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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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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. |
format | Online Article Text |
id | pubmed-3143118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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