Lamandé mRNA Decay

Methods and Protocols
1. Auflage 2018
ISBN: 978-1-4939-7540-2
Verlag: Springer US
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, Band 1720, 227 Seiten, eBook

Reihe: Methods in Molecular Biology

This detailed volume explores the latest methods that can be used to probe mRNA decay pathways and identify mRNA-binding protein targets as well as miRNA targets. Subjects include metabolic labelling and RNAseq methods for determining RNA decay rates, approaches for discovering RNA-binding protein targets, bioinformatics, miRNA targets and novel components of the miRNA-directed decay pathway, and recently developed approaches for studying nonsense-mediated mRNA decay, among other areas. Written for the highly popular Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.  Authoritative and practical, mRNA Decay: Methods and Protocols serves as an ideal guide for molecular biologists, geneticists, and developmental biologists with an interest in understanding how normal development and tissue homeostasis is regulated and how these processes are perturbed in inherited and acquired diseases.

Zielgruppe

Professional/practitioner

Autoren/Hrsg.

Lamandé, Shireen R.

Inhaltsverzeichnis

5'bromouridine IP Chase (BRIC)-Seq to Determine RNA Half Lives.- Determining mRNA Decay Rates Using RNA Approach to Equilibrium Sequencing (RATE-Seq).- Metabolic Labeling of Newly Synthesized RNA with 4sU to in Parallel Assess RNA Transcription and Decay.- Measuring mRNA Decay in Budding Yeast Using Single Molecule FISH.- PAR-CLIP for Discovering Target Sites of RNA-Binding Proteins.- Characterizing mRNA Sequence Motifs in the 3'UTR Using GFP Reporter Constructs.- iCLIP of the PIWI Protein Aubergine in Drosophila Embryos.- Integration of ENCODE RNAseq and eCLIP Data Sets.- Identifying miRNA Targets Using AgoRIP-Seq.- Integrated Analysis of miRNA and mRNA Expression Profiles to Identify miRNA Targets.- Identifying RISC Components Using Ago2 Immunoprecipitation and Mass Spectrometry.- Using Tet-Off Cells and RNAi Knockdown to Assay mRNA Decay.- Identifying Cellular Nonsense-Mediated mRNA Decay (NMD) Targets: Immunoprecipitation of Phosphorylated UPF1 Followed by RNA Sequencing(p-UPF1 RIP-Seq).- Generation of Cell Lines Stably Expressing a Fluorescent Reporter of Nonsense-Mediated mRNA Decay Activity.- Reactivation Assay to Identify Direct Targets of the Nonsense-Mediated mRNA Decay Pathway in Drosophila.-  Studying Nonsense-Mediated mRNA Decay in Mammalian Cells Using a Multicolored Bioluminescence-Based Reporter System.