Metabolic RNA labeling for probing RNA dynamics in bacteria

Author:

Meng Liying12,Guo Yilan13,Tang Qi13,Huang Rongbing13,Xie Yuchen12,Chen Xing12345ORCID

Affiliation:

1. College of Chemistry and Molecular Engineering, Peking University, Beijing, China

2. Peking-Tsinghua Center for Life Sciences, Peking University, Beijing, China

3. Beijing National Laboratory for Molecular Sciences, Peking University, Beijing, China

4. Synthetic and Functional Biomolecules Center, Peking University, Beijing, China

5. Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Peking University, Beijing, China

Abstract

Abstract Metabolic labeling of RNAs with noncanonical nucleosides that are chemically active, followed by chemoselective conjugation with imaging probes or enrichment tags, has emerged as a powerful method for studying RNA transcription and degradation in eukaryotes. However, metabolic RNA labeling is not applicable for prokaryotes, in which the complexity and distinctness of gene regulation largely remain to be explored. Here, we report 2′-deoxy-2′-azidoguanosine (AzG) as a noncanonical nucleoside compatible with metabolic labeling of bacterial RNAs. With AzG, we develop AIR-seq (azidonucleoside-incorporated RNA sequencing), which enables genome-wide analysis of transcription upon heat stress in Escherichia coli. Furthermore, AIR-seq coupled with pulse-chase labeling allows for global analysis of bacterial RNA degradation. Finally, we demonstrate that RNAs of mouse gut microbiotas can be metabolically labeled with AzG in living animals. The AzG-enabled metabolic RNA labeling should find broad applications in studying RNA biology in various bacterial species.

Funder

National Key Research and Development

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Genetics

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