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Thioguanosine Conversion Enables mRNA-Lifetime Evaluation by RNA Sequencing Using Double Metabolic Labeling (TUC-seq DUAL).

Authors :
Gasser C
Delazer I
Neuner E
Pascher K
Brillet K
Klotz S
Trixl L
Himmelstoß M
Ennifar E
Rieder D
Lusser A
Micura R
Source :
Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2020 Apr 20; Vol. 59 (17), pp. 6881-6886. Date of Electronic Publication: 2020 Feb 28.
Publication Year :
2020

Abstract

Temporal information about cellular RNA populations is essential to understand the functional roles of RNA. We have developed the hydrazine/NH <subscript>4</subscript> Cl/OsO <subscript>4</subscript> -based conversion of 6-thioguanosine (6sG) into A', where A' constitutes a 6-hydrazino purine derivative. A' retains the Watson-Crick base-pair mode and is efficiently decoded as adenosine in primer extension assays and in RNA sequencing. Because 6sG is applicable to metabolic labeling of freshly synthesized RNA and because the conversion chemistry is fully compatible with the conversion of the frequently used metabolic label 4-thiouridine (4sU) into C, the combination of both modified nucleosides in dual-labeling setups enables high accuracy measurements of RNA decay. This approach, termed TUC-seq DUAL, uses the two modified nucleosides in subsequent pulses and their simultaneous detection, enabling mRNA-lifetime evaluation with unprecedented precision.<br /> (© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.)

Details

Language :
English
ISSN :
1521-3773
Volume :
59
Issue :
17
Database :
MEDLINE
Journal :
Angewandte Chemie (International ed. in English)
Publication Type :
Academic Journal
Accession number :
31999864
Full Text :
https://doi.org/10.1002/anie.201916272