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PMID: 20975837 Published · epublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Exprtarget: an integrative approach to predicting human microRNA targets.

PloS one ·Vol. 5 ·No. 10 ·2010-10-21 ·Pages e13534

Gamazon ER, Im HK, Duan S, Lussier YA, Cox NJ, Dolan ME, Zhang W

Abstract

Variation in gene expression has been observed in natural populations and associated with complex traits or phenotypes such as disease susceptibility and drug response. Gene expression itself is controlled by various genetic and non-genetic factors. The binding of a class of small RNA molecules, microRNAs (miRNAs), to mRNA transcript targets has recently been demonstrated to be an important mechanism of gene regulation. Because individual miRNAs may regulate the expression of multiple gene targets, a comprehensive and reliable catalogue of miRNA-regulated targets is critical to understanding gene regulatory networks. Though experimental approaches have been used to identify many miRNA targets, due to cost and efficiency, current miRNA target identification still relies largely on computational algorithms that aim to take advantage of different biochemical/thermodynamic properties of the sequences of miRNAs and their gene targets. A novel approach, ExprTarget, therefore, is proposed here to integrate some of the most frequently invoked methods (miRanda, PicTar, TargetScan) as well as the genome-wide HapMap miRNA and mRNA expression datasets generated in our laboratory. To our knowledge, this dataset constitutes the first miRNA expression profiling in the HapMap lymphoblastoid cell lines. We conducted diagnostic tests of the existing computational solutions using the experimentally supported targets in TarBase as gold standard. To gain insight into the biases that arise from such an analysis, we investigated the effect of the choice of gold standard on the evaluation of the various computational tools. We analyzed the performance of ExprTarget using both ROC curve analysis and cross-validation. We show that ExprTarget greatly improves miRNA target prediction relative to the individual prediction algorithms in terms of sensitivity and specificity. We also developed an online database, ExprTargetDB, of human miRNA targets predicted by our approach that integrates gene expression profiling into a broader framework involving important features of miRNA target site predictions.

MeSH Terms
Algorithms Humans MicroRNAs/genetics Thermodynamics
Chemicals
MicroRNAs
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Gamazon Eric R
Department of Medicine, University of Chicago, Chicago, Illinois, United States of America.
Im Hae-Kyung
Duan Shiwei
Lussier Yves A
Cox Nancy J
Dolan M Eileen
Zhang Wei
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Article Info
Journal
PloS one
Abbr.
PLoS One
ISSN
1932-6203
Published
2010-10-21
Epub
2010-00-21
Pages
e13534
Language
English
Region
United States
NLM ID
101285081
PMCID
PMC2958831
Subset
IM
Grants
NIGMS NIH HHS · U01 GM061393 · United States
NCI NIH HHS · P50 CA125183 · United States
NIGMS NIH HHS · U01GM61393 · United States
NCI NIH HHS · CA139278 · United States
NIGMS NIH HHS · U01GM61374 · United States
NCI NIH HHS · R21 CA139278 · United States
NCI NIH HHS · U54 CA121852 · United States
NIGMS NIH HHS · U01 GM061374 · United States
NLM NIH HHS · K22 LM008308 · United States
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