TY - JOUR
T1 - Context-specific microRNA analysis
T2 - Identification of functional microRNAs and their mRNA targets
AU - Ben-Moshe, Noa Bossel
AU - Avraham, Roi
AU - Kedmi, Merav
AU - Zeisel, Amit
AU - Yitzhaky, Assif
AU - Yarden, Yosef
AU - Domany, Eytan
N1 - The Leir Charitable Foundation; Israel Science Foundation (ISF); MD Moross Institute for Cancer Research; Dr Miriam and Sheldon Adelson Medical Research Foundation; German Research Foundation (DIP); National Cancer Institute [CA72981]Funding for open access charge: The Leir Charitable Foundation; the Israel Science Foundation (ISF); the MD Moross Institute for Cancer Research; the Dr Miriam and Sheldon Adelson Medical Research Foundation; the German Research Foundation (DIP) and the National Cancer Institute [CA72981].
PY - 2012/11
Y1 - 2012/11
N2 - MicroRNAs (miRs) function primarily as post-transcriptional negative regulators of gene expression through binding to their mRNA targets. Reliable prediction of a miR's targets is a considerable bioinformatic challenge of great importance for inferring the miR's function. Sequence-based prediction algorithms have high false-positive rates, are not in agreement, and are not biological context specific. Here we introduce CoSMic (Context-Specific MicroRNA analysis), an algorithm that combines sequence-based prediction with miR and mRNA expression data. CoSMic differs from existing methods-it identifies miRs that play active roles in the specific biological system of interest and predicts with less false positives their functional targets. We applied CoSMic to search for miRs that regulate the migratory response of human mammary cells to epidermal growth factor (EGF) stimulation. Several such miRs, whose putative targets were significantly enriched by migration processes were identified. We tested three of these miRs experimentally, and showed that they indeed affected the migratory phenotype; we also tested three negative controls. In comparison to other algorithms CoSMic indeed filters out false positives and allows improved identification of context-specific targets. CoSMic can greatly facilitate miR research in general and, in particular, advance our understanding of individual miRs' function in a specific context.
AB - MicroRNAs (miRs) function primarily as post-transcriptional negative regulators of gene expression through binding to their mRNA targets. Reliable prediction of a miR's targets is a considerable bioinformatic challenge of great importance for inferring the miR's function. Sequence-based prediction algorithms have high false-positive rates, are not in agreement, and are not biological context specific. Here we introduce CoSMic (Context-Specific MicroRNA analysis), an algorithm that combines sequence-based prediction with miR and mRNA expression data. CoSMic differs from existing methods-it identifies miRs that play active roles in the specific biological system of interest and predicts with less false positives their functional targets. We applied CoSMic to search for miRs that regulate the migratory response of human mammary cells to epidermal growth factor (EGF) stimulation. Several such miRs, whose putative targets were significantly enriched by migration processes were identified. We tested three of these miRs experimentally, and showed that they indeed affected the migratory phenotype; we also tested three negative controls. In comparison to other algorithms CoSMic indeed filters out false positives and allows improved identification of context-specific targets. CoSMic can greatly facilitate miR research in general and, in particular, advance our understanding of individual miRs' function in a specific context.
UR - http://www.scopus.com/inward/record.url?scp=84870612323&partnerID=8YFLogxK
U2 - https://doi.org/10.1093/nar/gks841
DO - https://doi.org/10.1093/nar/gks841
M3 - مقالة
SN - 0305-1048
VL - 40
SP - 10614
EP - 10627
JO - Nucleic acids research
JF - Nucleic acids research
IS - 21
ER -