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Luzp4 defines a new mRNA export pathway in cancer cells
Cancer testis antigens (CTAs) represented a poorly characterized group of proteins whose expression is normally restricted to testis but are frequently up-regulated in cancer cells. Here we show that one CTA, Luzp4, is an mRNA export adaptor. It associates with the TREX mRNA export complex subunit U...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344508/ https://www.ncbi.nlm.nih.gov/pubmed/25662211 http://dx.doi.org/10.1093/nar/gkv070 |
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author | Viphakone, Nicolas Cumberbatch, Marcus G. Livingstone, Michaela J. Heath, Paul R. Dickman, Mark J. Catto, James W. Wilson, Stuart A. |
author_facet | Viphakone, Nicolas Cumberbatch, Marcus G. Livingstone, Michaela J. Heath, Paul R. Dickman, Mark J. Catto, James W. Wilson, Stuart A. |
author_sort | Viphakone, Nicolas |
collection | PubMed |
description | Cancer testis antigens (CTAs) represented a poorly characterized group of proteins whose expression is normally restricted to testis but are frequently up-regulated in cancer cells. Here we show that one CTA, Luzp4, is an mRNA export adaptor. It associates with the TREX mRNA export complex subunit Uap56 and harbours a Uap56 binding motif, conserved in other mRNA export adaptors. Luzp4 binds the principal mRNA export receptor Nxf1, enhances its RNA binding activity and complements Alyref knockdown in vivo. Whilst Luzp4 is up-regulated in a range of tumours, it appears preferentially expressed in melanoma cells where it is required for growth. |
format | Online Article Text |
id | pubmed-4344508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43445082015-03-17 Luzp4 defines a new mRNA export pathway in cancer cells Viphakone, Nicolas Cumberbatch, Marcus G. Livingstone, Michaela J. Heath, Paul R. Dickman, Mark J. Catto, James W. Wilson, Stuart A. Nucleic Acids Res RNA Cancer testis antigens (CTAs) represented a poorly characterized group of proteins whose expression is normally restricted to testis but are frequently up-regulated in cancer cells. Here we show that one CTA, Luzp4, is an mRNA export adaptor. It associates with the TREX mRNA export complex subunit Uap56 and harbours a Uap56 binding motif, conserved in other mRNA export adaptors. Luzp4 binds the principal mRNA export receptor Nxf1, enhances its RNA binding activity and complements Alyref knockdown in vivo. Whilst Luzp4 is up-regulated in a range of tumours, it appears preferentially expressed in melanoma cells where it is required for growth. Oxford University Press 2015-02-27 2015-02-06 /pmc/articles/PMC4344508/ /pubmed/25662211 http://dx.doi.org/10.1093/nar/gkv070 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA Viphakone, Nicolas Cumberbatch, Marcus G. Livingstone, Michaela J. Heath, Paul R. Dickman, Mark J. Catto, James W. Wilson, Stuart A. Luzp4 defines a new mRNA export pathway in cancer cells |
title | Luzp4 defines a new mRNA export pathway in cancer cells |
title_full | Luzp4 defines a new mRNA export pathway in cancer cells |
title_fullStr | Luzp4 defines a new mRNA export pathway in cancer cells |
title_full_unstemmed | Luzp4 defines a new mRNA export pathway in cancer cells |
title_short | Luzp4 defines a new mRNA export pathway in cancer cells |
title_sort | luzp4 defines a new mrna export pathway in cancer cells |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344508/ https://www.ncbi.nlm.nih.gov/pubmed/25662211 http://dx.doi.org/10.1093/nar/gkv070 |
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