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Quantitative Proteomics Identify Novel miR-155 Target Proteins

BACKGROUND: MicroRNAs are 22 nucleotides long non-coding RNAs and exert their function either by transcriptional or translational inhibition. Although many microRNA profiles in different tissues and disease states have already been discovered, only little is known about their target proteins. The mi...

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Autores principales: Lößner, Christopher, Meier, Jan, Warnken, Uwe, Rogers, Michael A., Lichter, Peter, Pscherer, Armin, Schnölzer, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143118/
https://www.ncbi.nlm.nih.gov/pubmed/21799781
http://dx.doi.org/10.1371/journal.pone.0022146
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author Lößner, Christopher
Meier, Jan
Warnken, Uwe
Rogers, Michael A.
Lichter, Peter
Pscherer, Armin
Schnölzer, Martina
author_facet Lößner, Christopher
Meier, Jan
Warnken, Uwe
Rogers, Michael A.
Lichter, Peter
Pscherer, Armin
Schnölzer, Martina
author_sort Lößner, Christopher
collection PubMed
description BACKGROUND: MicroRNAs are 22 nucleotides long non-coding RNAs and exert their function either by transcriptional or translational inhibition. Although many microRNA profiles in different tissues and disease states have already been discovered, only little is known about their target proteins. The microRNA miR-155 is deregulated in many diseases, including cancer, where it might function as an oncoMir. METHODOLOGY/PRINCIPAL FINDINGS: We employed a proteomics technique called “stable isotope labelling by amino acids in cell culture” (SILAC) allowing relative quantification to reliably identify target proteins of miR-155. Using SILAC, we identified 46 putative miR-155 target proteins, some of which were previously reported. With luciferase reporter assays, CKAP5 was confirmed as a new target of miR-155. Functional annotation of miR-155 target proteins pointed to a role in cell cycle regulation. CONCLUSIONS/SIGNIFICANCE: To the best of our knowledge we have investigated for the first time miR-155 target proteins in the HEK293T cell line in large scale. In addition, by comparing our results to previously identified miR-155 target proteins in other cell lines, we provided further evidence for the cell line specificity of microRNAs.
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spelling pubmed-31431182011-07-28 Quantitative Proteomics Identify Novel miR-155 Target Proteins Lößner, Christopher Meier, Jan Warnken, Uwe Rogers, Michael A. Lichter, Peter Pscherer, Armin Schnölzer, Martina PLoS One Research Article BACKGROUND: MicroRNAs are 22 nucleotides long non-coding RNAs and exert their function either by transcriptional or translational inhibition. Although many microRNA profiles in different tissues and disease states have already been discovered, only little is known about their target proteins. The microRNA miR-155 is deregulated in many diseases, including cancer, where it might function as an oncoMir. METHODOLOGY/PRINCIPAL FINDINGS: We employed a proteomics technique called “stable isotope labelling by amino acids in cell culture” (SILAC) allowing relative quantification to reliably identify target proteins of miR-155. Using SILAC, we identified 46 putative miR-155 target proteins, some of which were previously reported. With luciferase reporter assays, CKAP5 was confirmed as a new target of miR-155. Functional annotation of miR-155 target proteins pointed to a role in cell cycle regulation. CONCLUSIONS/SIGNIFICANCE: To the best of our knowledge we have investigated for the first time miR-155 target proteins in the HEK293T cell line in large scale. In addition, by comparing our results to previously identified miR-155 target proteins in other cell lines, we provided further evidence for the cell line specificity of microRNAs. Public Library of Science 2011-07-25 /pmc/articles/PMC3143118/ /pubmed/21799781 http://dx.doi.org/10.1371/journal.pone.0022146 Text en Lößner 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
Lößner, Christopher
Meier, Jan
Warnken, Uwe
Rogers, Michael A.
Lichter, Peter
Pscherer, Armin
Schnölzer, Martina
Quantitative Proteomics Identify Novel miR-155 Target Proteins
title Quantitative Proteomics Identify Novel miR-155 Target Proteins
title_full Quantitative Proteomics Identify Novel miR-155 Target Proteins
title_fullStr Quantitative Proteomics Identify Novel miR-155 Target Proteins
title_full_unstemmed Quantitative Proteomics Identify Novel miR-155 Target Proteins
title_short Quantitative Proteomics Identify Novel miR-155 Target Proteins
title_sort quantitative proteomics identify novel mir-155 target proteins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143118/
https://www.ncbi.nlm.nih.gov/pubmed/21799781
http://dx.doi.org/10.1371/journal.pone.0022146
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