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miRNA Biogenesis

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Cover of 'miRNA Biogenesis'

Table of Contents

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    Book Overview
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    Chapter 1 High-Throughput Characterization of Primary microRNA Transcripts
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    Chapter 2 Identifying Pri-miRNA Transcription Start Sites
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    Chapter 3 Metabolic Pulse-Chase RNA Labeling for pri-miRNA Processing Dynamics
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    Chapter 4 In Vitro System for Coupling RNAP II Transcription to Primary microRNA Processing and a Three-Way System for RNAP II Transcription/Splicing/microRNA Processing
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    Chapter 5 Purification of Microprocessor-Associated Factors
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    Chapter 6 Inhibiting Pri-miRNA Processing with Target Site Blockers
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    Chapter 7 MicroRNA Analysis Using the Quantitative Real-Time PCR Reaction
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    Chapter 8 MicroRNA Analysis Using Next-Generation Sequencing
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    Chapter 9 Identification of microRNA Precursor-Associated Proteins
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    Chapter 10 Analysis of 3′ End Modifications in microRNAs by High-Throughput Sequencing
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    Chapter 11 Uncovering the Stability of Mature miRNAs by 4-Thio-Uridine Metabolic Labeling
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    Chapter 12 Detection of microRNA-Target Interactions by Chimera PCR (ChimP)
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    Chapter 13 High-Quality Overlapping Paired-End Reads for the Detection of A-to-I Editing on Small RNA
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    Chapter 14 Targeting miRNA for Therapeutics Using a Micronome Based Method for Identification of miRNA-mRNA Pairs and Validation of Key Regulator miRNA
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    Chapter 15 Method for Detection of miRNAs in Non-Model Organisms with Unreported Database
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    Chapter 16 Detection and Verification of Mammalian Mirtrons by Northern Blotting
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    Chapter 17 Detecting Agotrons in Ago CLIPseq Data
Attention for Chapter 17: Detecting Agotrons in Ago CLIPseq Data
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Chapter title
Detecting Agotrons in Ago CLIPseq Data
Chapter number 17
Book title
miRNA Biogenesis
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-8624-8_17
Pubmed ID
Book ISBNs
978-1-4939-8623-1, 978-1-4939-8624-8
Authors

Thomas B. Hansen, Hansen, Thomas B.

Abstract

Timely and accurate regulation of gene expression is essential to all organisms. MicroRNAs (miRNAs) are a well-characterized and important class of gene expression regulators. We recently identified a novel class of gene regulators, the agotrons. Agotrons derive from short introns and associate with Argonaute (Ago) proteins much similar to miRNAs. However, agotrons completely bypass the conventional miRNA biogenesis pathway and thus exist as full-length introns, which disobey the classical rules on Ago-substrate requirements. As a class, agotrons are conserved in mammals, and despite the non-canonical biogenesis pathway, agotrons maintain the ability to deregulate mRNAs with seed-matches in the 3'UTR. While several pipelines exist for the detection of miRNAs, no bioinformatics toolkit has yet been developed to specifically identify agotrons. Here, we describe a simple approach, termed agotron_detector ( https://github.com/ncrnalab/agotron_detector ), to identify and quantify agotrons in Ago CLIPseq datasets. Hopefully, this allows researchers worldwide to characterize agotrons in more detail and to reveal the biological relevance of these fascinating RNA species.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 4 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 25%
Professor > Associate Professor 1 25%
Unknown 2 50%
Readers by discipline Count As %
Agricultural and Biological Sciences 2 50%
Unknown 2 50%