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Evolution and diversification of the nuclear pore complex

The nuclear pore complex (NPC) is responsible for transport between the cytoplasm and nucleoplasm and one of the more intricate structures of eukaryotic cells. Typically composed of over 300 polypeptides, the NPC shares evolutionary origins with endo-membrane and intraflagellar transport system comp...

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Autores principales: Makarov, Alexandr A., Padilla-Mejia, Norma E., Field, Mark C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421043/
https://www.ncbi.nlm.nih.gov/pubmed/34282823
http://dx.doi.org/10.1042/BST20200570
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author Makarov, Alexandr A.
Padilla-Mejia, Norma E.
Field, Mark C.
author_facet Makarov, Alexandr A.
Padilla-Mejia, Norma E.
Field, Mark C.
author_sort Makarov, Alexandr A.
collection PubMed
description The nuclear pore complex (NPC) is responsible for transport between the cytoplasm and nucleoplasm and one of the more intricate structures of eukaryotic cells. Typically composed of over 300 polypeptides, the NPC shares evolutionary origins with endo-membrane and intraflagellar transport system complexes. The modern NPC was fully established by the time of the last eukaryotic common ancestor and, hence, prior to eukaryote diversification. Despite the complexity, the NPC structure is surprisingly flexible with considerable variation between lineages. Here, we review diversification of the NPC in major taxa in view of recent advances in genomic and structural characterisation of plant, protist and nucleomorph NPCs and discuss the implications for NPC evolution. Furthermore, we highlight these changes in the context of mRNA export and consider how this process may have influenced NPC diversity. We reveal the NPC as a platform for continual evolution and adaptation.
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spelling pubmed-84210432021-09-14 Evolution and diversification of the nuclear pore complex Makarov, Alexandr A. Padilla-Mejia, Norma E. Field, Mark C. Biochem Soc Trans Review Articles The nuclear pore complex (NPC) is responsible for transport between the cytoplasm and nucleoplasm and one of the more intricate structures of eukaryotic cells. Typically composed of over 300 polypeptides, the NPC shares evolutionary origins with endo-membrane and intraflagellar transport system complexes. The modern NPC was fully established by the time of the last eukaryotic common ancestor and, hence, prior to eukaryote diversification. Despite the complexity, the NPC structure is surprisingly flexible with considerable variation between lineages. Here, we review diversification of the NPC in major taxa in view of recent advances in genomic and structural characterisation of plant, protist and nucleomorph NPCs and discuss the implications for NPC evolution. Furthermore, we highlight these changes in the context of mRNA export and consider how this process may have influenced NPC diversity. We reveal the NPC as a platform for continual evolution and adaptation. Portland Press Ltd. 2021-08-27 2021-07-20 /pmc/articles/PMC8421043/ /pubmed/34282823 http://dx.doi.org/10.1042/BST20200570 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Articles
Makarov, Alexandr A.
Padilla-Mejia, Norma E.
Field, Mark C.
Evolution and diversification of the nuclear pore complex
title Evolution and diversification of the nuclear pore complex
title_full Evolution and diversification of the nuclear pore complex
title_fullStr Evolution and diversification of the nuclear pore complex
title_full_unstemmed Evolution and diversification of the nuclear pore complex
title_short Evolution and diversification of the nuclear pore complex
title_sort evolution and diversification of the nuclear pore complex
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421043/
https://www.ncbi.nlm.nih.gov/pubmed/34282823
http://dx.doi.org/10.1042/BST20200570
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