Book contents
- Frontmatter
- Contents
- List of contributors
- Foreword by Sidney Altman
- Foreword by Victor R. Ambros
- Introduction
- I Discovery of microRNAs in various organisms
- II MicroRNA functions and RNAi-mediated pathways
- III Computational biology of microRNAs
- 11 miRBase: a database of microRNA sequences, targets and nomenclature
- 12 Computational prediction of microRNA targets in vertebrates, fruitflies and nematodes
- 13 Computational approaches to elucidate miRNA biology
- 14 The RNAhybrid approach to microRNA target prediction
- 15 Machine learning predicts microRNA target sites
- 16 Models of microRNA–target coordination
- IV Detection and quantitation of microRNAs
- V MicroRNAs in disease biology
- VI MicroRNAs in stem cell development
- Index
- Plate section
- References
13 - Computational approaches to elucidate miRNA biology
from III - Computational biology of microRNAs
Published online by Cambridge University Press: 22 August 2009
- Frontmatter
- Contents
- List of contributors
- Foreword by Sidney Altman
- Foreword by Victor R. Ambros
- Introduction
- I Discovery of microRNAs in various organisms
- II MicroRNA functions and RNAi-mediated pathways
- III Computational biology of microRNAs
- 11 miRBase: a database of microRNA sequences, targets and nomenclature
- 12 Computational prediction of microRNA targets in vertebrates, fruitflies and nematodes
- 13 Computational approaches to elucidate miRNA biology
- 14 The RNAhybrid approach to microRNA target prediction
- 15 Machine learning predicts microRNA target sites
- 16 Models of microRNA–target coordination
- IV Detection and quantitation of microRNAs
- V MicroRNAs in disease biology
- VI MicroRNAs in stem cell development
- Index
- Plate section
- References
Summary
Introduction
Research in the past decade has revealed that microRNAs (miRNAs) are widespread and that they are likely to underlie an appreciably larger set of disease processes than is currently known. The first miRNAs and their functions were determined via classical genetic techniques. Soon after, a number of miRNAs were discovered experimentally (Lagos-Quintana et al., 2001). However, the characterization of miRNA function remained elusive owing to low-throughput experiments and often indeterminate results, most notably for those miRNAs which have multiple roles in multiple tissues. High-throughput experimental methods for miRNA target identification are the ideal solution, but such methods are not currently available. As a result, computational methods were developed, and are still regularly used, for the purpose of identifying miRNA targets.
Most current target prediction programs require the sequences of known miRNAs. Currently, there are 332 known miRNAs in the human genome. The estimation of the total number of miRNAs varies from publication to publication (Lim et al., 2003; Bentwich et al., 2005). In a recent paper, Bentwich et al. contended that there are at least 500 more miRNAs that are yet to be identified (Bentwich et al., 2005). Despite the number of unknown miRNAs, computational approaches based on features of known miRNAs have been instrumental in the discovery of as-of-yet-unknown miRNAs in the genome. The past few years have witnessed an explosion in information regarding the genomic organization of miRNAs, the biogenesis of miRNAs, the targeting mechanisms of miRNAs, and the regulatory networks in which miRNAs are involved.
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- Information
- MicroRNAsFrom Basic Science to Disease Biology, pp. 187 - 198Publisher: Cambridge University PressPrint publication year: 2007