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Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export

RNA undergoing nuclear export first encounters the basket of the nuclear pore. Two basket proteins, Nup98 and Nup153, are essential for mRNA export, but their molecular partners within the pore are largely unknown. Because the mechanism of RNA export will be in question as long as significant verteb...

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Autores principales: Vasu, Sanjay, Shah, Sundeep, Orjalo, Arturo, Park, Minkyu, Fischer, Wolfgang H., Forbes, Douglass J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150853/
https://www.ncbi.nlm.nih.gov/pubmed/11684705
http://dx.doi.org/10.1083/jcb.200108007
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author Vasu, Sanjay
Shah, Sundeep
Orjalo, Arturo
Park, Minkyu
Fischer, Wolfgang H.
Forbes, Douglass J.
author_facet Vasu, Sanjay
Shah, Sundeep
Orjalo, Arturo
Park, Minkyu
Fischer, Wolfgang H.
Forbes, Douglass J.
author_sort Vasu, Sanjay
collection PubMed
description RNA undergoing nuclear export first encounters the basket of the nuclear pore. Two basket proteins, Nup98 and Nup153, are essential for mRNA export, but their molecular partners within the pore are largely unknown. Because the mechanism of RNA export will be in question as long as significant vertebrate pore proteins remain undiscovered, we set out to find their partners. Fragments of Nup98 and Nup153 were used for pulldown experiments from Xenopus egg extracts, which contain abundant disassembled nuclear pores. Strikingly, Nup98 and Nup153 each bound the same four large proteins. Purification and sequence analysis revealed that two are the known vertebrate nucleoporins, Nup96 and Nup107, whereas two mapped to ORFs of unknown function. The genes encoding the novel proteins were cloned, and antibodies were produced. Immunofluorescence reveals them to be new nucleoporins, designated Nup160 and Nup133, which are accessible on the basket side of the pore. Nucleoporins Nup160, Nup133, Nup107, and Nup96 exist as a complex in Xenopus egg extracts and in assembled pores, now termed the Nup160 complex. Sec13 is prominent in Nup98 and Nup153 pulldowns, and we find it to be a member of the Nup160 complex. We have mapped the sites that are required for binding the Nup160 subcomplex, and have found that in Nup98, the binding site is used to tether Nup98 to the nucleus; in Nup153, the binding site targets Nup153 to the nuclear pore. With transfection and in vivo transport assays, we find that specific Nup160 and Nup133 fragments block poly[A](+) RNA export, but not protein import or export. These results demonstrate that two novel vertebrate nucleoporins, Nup160 and Nup133, not only interact with Nup98 and Nup153, but themselves play a role in mRNA export.
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spelling pubmed-21508532008-05-01 Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export Vasu, Sanjay Shah, Sundeep Orjalo, Arturo Park, Minkyu Fischer, Wolfgang H. Forbes, Douglass J. J Cell Biol Article RNA undergoing nuclear export first encounters the basket of the nuclear pore. Two basket proteins, Nup98 and Nup153, are essential for mRNA export, but their molecular partners within the pore are largely unknown. Because the mechanism of RNA export will be in question as long as significant vertebrate pore proteins remain undiscovered, we set out to find their partners. Fragments of Nup98 and Nup153 were used for pulldown experiments from Xenopus egg extracts, which contain abundant disassembled nuclear pores. Strikingly, Nup98 and Nup153 each bound the same four large proteins. Purification and sequence analysis revealed that two are the known vertebrate nucleoporins, Nup96 and Nup107, whereas two mapped to ORFs of unknown function. The genes encoding the novel proteins were cloned, and antibodies were produced. Immunofluorescence reveals them to be new nucleoporins, designated Nup160 and Nup133, which are accessible on the basket side of the pore. Nucleoporins Nup160, Nup133, Nup107, and Nup96 exist as a complex in Xenopus egg extracts and in assembled pores, now termed the Nup160 complex. Sec13 is prominent in Nup98 and Nup153 pulldowns, and we find it to be a member of the Nup160 complex. We have mapped the sites that are required for binding the Nup160 subcomplex, and have found that in Nup98, the binding site is used to tether Nup98 to the nucleus; in Nup153, the binding site targets Nup153 to the nuclear pore. With transfection and in vivo transport assays, we find that specific Nup160 and Nup133 fragments block poly[A](+) RNA export, but not protein import or export. These results demonstrate that two novel vertebrate nucleoporins, Nup160 and Nup133, not only interact with Nup98 and Nup153, but themselves play a role in mRNA export. The Rockefeller University Press 2001-10-29 /pmc/articles/PMC2150853/ /pubmed/11684705 http://dx.doi.org/10.1083/jcb.200108007 Text en Copyright © 2001, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Vasu, Sanjay
Shah, Sundeep
Orjalo, Arturo
Park, Minkyu
Fischer, Wolfgang H.
Forbes, Douglass J.
Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export
title Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export
title_full Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export
title_fullStr Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export
title_full_unstemmed Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export
title_short Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export
title_sort novel vertebrate nucleoporins nup133 and nup160 play a role in mrna export
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150853/
https://www.ncbi.nlm.nih.gov/pubmed/11684705
http://dx.doi.org/10.1083/jcb.200108007
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