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Eukaryotic Transcriptional and Post-Transcriptional Gene Expression Regulation

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Cover of 'Eukaryotic Transcriptional and Post-Transcriptional Gene Expression Regulation'

Table of Contents

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    Book Overview
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    Chapter 1 Fluorescence Reporter-Based Genome-Wide RNA Interference Screening to Identify Alternative Splicing Regulators.
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    Chapter 2 Tandem Affinity Purification Approach Coupled to Mass Spectrometry to Identify Post-translational Modifications of Histones Associated with Chromatin-Binding Proteins.
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    Chapter 3 Efficient Preparation of High-Complexity ChIP-Seq Profiles from Early Xenopus Embryos.
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    Chapter 4 Eukaryotic Transcriptional and Post-Transcriptional Gene Expression Regulation
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    Chapter 5 Assay for Transposase-Accessible Chromatin with High-Throughput Sequencing (ATAC-Seq) Protocol for Zebrafish Embryos.
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    Chapter 6 Establishment of Time- and Cell-Specific RNAi in Caenorhabditis elegans.
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    Chapter 7 Cell-Penetrating Peptide-Mediated Delivery of Cas9 Protein and Guide RNA for Genome Editing.
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    Chapter 8 Epigenetic Analysis of Endocrine Cell Subtypes from Human Pancreatic Islets.
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    Chapter 9 eIF3 Regulation of Protein Synthesis, Tumorigenesis, and Therapeutic Response.
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    Chapter 10 High-Resolution Gene Expression Profiling of RNA Synthesis, Processing, and Decay by Metabolic Labeling of Newly Transcribed RNA Using 4-Thiouridine.
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    Chapter 11 Accurate Detection of Differential Expression and Splicing Using Low-Level Features.
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    Chapter 12 Profiling Changes in Histone Post-translational Modifications by Top-Down Mass Spectrometry.
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    Chapter 13 Determining if an mRNA is a Substrate of Nonsense-Mediated mRNA Decay in Saccharomyces cerevisiae.
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    Chapter 14 Optimizing In Vitro Pre-mRNA 3' Cleavage Efficiency: Reconstitution from Anion-Exchange Separated HeLa Cleavage Factors and from Adherent HeLa Cell Nuclear Extract.
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    Chapter 15 Eukaryotic Transcriptional and Post-Transcriptional Gene Expression Regulation
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    Chapter 16 Using an Inducible CRISPR-dCas9-KRAB Effector System to Dissect Transcriptional Regulation in Human Embryonic Stem Cells.
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    Chapter 17 In Vitro Assay to Study Histone Ubiquitination During Transcriptional Regulation.
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    Chapter 18 Eukaryotic Transcriptional and Post-Transcriptional Gene Expression Regulation
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    Chapter 19 Large-Scale RNA Interference Screening to Identify Transcriptional Regulators of a Tumor Suppressor Gene.
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    Chapter 20 Transcriptional Analysis-Based Integrative Genomics Approach to Identify Tumor-Promoting Metabolic Genes.
Attention for Chapter 1: Fluorescence Reporter-Based Genome-Wide RNA Interference Screening to Identify Alternative Splicing Regulators.
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Chapter title
Fluorescence Reporter-Based Genome-Wide RNA Interference Screening to Identify Alternative Splicing Regulators.
Chapter number 1
Book title
Eukaryotic Transcriptional and Post-Transcriptional Gene Expression Regulation
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6518-2_1
Pubmed ID
Book ISBNs
978-1-4939-6516-8, 978-1-4939-6518-2
Authors

Ashish Misra, Michael R. Green

Editors

Narendra Wajapeyee, Romi Gupta

Abstract

Alternative splicing is a regulated process that leads to inclusion or exclusion of particular exons in a pre-mRNA transcript, resulting in multiple protein isoforms being encoded by a single gene. With more than 90 % of human genes known to undergo alternative splicing, it represents a major source for biological diversity inside cells. Although in vitro splicing assays have revealed insights into the mechanisms regulating individual alternative splicing events, our global understanding of alternative splicing regulation is still evolving. In recent years, genome-wide RNA interference (RNAi) screening has transformed biological research by enabling genome-scale loss-of-function screens in cultured cells and model organisms. In addition to resulting in the identification of new cellular pathways and potential drug targets, these screens have also uncovered many previously unknown mechanisms regulating alternative splicing. Here, we describe a method for the identification of alternative splicing regulators using genome-wide RNAi screening, as well as assays for further validation of the identified candidates. With modifications, this method can also be adapted to study the splicing regulation of pre-mRNAs that contain two or more splice isoforms.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 27%
Student > Bachelor 3 20%
Student > Ph. D. Student 2 13%
Professor 1 7%
Student > Master 1 7%
Other 3 20%
Unknown 1 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 7 47%
Biochemistry, Genetics and Molecular Biology 6 40%
Immunology and Microbiology 1 7%
Engineering 1 7%