| Literature DB >> 28766297 |
Angela Garibaldi1, Francisco Carranza1, Klemens J Hertel2.
Abstract
Isolation of newly transcribed RNA is an invaluable approach that can be used to study the dynamic life of RNA in cellulo. Traditional methods of whole-cell RNA extraction limit subsequent gene expression analyses to the steady-state levels of RNA abundance, which often masks changes in RNA synthesis and processing. This chapter describes a methodology with low cytotoxicity that permits the labeling and isolation of nascent pre-mRNA in cell culture. The resulting isolate is suitable for use in a series of downstream applications aimed at studying changes in RNA synthesis, processing, or stability.Entities:
Keywords: 4-Thiouridine; 4sU; 4sU-seq; Decay; Mammalian cells; Metabolic labeling; Nascent RNA; Nascent pre-mRNA; Transcription; mRNA processing
Mesh:
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Year: 2017 PMID: 28766297 PMCID: PMC5783291 DOI: 10.1007/978-1-4939-7204-3_13
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745