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ZFAS1: a long noncoding RNA associated with ribosomes in breast cancer cells

BACKGROUND: Most of the eukaryotic genome is transcribed, yielding a complex network of transcripts including thousands of lncRNAs that generally lack protein coding potential. However, only a small percentage of these molecules has been functionally characterised, and discoveries of specific functi...

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Autores principales: Hansji, Herah, Leung, Euphemia Y., Baguley, Bruce C., Finlay, Graeme J., Cameron-Smith, David, Figueiredo, Vandre C., Askarian-Amiri, Marjan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117590/
https://www.ncbi.nlm.nih.gov/pubmed/27871336
http://dx.doi.org/10.1186/s13062-016-0165-y
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author Hansji, Herah
Leung, Euphemia Y.
Baguley, Bruce C.
Finlay, Graeme J.
Cameron-Smith, David
Figueiredo, Vandre C.
Askarian-Amiri, Marjan E.
author_facet Hansji, Herah
Leung, Euphemia Y.
Baguley, Bruce C.
Finlay, Graeme J.
Cameron-Smith, David
Figueiredo, Vandre C.
Askarian-Amiri, Marjan E.
author_sort Hansji, Herah
collection PubMed
description BACKGROUND: Most of the eukaryotic genome is transcribed, yielding a complex network of transcripts including thousands of lncRNAs that generally lack protein coding potential. However, only a small percentage of these molecules has been functionally characterised, and discoveries of specific functions demonstrate layers of complexity. A large percentage of lncRNAs is located in the cytoplasm, associated with ribosomes but the function of the majority of these transcripts is unclear. The current study analyses putative mechanisms of action of the lncRNA species member ZFAS1 that was initially discovered by microarray analysis of murine tissues undergoing mammary gland development. As developmental genes are often deregulated in cancer, here we have studied its function in breast cancer cell lines. RESULTS: Using human breast cancer cell lines, ZFAS1 was found to be expressed in all cell lines tested, albeit at different levels of abundance. Following subcellular fractionation, human ZFAS1 was found in both nucleus and cytoplasm (as is the mouse orthologue) in an isoform-independent manner. Sucrose gradients based on velocity sedimentation were utilised to separate the different components of total cell lysate, and surprisingly ZFAS1 was primarily co-localised with light polysomes. Further investigation into ribosome association through subunit dissociation studies showed that ZFAS1 was predominantly associated with the 40S small ribosomal subunit. The expression levels of ZFAS1 and of mRNAs encoding several ribosomal proteins that have roles in ribosome assembly, production and maturation were tightly correlated. ZFAS1 knockdown significantly reduced RPS6 phosphorylation. CONCLUSION: A large number of lncRNAs associate with ribosomes but the function of the majority of these lncRNAs has not been elucidated. The association of the lncRNA ZFAS1 with a subpopulation of ribosomes and the correlation with expression of mRNAs for ribosomal proteins suggest a ribosome-interacting mechanism pertaining to their assembly or biosynthetic activity. ZFAS1 may represent a new class of lncRNAs which associates with ribosomes to regulate their function. REVIEWERS: This article was reviewed by Christine Vande Velde, Nicola Aceto and Haruhiko Siomi. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13062-016-0165-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-51175902016-11-28 ZFAS1: a long noncoding RNA associated with ribosomes in breast cancer cells Hansji, Herah Leung, Euphemia Y. Baguley, Bruce C. Finlay, Graeme J. Cameron-Smith, David Figueiredo, Vandre C. Askarian-Amiri, Marjan E. Biol Direct Research BACKGROUND: Most of the eukaryotic genome is transcribed, yielding a complex network of transcripts including thousands of lncRNAs that generally lack protein coding potential. However, only a small percentage of these molecules has been functionally characterised, and discoveries of specific functions demonstrate layers of complexity. A large percentage of lncRNAs is located in the cytoplasm, associated with ribosomes but the function of the majority of these transcripts is unclear. The current study analyses putative mechanisms of action of the lncRNA species member ZFAS1 that was initially discovered by microarray analysis of murine tissues undergoing mammary gland development. As developmental genes are often deregulated in cancer, here we have studied its function in breast cancer cell lines. RESULTS: Using human breast cancer cell lines, ZFAS1 was found to be expressed in all cell lines tested, albeit at different levels of abundance. Following subcellular fractionation, human ZFAS1 was found in both nucleus and cytoplasm (as is the mouse orthologue) in an isoform-independent manner. Sucrose gradients based on velocity sedimentation were utilised to separate the different components of total cell lysate, and surprisingly ZFAS1 was primarily co-localised with light polysomes. Further investigation into ribosome association through subunit dissociation studies showed that ZFAS1 was predominantly associated with the 40S small ribosomal subunit. The expression levels of ZFAS1 and of mRNAs encoding several ribosomal proteins that have roles in ribosome assembly, production and maturation were tightly correlated. ZFAS1 knockdown significantly reduced RPS6 phosphorylation. CONCLUSION: A large number of lncRNAs associate with ribosomes but the function of the majority of these lncRNAs has not been elucidated. The association of the lncRNA ZFAS1 with a subpopulation of ribosomes and the correlation with expression of mRNAs for ribosomal proteins suggest a ribosome-interacting mechanism pertaining to their assembly or biosynthetic activity. ZFAS1 may represent a new class of lncRNAs which associates with ribosomes to regulate their function. REVIEWERS: This article was reviewed by Christine Vande Velde, Nicola Aceto and Haruhiko Siomi. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13062-016-0165-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-21 /pmc/articles/PMC5117590/ /pubmed/27871336 http://dx.doi.org/10.1186/s13062-016-0165-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Hansji, Herah
Leung, Euphemia Y.
Baguley, Bruce C.
Finlay, Graeme J.
Cameron-Smith, David
Figueiredo, Vandre C.
Askarian-Amiri, Marjan E.
ZFAS1: a long noncoding RNA associated with ribosomes in breast cancer cells
title ZFAS1: a long noncoding RNA associated with ribosomes in breast cancer cells
title_full ZFAS1: a long noncoding RNA associated with ribosomes in breast cancer cells
title_fullStr ZFAS1: a long noncoding RNA associated with ribosomes in breast cancer cells
title_full_unstemmed ZFAS1: a long noncoding RNA associated with ribosomes in breast cancer cells
title_short ZFAS1: a long noncoding RNA associated with ribosomes in breast cancer cells
title_sort zfas1: a long noncoding rna associated with ribosomes in breast cancer cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117590/
https://www.ncbi.nlm.nih.gov/pubmed/27871336
http://dx.doi.org/10.1186/s13062-016-0165-y
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