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The sufficient minimal set of miRNA seed types

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TLDR
This work identified a set of canonical seed types based on a transcriptome wide analysis of experimentally verified functional target sites and confirmed the specificity of long seeds but found that the majority offunctional target sites are formed by less specific seeds of only 6 nt indicating a crucial role of this type.
Abstract
Motivation: Pairing between the target sequence and the 6–8 nt long seed sequence of the miRNA presents the most important feature for miRNA target site prediction. Novel high-throughput technologies such as Argonaute HITS-CLIP afford meanwhile a detailed study of miRNA:mRNA duplices. These interaction maps enable a first discrimination between functional and non-functional target sites in a bulky fashion. Prediction algorithms apply different seed paradigms to identify miRNA target sites. Therefore, a quantitative assessment of miRNA target site prediction is of major interest. Results: We identified a set of canonical seed types based on a transcriptome wide analysis of experimentally verified functional target sites. We confirmed the specificity of long seeds but we found that the majority of functional target sites are formed by less specific seeds of only 6 nt indicating a crucial role of this type. A substantial fraction of genuine target sites arenon-conserved. Moreover, the majority of functional sites remain uncovered by common prediction methods. Contact: florian.buettner@helmholtz-muenchen.de v.stuempflen@helmholtz-muenchen.de Supplementary Information: Supplementary data are available at Bioinformatics online.

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Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation.

TL;DR: An update on canonical and non-canonical miRNA biogenesis pathways and various mechanisms underlying miRNA-mediated gene regulations and the current knowledge of the dynamics of miRNA action and of the secretion, transfer, and uptake of extracellular miRNAs is provided.

MicroRNAs: Target Recognition and Regulatory Functions

TL;DR: In this article, a review outlines the current understanding of miRNA target recognition in animals and discusses the widespread impact of miRNAs on both the expression and evolution of protein-coding genes.
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Endogenous RNAs Modulate MicroRNA Sorting to Exosomes and Transfer to Acceptor Cells

TL;DR: RNA profiling of macrophages and their exosomes shows that miRNA sorting to exosome is modulated by cell-activation-dependent changes of miRNA target levels in the producer cells, and the use of Dicer-deficient cells and reporter lentiviral vectors for miRNA activity shows that exosomal miRNAs are transferred from macrophage to ECs to detectably repress targeted sequences.
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Identifying miRNAs, targets and functions

TL;DR: This review focuses on computational methods of inferring miRNA functions, including miRNA functional annotation and inferringMiRNAs regulatory modules, by integrating heterogeneous data sources and briefly introduces the research in miRNA discovery and miRNA-target identification.
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miRmap: Comprehensive prediction of microRNA target repression strength

TL;DR: An open-source software library, miRmap, which for the first time comprehensively covers all four approaches using 11 predictor features, 3 of which are novel, and concludes that target site accessibility appears to be the most predictive feature.
References
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Journal ArticleDOI

MicroRNAs: Target Recognition and Regulatory Functions

TL;DR: The current understanding of miRNA target recognition in animals is outlined and the widespread impact of miRNAs on both the expression and evolution of protein-coding genes is discussed.
Journal ArticleDOI

Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets

TL;DR: In a four-genome analysis of 3' UTRs, approximately 13,000 regulatory relationships were detected above the estimate of false-positive predictions, thereby implicating as miRNA targets more than 5300 human genes, which represented 30% of the gene set.
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Most mammalian mRNAs are conserved targets of microRNAs

TL;DR: This work overhauled its tool for finding preferential conservation of sequence motifs and applied it to the analysis of human 3'UTRs, increasing by nearly threefold the detected number of preferentially conserved miRNA target sites.
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Prediction of Mammalian MicroRNA Targets

TL;DR: The predicted regulatory targets of mammalian miRNAs were enriched for genes involved in transcriptional regulation but also encompassed an unexpectedly broad range of other functions.
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Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs

TL;DR: These results suggest that metazoan miRNAs can reduce the levels of many of their target transcripts, not just the amount of protein deriving from these transcripts, and seem to downregulate a far greater number of targets than previously appreciated.
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