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Interplay of the nuclear envelope with chromatin in physiology and pathology
The nuclear envelope compartmentalizes chromatin in eukaryotic cells. The main nuclear envelope components are lamins that associate with a panoply of factors, including the LEM domain proteins. The nuclear envelope of mammalian cells opens up during cell division. It is reassembled and associated w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529417/ https://www.ncbi.nlm.nih.gov/pubmed/32835589 http://dx.doi.org/10.1080/19491034.2020.1806661 |
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author | Burla, Romina La Torre, Mattia Maccaroni, Klizia Verni, Fiammetta Giunta, Simona Saggio, Isabella |
author_facet | Burla, Romina La Torre, Mattia Maccaroni, Klizia Verni, Fiammetta Giunta, Simona Saggio, Isabella |
author_sort | Burla, Romina |
collection | PubMed |
description | The nuclear envelope compartmentalizes chromatin in eukaryotic cells. The main nuclear envelope components are lamins that associate with a panoply of factors, including the LEM domain proteins. The nuclear envelope of mammalian cells opens up during cell division. It is reassembled and associated with chromatin at the end of mitosis when telomeres tether to the nuclear periphery. Lamins, LEM domain proteins, and DNA binding factors, as BAF, contribute to the reorganization of chromatin. In this context, an emerging role is that of the ESCRT complex, a machinery operating in multiple membrane assembly pathways, including nuclear envelope reformation. Research in this area is unraveling how, mechanistically, ESCRTs link to nuclear envelope associated factors as LEM domain proteins. Importantly, ESCRTs work also during interphase for repairing nuclear envelope ruptures. Altogether the advances in this field are giving new clues for the interpretation of diseases implicating nuclear envelope fragility, as laminopathies and cancer. ABBREVIATIONS: na, not analyzed; ko, knockout; kd, knockdown; NE, nuclear envelope; LEM, LAP2-emerin-MAN1 (LEM)-domain containing proteins; LINC, linker of nucleoskeleton and cytoskeleton complexes; Cyt, cytoplasm; Chr, chromatin; MB, midbody; End, endosomes; Tel, telomeres; INM, inner nuclear membrane; NP, nucleoplasm; NPC, Nuclear Pore Complex; ER, Endoplasmic Reticulum; SPB, spindle pole body. |
format | Online Article Text |
id | pubmed-7529417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-75294172020-10-13 Interplay of the nuclear envelope with chromatin in physiology and pathology Burla, Romina La Torre, Mattia Maccaroni, Klizia Verni, Fiammetta Giunta, Simona Saggio, Isabella Nucleus Review The nuclear envelope compartmentalizes chromatin in eukaryotic cells. The main nuclear envelope components are lamins that associate with a panoply of factors, including the LEM domain proteins. The nuclear envelope of mammalian cells opens up during cell division. It is reassembled and associated with chromatin at the end of mitosis when telomeres tether to the nuclear periphery. Lamins, LEM domain proteins, and DNA binding factors, as BAF, contribute to the reorganization of chromatin. In this context, an emerging role is that of the ESCRT complex, a machinery operating in multiple membrane assembly pathways, including nuclear envelope reformation. Research in this area is unraveling how, mechanistically, ESCRTs link to nuclear envelope associated factors as LEM domain proteins. Importantly, ESCRTs work also during interphase for repairing nuclear envelope ruptures. Altogether the advances in this field are giving new clues for the interpretation of diseases implicating nuclear envelope fragility, as laminopathies and cancer. ABBREVIATIONS: na, not analyzed; ko, knockout; kd, knockdown; NE, nuclear envelope; LEM, LAP2-emerin-MAN1 (LEM)-domain containing proteins; LINC, linker of nucleoskeleton and cytoskeleton complexes; Cyt, cytoplasm; Chr, chromatin; MB, midbody; End, endosomes; Tel, telomeres; INM, inner nuclear membrane; NP, nucleoplasm; NPC, Nuclear Pore Complex; ER, Endoplasmic Reticulum; SPB, spindle pole body. Taylor & Francis 2020-08-23 /pmc/articles/PMC7529417/ /pubmed/32835589 http://dx.doi.org/10.1080/19491034.2020.1806661 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Burla, Romina La Torre, Mattia Maccaroni, Klizia Verni, Fiammetta Giunta, Simona Saggio, Isabella Interplay of the nuclear envelope with chromatin in physiology and pathology |
title | Interplay of the nuclear envelope with chromatin in physiology and pathology |
title_full | Interplay of the nuclear envelope with chromatin in physiology and pathology |
title_fullStr | Interplay of the nuclear envelope with chromatin in physiology and pathology |
title_full_unstemmed | Interplay of the nuclear envelope with chromatin in physiology and pathology |
title_short | Interplay of the nuclear envelope with chromatin in physiology and pathology |
title_sort | interplay of the nuclear envelope with chromatin in physiology and pathology |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529417/ https://www.ncbi.nlm.nih.gov/pubmed/32835589 http://dx.doi.org/10.1080/19491034.2020.1806661 |
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