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Identification of microRNAs with regulatory potential using a matched microRNA-mRNA time-course data
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Lutherborrow, Mark
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Univ New S Wales, St Vincents Hosp, Dept Haematol, St Vincent Ctr Appl Biomed Res,Blood Stem Cell &, Darlinghurst, NSW, Australia
Univ New S Wales, St Vincents Clin Sch, Darlinghurst, NSW, Australia Univ Sydney, Sch Math & Stat, Sydney, NSW 2006, Australia

Ma, David D. F.
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Univ New S Wales, St Vincents Hosp, Dept Haematol, St Vincent Ctr Appl Biomed Res,Blood Stem Cell &, Darlinghurst, NSW, Australia
Univ New S Wales, St Vincents Clin Sch, Darlinghurst, NSW, Australia Univ Sydney, Sch Math & Stat, Sydney, NSW 2006, Australia

Yang, Yee Hwa
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Univ Sydney, Sch Math & Stat, Sydney, NSW 2006, Australia
Univ Sydney, Ctr Math Biol, Sydney, NSW 2006, Australia Univ Sydney, Sch Math & Stat, Sydney, NSW 2006, Australia
机构:
[1] Univ Sydney, Sch Math & Stat, Sydney, NSW 2006, Australia
[2] Univ Sydney, Ctr Math Biol, Sydney, NSW 2006, Australia
[3] Univ New S Wales, St Vincents Hosp, Dept Haematol, St Vincent Ctr Appl Biomed Res,Blood Stem Cell &, Darlinghurst, NSW, Australia
[4] Univ New S Wales, St Vincents Clin Sch, Darlinghurst, NSW, Australia
基金:
澳大利亚研究理事会;
关键词:
EXPRESSION;
GENES;
NORMALIZATION;
DISCOVERY;
TARGETS;
PROTEIN;
DNMT3B;
D O I:
10.1093/nar/gkp153
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Over the past decade, a class of small RNA molecules called microRNAs (miRNAs) has been shown to regulate gene expression at the post-transcription stage. While early work focused on the identification of miRNAs using a combination of experimental and computational techniques, subsequent studies have focused on identification of miRNA-target mRNA pairs as each miRNA can have hundreds of mRNA targets. The experimental validation of some miRNAs as oncogenic has provided further motivation for research in this area. In this article we propose an odds-ratio (OR) statistic for identification of regulatory miRNAs. It is based on integrative analysis of matched miRNA and mRNA time-course microarray data. The OR-statistic was used for (i) identification of miRNAs with regulatory potential, (ii) identification of miRNA-target mRNA pairs and (iii) identification of time lags between changes in miRNA expression and those of its target mRNAs. We applied the OR-statistic to a cancer data set and identified a small set of miRNAs that were negatively correlated to mRNAs. A literature survey revealed that some of the miRNAs that were predicted to be regulatory, were indeed oncogenic or tumor suppressors. Finally, some of the predicted miRNA targets have been shown to be experimentally valid.
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