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RNA Secondary Structure Prediction Using High-throughput SHAPE
Published on: May 31, 2013
Use of tiling array data and RNA secondary structure predictions to identify noncoding RNA genes
Christian Weile1, Paul P Gardner, Mads M Hedegaard
1Molecular Evolution Group, Department of Molecular Biology, University of Copenhagen, Copenhagen N, Denmark. cweile@yahoo.dk <cweile@yahoo.dk>
BMC Genomics
|July 25, 2007
Summary
Thousands of novel human noncoding RNA genes, including structured and conserved types, are discoverable. Combining genome-wide transcription data with RNA structure predictions enhances the identification of these crucial genetic elements.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Recent discoveries highlight a vast number of noncoding RNA genes, suggesting many more await identification.
- Comparative genomics reveals numerous human DNA sequences with conserved RNA secondary structures.
- Genome-wide transcription profiling indicates extensive transcriptional activity across the human genome.
Purpose of the Study:
- To identify novel noncoding and structural RNA genes expressed in human cells.
- To leverage comparative genomics and tiling array data for enhanced RNA gene discovery.
Main Methods:
- Combined tiling array data with genome-wide structural RNA predictions.
- Focused on candidate genes with stable hairpin structures or high covariance for verification.
- Utilized northern blotting to confirm gene expression.
Main Results:
- Identified thousands of candidate human RNA genes using the combined strategy.
- Verified the expression of 2 out of 3 hairpin structures and 3 out of 9 high covariance structures in SK-N-AS cells.
- Demonstrated the efficacy of the integrated approach in discovering expressed RNA genes.
Conclusions:
- Numerous human noncoding, structured, and conserved RNA genes remain undiscovered.
- Tissue-specific tiling array data combined with computational predictions improve the search for structural RNA genes.
- This integrated approach offers a powerful strategy for uncovering novel RNA gene functions.
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