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  A Novel NAD-RNA Decapping Pathway Discovered by Synthetic Light-Up NAD-RNAs

Abele, F., Höfer, K., Bernhard, P., Grawenhoff, J., Seidel, M., Krause, A., et al. (2020). A Novel NAD-RNA Decapping Pathway Discovered by Synthetic Light-Up NAD-RNAs. Biomolecules, 10(4). doi:10.3390/biom10040513.

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https://www.ncbi.nlm.nih.gov/pubmed/32231086 (beliebiger Volltext)
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 Urheber:
Abele, F., Autor
Höfer, K.1, Autor           
Bernhard, P., Autor
Grawenhoff, J., Autor
Seidel, M., Autor
Krause, A., Autor
Kopf, S., Autor
Schröter, M., Autor
Jäschke, A., Autor
Affiliations:
1Institute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, ou_persistent22              

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Schlagwörter: ADP-ribosyl Cyclase 1/genetics/*metabolism Adenosine/chemistry Biochemistry/methods Endoribonucleases/genetics/metabolism Fluorescence Kinetics Membrane Glycoproteins/genetics/*metabolism NAD/genetics/*metabolism Oligonucleotides/chemical synthesis RNA Caps/chemistry/genetics/*metabolism Spectrometry, Fluorescence *Decapping *NAD metabolism *NAD-capped RNA *RNA modification *fluorescent RNA *glycohydrolase *high-throughput screening
 Zusammenfassung: The complexity of the transcriptome is governed by the intricate interplay of transcription, RNA processing, translocation, and decay. In eukaryotes, the removal of the 5'-RNA cap is essential for the initiation of RNA degradation. In addition to the canonical 5'-N7-methyl guanosine cap in eukaryotes, the ubiquitous redox cofactor nicotinamide adenine dinucleotide (NAD) was identified as a new 5'-RNA cap structure in prokaryotic and eukaryotic organisms. So far, two classes of NAD-RNA decapping enzymes have been identified, namely Nudix enzymes that liberate nicotinamide mononucleotide (NMN) and DXO-enzymes that remove the entire NAD cap. Herein, we introduce 8-(furan-2-yl)-substituted NAD-capped-RNA ((Fur)NAD-RNA) as a new research tool for the identification and characterization of novel NAD-RNA decapping enzymes. These compounds are found to be suitable for various enzymatic reactions that result in the release of a fluorescence quencher, either nicotinamide (NAM) or nicotinamide mononucleotide (NMN), from the RNA which causes a fluorescence turn-on. (Fur)NAD-RNAs allow for real-time quantification of decapping activity, parallelization, high-throughput screening and identification of novel decapping enzymes in vitro. Using (Fur)NAD-RNAs, we discovered that the eukaryotic glycohydrolase CD38 processes NAD-capped RNA in vitro into ADP-ribose-modified-RNA and nicotinamide and therefore might act as a decapping enzyme in vivo. The existence of multiple pathways suggests that the decapping of NAD-RNA is an important and regulated process in eukaryotes.

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 Datum: 2020-04-02
 Publikationsstatus: Erschienen
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 Art der Begutachtung: -
 Identifikatoren: Anderer: 32231086
DOI: 10.3390/biom10040513
ISSN: 2218-273X (Electronic)2218-273X (Linking)
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Titel: Biomolecules
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 10 (4) Artikelnummer: - Start- / Endseite: - Identifikator: -