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Distinct MicroRNA Subcellular Size and Expression Patterns in Human Cancer Cells

Introduction. Small noncoding RNAs have important regulatory functions in different cell pathways. It is believed that most of them mainly play role in gene post-transcriptional regulation in the cytoplasm. Recent evidence suggests miRNA and siRNA activity in the nucleus. Here, we show distinct geno...

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Autores principales: Chen, Beibei, Zhang, Bo, Luo, Huaxia, Yuan, Jiao, Skogerbø, Geir, Chen, Runsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296955/
https://www.ncbi.nlm.nih.gov/pubmed/22505932
http://dx.doi.org/10.1155/2012/672462
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author Chen, Beibei
Zhang, Bo
Luo, Huaxia
Yuan, Jiao
Skogerbø, Geir
Chen, Runsheng
author_facet Chen, Beibei
Zhang, Bo
Luo, Huaxia
Yuan, Jiao
Skogerbø, Geir
Chen, Runsheng
author_sort Chen, Beibei
collection PubMed
description Introduction. Small noncoding RNAs have important regulatory functions in different cell pathways. It is believed that most of them mainly play role in gene post-transcriptional regulation in the cytoplasm. Recent evidence suggests miRNA and siRNA activity in the nucleus. Here, we show distinct genome-wide sub-cellular localization distribution profiles of small noncoding RNAs in human breast cancer cells. Methods. We separated breast cancer cell nuclei from cytoplasm, and identified small RNA sequences using a high-throughput sequencing platform. To determine the relationship between miRNA sub-cellular distribution and cancer progression, we used microarray analysis to examine the miRNA expression levels in nucleus and cytoplasm of three human cell lines, one normal breast cell line and two breast cancer cell lines. Logistic regression and SVM were used for further analysis. Results. The sub-cellular distribution of small noncoding RNAs shows that numerous miRNAs and their isoforms (isomiR) not only locate to the cytoplasm but also appeare in the nucleus. Subsequent microarray analyses indicated that the miRNA nuclear-cytoplasmic-ratio is a significant characteristic of different cancer cell lines. Conclusions. Our results indicate that the sub-cellular distribution is important for miRNA function, and that the characterization of the small RNAs sub-cellular localizome may contribute to cancer research and diagnosis.
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spelling pubmed-32969552012-04-13 Distinct MicroRNA Subcellular Size and Expression Patterns in Human Cancer Cells Chen, Beibei Zhang, Bo Luo, Huaxia Yuan, Jiao Skogerbø, Geir Chen, Runsheng Int J Cell Biol Research Article Introduction. Small noncoding RNAs have important regulatory functions in different cell pathways. It is believed that most of them mainly play role in gene post-transcriptional regulation in the cytoplasm. Recent evidence suggests miRNA and siRNA activity in the nucleus. Here, we show distinct genome-wide sub-cellular localization distribution profiles of small noncoding RNAs in human breast cancer cells. Methods. We separated breast cancer cell nuclei from cytoplasm, and identified small RNA sequences using a high-throughput sequencing platform. To determine the relationship between miRNA sub-cellular distribution and cancer progression, we used microarray analysis to examine the miRNA expression levels in nucleus and cytoplasm of three human cell lines, one normal breast cell line and two breast cancer cell lines. Logistic regression and SVM were used for further analysis. Results. The sub-cellular distribution of small noncoding RNAs shows that numerous miRNAs and their isoforms (isomiR) not only locate to the cytoplasm but also appeare in the nucleus. Subsequent microarray analyses indicated that the miRNA nuclear-cytoplasmic-ratio is a significant characteristic of different cancer cell lines. Conclusions. Our results indicate that the sub-cellular distribution is important for miRNA function, and that the characterization of the small RNAs sub-cellular localizome may contribute to cancer research and diagnosis. Hindawi Publishing Corporation 2012 2012-02-12 /pmc/articles/PMC3296955/ /pubmed/22505932 http://dx.doi.org/10.1155/2012/672462 Text en Copyright © 2012 Beibei Chen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Beibei
Zhang, Bo
Luo, Huaxia
Yuan, Jiao
Skogerbø, Geir
Chen, Runsheng
Distinct MicroRNA Subcellular Size and Expression Patterns in Human Cancer Cells
title Distinct MicroRNA Subcellular Size and Expression Patterns in Human Cancer Cells
title_full Distinct MicroRNA Subcellular Size and Expression Patterns in Human Cancer Cells
title_fullStr Distinct MicroRNA Subcellular Size and Expression Patterns in Human Cancer Cells
title_full_unstemmed Distinct MicroRNA Subcellular Size and Expression Patterns in Human Cancer Cells
title_short Distinct MicroRNA Subcellular Size and Expression Patterns in Human Cancer Cells
title_sort distinct microrna subcellular size and expression patterns in human cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296955/
https://www.ncbi.nlm.nih.gov/pubmed/22505932
http://dx.doi.org/10.1155/2012/672462
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