Chapter title |
Genome-Wide Analysis of Long Noncoding RNA Turnover.
|
---|---|
Chapter number | 19 |
Book title |
Nuclear Bodies and Noncoding RNAs
|
Published in |
Methods in molecular biology, January 2015
|
DOI | 10.1007/978-1-4939-2253-6_19 |
Pubmed ID | |
Book ISBNs |
978-1-4939-2252-9, 978-1-4939-2253-6
|
Authors |
Tani H, Imamachi N, Mizutani R, Imamura K, Kwon Y, Miyazaki S, Maekawa S, Suzuki Y, Akimitsu N, Hidenori Tani, Naoto Imamachi, Rena Mizutani, Katsutoshi Imamura, Yeondae Kwon, Satoru Miyazaki, Sho Maekawa, Yutaka Suzuki, Nobuyoshi Akimitsu, Tani, Hidenori, Imamachi, Naoto, Mizutani, Rena, Imamura, Katsutoshi, Kwon, Yeondae, Miyazaki, Satoru, Maekawa, Sho, Suzuki, Yutaka, Akimitsu, Nobuyoshi |
Abstract |
Genome-wide analysis for determining RNA turnover is an advanced method in RNA biology that examines the specific half-life of nuclear noncoding RNA (ncRNA). In particular, a pulse-labeling method using uridine analogs enables the determination of RNA stability under physiologically undisturbed conditions. The technique involves pulse labeling of endogenous RNAs in mammalian cells with 5'-bromo-uridine (BrU), followed by measuring the chronological decrease of BrU-labeled RNAs using deep sequencing. The method is called BrU immunoprecipitation chase assay (BRIC) or BRIC through deep sequencing (BRIC-seq). Here, we describe a detailed protocol and technical tips for BRIC-seq. |
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