAgged in specific Cell Types; LADs: Lamin-Associated Domains; ML: Machine Learning; NA: Numerical Aperture; NADs: Nucleolar Associated Domains; PALM: Photo-Activated Localization Microscopy; Pixel: Picture element; pn: polar nuclei; PSF: Point Spread Function; RHF: Relative Heterochromatin Fraction; SIM: Structured Illumination Microscopy; SLIm: Static Live Imaging; SMC: Spore Mother Cell; SNR: Signal to Noise Ratio; SRM: Super-Resolution Microscopy; STED: STimulated Emission Depletion; STORM: STochastic Optical Reconstruction Microscopy; syn: synergid nuclei; TADs: Topologically Associating Domains; Voxel: Volumetric pixel
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spelling pubmed-66823512019-08-14 Probing the 3D architecture of the plant nucleus with microscopy approaches: challenges and solutions Dumur, Tao Duncan, Susan Graumann, Katja Desset, Sophie Randall, Ricardo S Scheid, Ortrun Mittelsten Prodanov, Dimiter Tatout, Christophe Baroux, Célia Nucleus Society for Experimental Biology Meeting The eukaryotic cell nucleus is a central organelle whose architecture determines genome function at multiple levels. Deciphering nuclear organizing principles influencing cellular responses and identity is a timely challenge. Despite many similarities between plant and animal nuclei, plant nuclei present intriguing specificities. Complementary to molecular and biochemical approaches, 3D microscopy is indispensable for resolving nuclear architecture. However, novel solutions are required for capturing cell-specific, sub-nuclear and dynamic processes. We provide a pointer for utilising high-to-super-resolution microscopy and image processing to probe plant nuclear architecture in 3D at the best possible spatial and temporal resolution and at quantitative and cell-specific levels. High-end imaging and image-processing solutions allow the community now to transcend conventional practices and benefit from continuously improving approaches. These promise to deliver a comprehensive, 3D view of plant nuclear architecture and to capture spatial dynamics of the nuclear compartment in relation to cellular states and responses. Abbreviations: 3D and 4D: Three and Four dimensional; AI: Artificial Intelligence; ant: antipodal nuclei (ant); CLSM: Confocal Laser Scanning Microscopy; CTs: Chromosome Territories; DL: Deep Learning; DLIm: Dynamic Live Imaging; ecn: egg nucleus; FACS: Fluorescence-Activated Cell Sorting; FISH: Fluorescent In Situ Hybridization; FP: Fluorescent Proteins (GFP, RFP, CFP, YFP, mCherry); FRAP: Fluorescence Recovery After Photobleaching; GPU: Graphics Processing Unit; KEEs: KNOT Engaged Elements; INTACT: Isolation of Nuclei TAgged in specific Cell Types; LADs: Lamin-Associated Domains; ML: Machine Learning; NA: Numerical Aperture; NADs: Nucleolar Associated Domains; PALM: Photo-Activated Localization Microscopy; Pixel: Picture element; pn: polar nuclei; PSF: Point Spread Function; RHF: Relative Heterochromatin Fraction; SIM: Structured Illumination Microscopy; SLIm: Static Live Imaging; SMC: Spore Mother Cell; SNR: Signal to Noise Ratio; SRM: Super-Resolution Microscopy; STED: STimulated Emission Depletion; STORM: STochastic Optical Reconstruction Microscopy; syn: synergid nuclei; TADs: Topologically Associating Domains; Voxel: Volumetric pixel Taylor & Francis 2019-07-30 /pmc/articles/PMC6682351/ /pubmed/31362571 http://dx.doi.org/10.1080/19491034.2019.1644592 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Society for Experimental Biology Meeting
Dumur, Tao
Duncan, Susan
Graumann, Katja
Desset, Sophie
Randall, Ricardo S
Scheid, Ortrun Mittelsten
Prodanov, Dimiter
Tatout, Christophe
Baroux, Célia
Probing the 3D architecture of the plant nucleus with microscopy approaches: challenges and solutions
title Probing the 3D architecture of the plant nucleus with microscopy approaches: challenges and solutions
title_full Probing the 3D architecture of the plant nucleus with microscopy approaches: challenges and solutions
title_fullStr Probing the 3D architecture of the plant nucleus with microscopy approaches: challenges and solutions
title_full_unstemmed Probing the 3D architecture of the plant nucleus with microscopy approaches: challenges and solutions
title_short Probing the 3D architecture of the plant nucleus with microscopy approaches: challenges and solutions
title_sort probing the 3d architecture of the plant nucleus with microscopy approaches: challenges and solutions
topic Society for Experimental Biology Meeting
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682351/
https://www.ncbi.nlm.nih.gov/pubmed/31362571
http://dx.doi.org/10.1080/19491034.2019.1644592
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