Metabolic labeling of RNA using multiple ribonucleoside analogs enables the simultaneous evaluation of RNA synthesis and degradation rates

• Published in: Genome research Vol. 30; no. 10; pp. 1481 - 1491
• Main Authors: Kawata, Kentaro, Wakida, Hiroyasu, Yamada, Toshimichi, Taniue, Kenzui, Han, Han, Seki, Masahide, Suzuki, Yutaka, Akimitsu, Nobuyoshi
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 01.10.2020
• Subjects: Degradation; External stimuli; Gene expression; Method; Transcription
• ISSN: 1088-9051; 1549-5469
• DOI: 10.1101/gr.264408.120

Gene expression is determined by a balance between RNA synthesis and RNA degradation. To elucidate the underlying regulatory mechanisms and principles of this, simultaneous measurements of RNA synthesis and degradation are required. Here, we report the development of "Dyrec-seq," which uses 4-thiouridine and 5-bromouridine to simultaneously quantify RNA synthesis and degradation rates. Dyrec-seq enabled the quantification of RNA synthesis and degradation rates of 4702 genes in HeLa cells. Functional enrichment analysis showed that the RNA synthesis and degradation rates of genes are actually determined by the genes' biological functions. A comparison of theoretical and experimental analyses revealed that the amount of RNA is determined by the ratio of RNA synthesis to degradation rates, whereas the rapidity of responses to external stimuli is determined only by the degradation rate. This study emphasizes that not only RNA synthesis but also RNA degradation is important in shaping gene expression patterns.