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A programmable pAgo nuclease with RNA target preference from the psychrotolerant bacterium Mucilaginibacter paludis

Argonaute (Ago) proteins are programmable nucleases found in eukaryotes and prokaryotes. Prokaryotic Agos (pAgos) share a high degree of structural homology with eukaryotic Agos (eAgos), and eAgos originate from pAgos. Although eAgos exclusively cleave RNA targets, most characterized pAgos cleave DN...

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Autores principales: Li, Wenqiang, Liu, Yang, He, Ruyi, Wang, Longyu, Wang, Yaping, Zeng, Wanting, Zhang, Zhiwei, Wang, Fei, Ma, Lixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122594/
https://www.ncbi.nlm.nih.gov/pubmed/35524569
http://dx.doi.org/10.1093/nar/gkac315
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author Li, Wenqiang
Liu, Yang
He, Ruyi
Wang, Longyu
Wang, Yaping
Zeng, Wanting
Zhang, Zhiwei
Wang, Fei
Ma, Lixin
author_facet Li, Wenqiang
Liu, Yang
He, Ruyi
Wang, Longyu
Wang, Yaping
Zeng, Wanting
Zhang, Zhiwei
Wang, Fei
Ma, Lixin
author_sort Li, Wenqiang
collection PubMed
description Argonaute (Ago) proteins are programmable nucleases found in eukaryotes and prokaryotes. Prokaryotic Agos (pAgos) share a high degree of structural homology with eukaryotic Agos (eAgos), and eAgos originate from pAgos. Although eAgos exclusively cleave RNA targets, most characterized pAgos cleave DNA targets. This study characterized a novel pAgo, MbpAgo, from the psychrotolerant bacterium Mucilaginibacter paludis which prefers to cleave RNA targets rather than DNA targets. Compared to previously studied Agos, MbpAgo can utilize both 5′phosphorylated(5′P) and 5′hydroxylated(5′OH) DNA guides (gDNAs) to efficiently cleave RNA targets at the canonical cleavage site if the guide is between 15 and 17 nt long. Furthermore, MbpAgo is active at a wide range of temperatures (4–65°C) and displays no obvious preference for the 5′-nucleotide of a guide. Single-nucleotide and most dinucleotide mismatches have no or little effects on cleavage efficiency, except for dinucleotide mismatches at positions 11–13 that dramatically reduce target cleavage. MbpAgo can efficiently cleave highly structured RNA targets using both 5′P and 5′OH gDNAs in the presence of Mg(2+) or Mn(2+). The biochemical characterization of MbpAgo paves the way for its use in RNA manipulations such as nucleic acid detection and clearance of RNA viruses.
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spelling pubmed-91225942022-05-23 A programmable pAgo nuclease with RNA target preference from the psychrotolerant bacterium Mucilaginibacter paludis Li, Wenqiang Liu, Yang He, Ruyi Wang, Longyu Wang, Yaping Zeng, Wanting Zhang, Zhiwei Wang, Fei Ma, Lixin Nucleic Acids Res Nucleic Acid Enzymes Argonaute (Ago) proteins are programmable nucleases found in eukaryotes and prokaryotes. Prokaryotic Agos (pAgos) share a high degree of structural homology with eukaryotic Agos (eAgos), and eAgos originate from pAgos. Although eAgos exclusively cleave RNA targets, most characterized pAgos cleave DNA targets. This study characterized a novel pAgo, MbpAgo, from the psychrotolerant bacterium Mucilaginibacter paludis which prefers to cleave RNA targets rather than DNA targets. Compared to previously studied Agos, MbpAgo can utilize both 5′phosphorylated(5′P) and 5′hydroxylated(5′OH) DNA guides (gDNAs) to efficiently cleave RNA targets at the canonical cleavage site if the guide is between 15 and 17 nt long. Furthermore, MbpAgo is active at a wide range of temperatures (4–65°C) and displays no obvious preference for the 5′-nucleotide of a guide. Single-nucleotide and most dinucleotide mismatches have no or little effects on cleavage efficiency, except for dinucleotide mismatches at positions 11–13 that dramatically reduce target cleavage. MbpAgo can efficiently cleave highly structured RNA targets using both 5′P and 5′OH gDNAs in the presence of Mg(2+) or Mn(2+). The biochemical characterization of MbpAgo paves the way for its use in RNA manipulations such as nucleic acid detection and clearance of RNA viruses. Oxford University Press 2022-05-07 /pmc/articles/PMC9122594/ /pubmed/35524569 http://dx.doi.org/10.1093/nar/gkac315 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Nucleic Acid Enzymes
Li, Wenqiang
Liu, Yang
He, Ruyi
Wang, Longyu
Wang, Yaping
Zeng, Wanting
Zhang, Zhiwei
Wang, Fei
Ma, Lixin
A programmable pAgo nuclease with RNA target preference from the psychrotolerant bacterium Mucilaginibacter paludis
title A programmable pAgo nuclease with RNA target preference from the psychrotolerant bacterium Mucilaginibacter paludis
title_full A programmable pAgo nuclease with RNA target preference from the psychrotolerant bacterium Mucilaginibacter paludis
title_fullStr A programmable pAgo nuclease with RNA target preference from the psychrotolerant bacterium Mucilaginibacter paludis
title_full_unstemmed A programmable pAgo nuclease with RNA target preference from the psychrotolerant bacterium Mucilaginibacter paludis
title_short A programmable pAgo nuclease with RNA target preference from the psychrotolerant bacterium Mucilaginibacter paludis
title_sort programmable pago nuclease with rna target preference from the psychrotolerant bacterium mucilaginibacter paludis
topic Nucleic Acid Enzymes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122594/
https://www.ncbi.nlm.nih.gov/pubmed/35524569
http://dx.doi.org/10.1093/nar/gkac315
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