A Workflow Guide to RNA-Seq Analysis of Chaperone Function and Beyond

Methods Mol Biol. 2023:2693:39-60. doi: 10.1007/978-1-0716-3342-7_4.

Abstract

RNA sequencing (RNA-seq) is a powerful method of transcriptional analysis that allows for the sequence identification and quantification of cellular transcripts. RNA-seq can be used for differential gene expression (DGE) analysis, gene fusion detection, allele-specific expression, isoform and splice variant quantification, and identification of novel genes. These applications can be used for downstream systems biology analyses such as gene ontology or pathway analysis to provide insight into processes altered between biological conditions. Given the wide range of signaling pathways subject to chaperone activity as well as numerous chaperone functions in RNA metabolism, RNA-seq may provide a valuable tool for the study of chaperone proteins in biology and disease. This chapter outlines an example RNA-seq workflow to determine differentially expressed (DE) genes between two or more sample conditions and provides some considerations for RNA-seq experimental design.

Keywords: Chaperones; Differential gene expression analysis; Gene set enrichment analysis; Overrepresentation analysis; RNA-seq.

MeSH terms

  • Gene Expression Profiling / methods
  • High-Throughput Nucleotide Sequencing* / methods
  • Molecular Chaperones* / genetics
  • RNA-Seq
  • Sequence Analysis, RNA / methods
  • Transcriptome
  • Workflow

Substances

  • Molecular Chaperones