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Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex

The nuclear pore complex (NPC) is responsible for nucleocytoplasmic transport and constitutes a hub for control of gene expression. The components of NPCs from several eukaryotic lineages have been determined, but only the yeast and vertebrate NPCs have been extensively characterized at the quaterna...

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Autores principales: Obado, Samson O., Brillantes, Marc, Uryu, Kunihiro, Zhang, Wenzhu, Ketaren, Natalia E., Chait, Brian T., Field, Mark C., Rout, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758718/
https://www.ncbi.nlm.nih.gov/pubmed/26891179
http://dx.doi.org/10.1371/journal.pbio.1002365
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author Obado, Samson O.
Brillantes, Marc
Uryu, Kunihiro
Zhang, Wenzhu
Ketaren, Natalia E.
Chait, Brian T.
Field, Mark C.
Rout, Michael P.
author_facet Obado, Samson O.
Brillantes, Marc
Uryu, Kunihiro
Zhang, Wenzhu
Ketaren, Natalia E.
Chait, Brian T.
Field, Mark C.
Rout, Michael P.
author_sort Obado, Samson O.
collection PubMed
description The nuclear pore complex (NPC) is responsible for nucleocytoplasmic transport and constitutes a hub for control of gene expression. The components of NPCs from several eukaryotic lineages have been determined, but only the yeast and vertebrate NPCs have been extensively characterized at the quaternary level. Significantly, recent evidence indicates that compositional similarity does not necessarily correspond to homologous architecture between NPCs from different taxa. To address this, we describe the interactome of the trypanosome NPC, a representative, highly divergent eukaryote. We identify numerous new NPC components and report an exhaustive interactome, allowing assignment of trypanosome nucleoporins to discrete NPC substructures. Remarkably, despite retaining similar protein composition, there are exceptional architectural dissimilarities between opisthokont (yeast and vertebrates) and excavate (trypanosomes) NPCs. Whilst elements of the inner core are conserved, numerous peripheral structures are highly divergent, perhaps reflecting requirements to interface with divergent nuclear and cytoplasmic functions. Moreover, the trypanosome NPC has almost complete nucleocytoplasmic symmetry, in contrast to the opisthokont NPC; this may reflect divergence in RNA export processes at the NPC cytoplasmic face, as we find evidence supporting Ran-dependent mRNA export in trypanosomes, similar to protein transport. We propose a model of stepwise acquisition of nucleocytoplasmic mechanistic complexity and demonstrate that detailed dissection of macromolecular complexes provides fuller understanding of evolutionary processes.
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spelling pubmed-47587182016-02-26 Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex Obado, Samson O. Brillantes, Marc Uryu, Kunihiro Zhang, Wenzhu Ketaren, Natalia E. Chait, Brian T. Field, Mark C. Rout, Michael P. PLoS Biol Research Article The nuclear pore complex (NPC) is responsible for nucleocytoplasmic transport and constitutes a hub for control of gene expression. The components of NPCs from several eukaryotic lineages have been determined, but only the yeast and vertebrate NPCs have been extensively characterized at the quaternary level. Significantly, recent evidence indicates that compositional similarity does not necessarily correspond to homologous architecture between NPCs from different taxa. To address this, we describe the interactome of the trypanosome NPC, a representative, highly divergent eukaryote. We identify numerous new NPC components and report an exhaustive interactome, allowing assignment of trypanosome nucleoporins to discrete NPC substructures. Remarkably, despite retaining similar protein composition, there are exceptional architectural dissimilarities between opisthokont (yeast and vertebrates) and excavate (trypanosomes) NPCs. Whilst elements of the inner core are conserved, numerous peripheral structures are highly divergent, perhaps reflecting requirements to interface with divergent nuclear and cytoplasmic functions. Moreover, the trypanosome NPC has almost complete nucleocytoplasmic symmetry, in contrast to the opisthokont NPC; this may reflect divergence in RNA export processes at the NPC cytoplasmic face, as we find evidence supporting Ran-dependent mRNA export in trypanosomes, similar to protein transport. We propose a model of stepwise acquisition of nucleocytoplasmic mechanistic complexity and demonstrate that detailed dissection of macromolecular complexes provides fuller understanding of evolutionary processes. Public Library of Science 2016-02-18 /pmc/articles/PMC4758718/ /pubmed/26891179 http://dx.doi.org/10.1371/journal.pbio.1002365 Text en © 2016 Obado et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Obado, Samson O.
Brillantes, Marc
Uryu, Kunihiro
Zhang, Wenzhu
Ketaren, Natalia E.
Chait, Brian T.
Field, Mark C.
Rout, Michael P.
Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex
title Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex
title_full Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex
title_fullStr Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex
title_full_unstemmed Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex
title_short Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex
title_sort interactome mapping reveals the evolutionary history of the nuclear pore complex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758718/
https://www.ncbi.nlm.nih.gov/pubmed/26891179
http://dx.doi.org/10.1371/journal.pbio.1002365
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