| Literature DB >> 30701502 |
Shih-Shun Lin1, Yihua Chen2, Mei-Yeh Jade Lu3.
Abstract
Degradome sequencing provides large amounts of data regarding RNA degradation. The degradome library construction described here is modified from the 5'-rapid amplification of cDNA ends (5'-RACE), and each degradome cDNA is sequenced by next-generation sequencing (NGS). Degradome profiles provide information confirming miRNA-mediated cleavage of target genes and allow the identification of novel targets. Furthermore, degradome sequencing provides additional information for the study of RNA processing, such as information regarding RNA-binding proteins. In this chapter, we describe a detailed optimized protocol for constructing a degradome library with high yield and quality, along with NGS and data mining procedures. We hope that the degradome approach will be applied to further studies of non-model organisms.Keywords: 5′-RACE; Degradome; Next-generation sequencing; RNA degradation; Target RNA; microRNA
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Year: 2019 PMID: 30701502 DOI: 10.1007/978-1-4939-9042-9_15
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745