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Aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases

The proliferation of antibiotic resistance has its origins in horizontal gene transfer. The class 1 integrons mediate gene transfer by assimilating antibiotic-resistance genes through site-specific recombination. For the class 1 integrons the first assimilated gene normally encodes an aminoglycoside...

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Autores principales: Zhang, Jun, Liu, Getong, Zhang, Xuhui, Chang, Yaowen, Wang, Shasha, He, Weizhi, Sun, Wenxia, Chen, Dongrong, Murchie, Alastair I.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588185/
https://www.ncbi.nlm.nih.gov/pubmed/33103573
http://dx.doi.org/10.1080/21505594.2020.1836910
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author Zhang, Jun
Liu, Getong
Zhang, Xuhui
Chang, Yaowen
Wang, Shasha
He, Weizhi
Sun, Wenxia
Chen, Dongrong
Murchie, Alastair I.H.
author_facet Zhang, Jun
Liu, Getong
Zhang, Xuhui
Chang, Yaowen
Wang, Shasha
He, Weizhi
Sun, Wenxia
Chen, Dongrong
Murchie, Alastair I.H.
author_sort Zhang, Jun
collection PubMed
description The proliferation of antibiotic resistance has its origins in horizontal gene transfer. The class 1 integrons mediate gene transfer by assimilating antibiotic-resistance genes through site-specific recombination. For the class 1 integrons the first assimilated gene normally encodes an aminoglycoside antibiotic resistance protein which is either an aminoglycoside acetyltransferase (AAC), nucleotidyltransferase – (ANT), or adenyl transferase (AAD). An aminoglycoside-sensing riboswitch RNA in the leader RNA of AAC/AAD that controls the expression of aminoglycoside resistance genes has been previously described. Here we explore the relationship between the recombinant products of integron recombination and a series of candidate riboswitch RNAs in the 5ʹ UTR of aad (aminoglycoside adenyltransferases) genes. The RNA sequences from the 5ʹ UTR of the aad genes from pathogenic strains that are the products of site-specific DNA recombination by class 1 integrons were investigated. Reporter assays, MicroScale Thermophoresis (MST) and covariance analysis revealed that a functional aminoglycoside-sensing riboswitch was selected at the DNA level through integron-mediated site-specific recombination. This study explains the close association between integron recombination and the aminoglycoside-sensing riboswitch RNA.
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spelling pubmed-75881852020-11-03 Aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases Zhang, Jun Liu, Getong Zhang, Xuhui Chang, Yaowen Wang, Shasha He, Weizhi Sun, Wenxia Chen, Dongrong Murchie, Alastair I.H. Virulence Research Paper The proliferation of antibiotic resistance has its origins in horizontal gene transfer. The class 1 integrons mediate gene transfer by assimilating antibiotic-resistance genes through site-specific recombination. For the class 1 integrons the first assimilated gene normally encodes an aminoglycoside antibiotic resistance protein which is either an aminoglycoside acetyltransferase (AAC), nucleotidyltransferase – (ANT), or adenyl transferase (AAD). An aminoglycoside-sensing riboswitch RNA in the leader RNA of AAC/AAD that controls the expression of aminoglycoside resistance genes has been previously described. Here we explore the relationship between the recombinant products of integron recombination and a series of candidate riboswitch RNAs in the 5ʹ UTR of aad (aminoglycoside adenyltransferases) genes. The RNA sequences from the 5ʹ UTR of the aad genes from pathogenic strains that are the products of site-specific DNA recombination by class 1 integrons were investigated. Reporter assays, MicroScale Thermophoresis (MST) and covariance analysis revealed that a functional aminoglycoside-sensing riboswitch was selected at the DNA level through integron-mediated site-specific recombination. This study explains the close association between integron recombination and the aminoglycoside-sensing riboswitch RNA. Taylor & Francis 2020-10-24 /pmc/articles/PMC7588185/ /pubmed/33103573 http://dx.doi.org/10.1080/21505594.2020.1836910 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Zhang, Jun
Liu, Getong
Zhang, Xuhui
Chang, Yaowen
Wang, Shasha
He, Weizhi
Sun, Wenxia
Chen, Dongrong
Murchie, Alastair I.H.
Aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases
title Aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases
title_full Aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases
title_fullStr Aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases
title_full_unstemmed Aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases
title_short Aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases
title_sort aminoglycoside riboswitch control of the expression of integron associated aminoglycoside resistance adenyltransferases
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588185/
https://www.ncbi.nlm.nih.gov/pubmed/33103573
http://dx.doi.org/10.1080/21505594.2020.1836910
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