CapZyme-Seq Comprehensively Defines Promoter-Sequence Determinants for RNA 5' Capping with NAD
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R01 GM041376
NIGMS NIH HHS - United States
R01 GM067005
NIGMS NIH HHS - United States
R35 GM118059
NIGMS NIH HHS - United States
R37 GM041376
NIGMS NIH HHS - United States
PubMed
29681497
PubMed Central
PMC5935523
DOI
10.1016/j.molcel.2018.03.014
PII: S1097-2765(18)30217-X
Knihovny.cz E-resources
- Keywords
- NudC, RNA capping, RNA polymerase, RNA-seq, Rai1, nicotinamide adenine dinucleotide, non-canonical initiating nucleotide, transcription, transcription initiation, transcription start site,
- MeSH
- DNA-Directed RNA Polymerases metabolism MeSH
- Endoribonucleases metabolism MeSH
- Escherichia coli genetics metabolism MeSH
- Gene Expression genetics MeSH
- Transcription, Genetic genetics MeSH
- NAD metabolism MeSH
- Nucleotides genetics MeSH
- Transcription Initiation Site physiology MeSH
- Promoter Regions, Genetic genetics MeSH
- RNA Caps genetics MeSH
- Transcriptome genetics MeSH
- High-Throughput Nucleotide Sequencing methods MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- DNA-Directed RNA Polymerases MeSH
- Endoribonucleases MeSH
- mRNA decapping enzymes MeSH Browser
- NAD MeSH
- Nucleotides MeSH
- RNA Caps MeSH
Nucleoside-containing metabolites such as NAD+ can be incorporated as 5' caps on RNA by serving as non-canonical initiating nucleotides (NCINs) for transcription initiation by RNA polymerase (RNAP). Here, we report CapZyme-seq, a high-throughput-sequencing method that employs NCIN-decapping enzymes NudC and Rai1 to detect and quantify NCIN-capped RNA. By combining CapZyme-seq with multiplexed transcriptomics, we determine efficiencies of NAD+ capping by Escherichia coli RNAP for ∼16,000 promoter sequences. The results define preferred transcription start site (TSS) positions for NAD+ capping and define a consensus promoter sequence for NAD+ capping: HRRASWW (TSS underlined). By applying CapZyme-seq to E. coli total cellular RNA, we establish that sequence determinants for NCIN capping in vivo match the NAD+-capping consensus defined in vitro, and we identify and quantify NCIN-capped small RNAs (sRNAs). Our findings define the promoter-sequence determinants for NCIN capping with NAD+ and provide a general method for analysis of NCIN capping in vitro and in vivo.
Department of Cell Biology and Neuroscience Rutgers University Piscataway NJ 08854 USA
Department of Chemistry and Waksman Institute Rutgers University Piscataway NJ 08854 USA
Department of Genetics and Waksman Institute Rutgers University Piscataway NJ 08854 USA
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