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This article is part of the supplement: Proceedings of the 2011 International Conference on Bioinformatics and Computational Biology (BIOCOMP'11)

Open Access Highly Accessed Research

Potential roles of microRNAs in regulating long intergenic noncoding RNAs

Liran Juan15, Guohua Wang1, Milan Radovich2, Bryan P Schneider3, Susan E Clare2, Yadong Wang1* and Yunlong Liu45*

Author Affiliations

1 Center for Biomedical Informatics, Harbin Institute of Technology School of Computer Science and Technology, Harbin, Heilongjiang 150001, China

2 Department of Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA

3 Department of Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA

4 Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, USA

5 Center for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, IN 46202, USA

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BMC Medical Genomics 2013, 6(Suppl 1):S7  doi:10.1186/1755-8794-6-S1-S7

Published: 23 January 2013

Abstract

Background

Over 10,000 long intergenic non-coding RNAs (lincRNAs) have been identified in the human genome. Some have been well characterized and known to participate in various stages of gene regulation. In the post-transcriptional process, another class of well-known small non-coding RNA, or microRNA (miRNA), is very active in inhibiting mRNA. Though similar features between mRNA and lincRNA have been revealed in several recent studies, and a few isolated miRNA-lincRNA relationships have been observed. Despite these advances, the comprehensive miRNA regulation pattern of lincRNA has not been clarified.

Methods

In this study, we investigated the possible interaction between the two classes of non-coding RNAs. Instead of using the existing long non-coding database, we employed an ab initio method to annotate lincRNAs expressed in a group of normal breast tissues and breast tumors.

Results

Approximately 90 lincRNAs show strong reverse expression correlation with miRNAs, which have at least one predicted target site presented. These target sites are statistically more conserved than their neighboring genetic regions and other predicted target sites. Several miRNAs that target to these lincRNAs are known to play an essential role in breast cancer.

Conclusion

Similar to inhibiting mRNAs, miRNAs show potential in promoting the degeneration of lincRNAs. Breast-cancer-related miRNAs may influence their target lincRNAs resulting in differential expression in normal and malignant breast tissues. This implies the miRNA regulation of lincRNAs may be involved in the regulatory process in tumor cells.