Literature DB >> 30276938

N6 -Methyladenosine-Sensitive RNA-Cleaving Deoxyribozymes.

Maksim V Sednev1, Volodymyr Mykhailiuk2,3, Priyanka Choudhury2,4, Julia Halang1, Katherine E Sloan4, Markus T Bohnsack2,4, Claudia Höbartner1,2.   

Abstract

Deoxyribozymes are synthetic enzymes made of DNA that can catalyze the cleavage or formation of phosphodiester bonds and are useful tools for RNA biochemistry. Herein, we report new RNA-cleaving deoxyribozymes to interrogate the methylation status of target RNAs, thereby providing an alternative method for the biochemical validation of RNA methylation sites containing N6 -methyladenosine, which is the most wide-spread and extensively investigated natural RNA modification. The developed deoxyribozymes are sensitive to the presence of N6 -methyladenosine in RNA near the cleavage site. One class of these DNA enzymes shows faster cleavage of methylated RNA, while others are strongly inhibited by the modified nucleotide. The general applicability of the new deoxyribozymes is demonstrated for several examples of natural RNA sequences, including a lncRNA and a set of C/D box snoRNAs, which have been suggested to contain m6 A as a regulatory element that influences RNA folding and protein binding.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  DNAzymes; N6-methyladenosine; RNA modification; deoxyribozymes; in vitro selection

Mesh:

Substances:

Year:  2018        PMID: 30276938     DOI: 10.1002/anie.201808745

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  8 in total

1.  Deoxyribozyme-based method for absolute quantification of N 6-methyladenosine fractions at specific sites of RNA.

Authors:  Magda Bujnowska; Jiacheng Zhang; Qing Dai; Emily M Heideman; Jingyi Fei
Journal:  J Biol Chem       Date:  2020-04-08       Impact factor: 5.157

Review 2.  Programmable technologies to manipulate gene expression at the RNA level.

Authors:  Huachun Liu; Simone Rauch; Bryan C Dickinson
Journal:  Curr Opin Chem Biol       Date:  2021-04-27       Impact factor: 8.972

3.  Sequence-specific m6A demethylation in RNA by FTO fused to RCas9.

Authors:  Kristina Rau; Lukas Rösner; Andrea Rentmeister
Journal:  RNA       Date:  2019-07-01       Impact factor: 4.942

4.  NOseq: amplicon sequencing evaluation method for RNA m6A sites after chemical deamination.

Authors:  Stephan Werner; Aurellia Galliot; Florian Pichot; Thomas Kemmer; Virginie Marchand; Maksim V Sednev; Tina Lence; Jean-Yves Roignant; Julian König; Claudia Höbartner; Yuri Motorin; Andreas Hildebrandt; Mark Helm
Journal:  Nucleic Acids Res       Date:  2021-02-26       Impact factor: 16.971

5.  The RNA methyltransferase METTL8 installs m3C32 in mitochondrial tRNAsThr/Ser(UCN) to optimise tRNA structure and mitochondrial translation.

Authors:  Nicole Kleiber; Nicolas Lemus-Diaz; Carina Stiller; Marleen Heinrichs; Mandy Mong-Quyen Mai; Philipp Hackert; Ricarda Richter-Dennerlein; Claudia Höbartner; Katherine E Bohnsack; Markus T Bohnsack
Journal:  Nat Commun       Date:  2022-01-11       Impact factor: 14.919

6.  Quick Access to Nucleobase-Modified Phosphoramidites for the Synthesis of Oligoribonucleotides Containing Post-Transcriptional Modifications and Epitranscriptomic Marks.

Authors:  Kamil Ziemkiewicz; Marcin Warminski; Radoslaw Wojcik; Joanna Kowalska; Jacek Jemielity
Journal:  J Org Chem       Date:  2022-07-20       Impact factor: 4.198

7.  LEAD-m6 A-seq for Locus-Specific Detection of N6 -Methyladenosine and Quantification of Differential Methylation.

Authors:  Yuru Wang; Zijie Zhang; Caraline Sepich-Poore; Lisheng Zhang; Yu Xiao; Chuan He
Journal:  Angew Chem Int Ed Engl       Date:  2020-11-10       Impact factor: 15.336

8.  N6 -Isopentenyladenosine in RNA Determines the Cleavage Site of Endonuclease Deoxyribozymes.

Authors:  Anam Liaqat; Carina Stiller; Manuela Michel; Maksim V Sednev; Claudia Höbartner
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-20       Impact factor: 16.823

  8 in total

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