An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis

Bacteria possess elaborate systems to manage reactive oxygen and nitrogen species (ROS) arising from exposure to the mammalian immune system and environmental stresses. Here we report the discovery of an ROS-sensing RNA-modifying enzyme that regulates translation of stress-response proteins in the g...

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Main Authors: Lee, Wei Lin, Sinha, Ameya, Lam, Ling Ning, Loo, Hooi Linn, Liang, Jiaqi, Ho, Peiying, Cui, Liang, Chan, Cheryl Siew Choo, Begley, Thomas, Kline, Kimberly Ann, Dedon, Peter
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/171547
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Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-171547
record_format dspace
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences
Bactericidal Activity
Enterococcus Faecalis
spellingShingle Science::Biological sciences
Bactericidal Activity
Enterococcus Faecalis
Lee, Wei Lin
Sinha, Ameya
Lam, Ling Ning
Loo, Hooi Linn
Liang, Jiaqi
Ho, Peiying
Cui, Liang
Chan, Cheryl Siew Choo
Begley, Thomas
Kline, Kimberly Ann
Dedon, Peter
An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis
description Bacteria possess elaborate systems to manage reactive oxygen and nitrogen species (ROS) arising from exposure to the mammalian immune system and environmental stresses. Here we report the discovery of an ROS-sensing RNA-modifying enzyme that regulates translation of stress-response proteins in the gut commensal and opportunistic pathogen Enterococcus faecalis. We analyze the tRNA epitranscriptome of E. faecalis in response to reactive oxygen species (ROS) or sublethal doses of ROS-inducing antibiotics and identify large decreases in N2-methyladenosine (m2A) in both 23 S ribosomal RNA and transfer RNA. This we determine to be due to ROS-mediated inactivation of the Fe-S cluster-containing methyltransferase, RlmN. Genetic knockout of RlmN gives rise to a proteome that mimics the oxidative stress response, with an increase in levels of superoxide dismutase and decrease in virulence proteins. While tRNA modifications were established to be dynamic for fine-tuning translation, here we report the discovery of a dynamically regulated, environmentally responsive rRNA modification. These studies lead to a model in which RlmN serves as a redox-sensitive molecular switch, directly relaying oxidative stress to modulating translation through the rRNA and the tRNA epitranscriptome, adding a different paradigm in which RNA modifications can directly regulate the proteome.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Lee, Wei Lin
Sinha, Ameya
Lam, Ling Ning
Loo, Hooi Linn
Liang, Jiaqi
Ho, Peiying
Cui, Liang
Chan, Cheryl Siew Choo
Begley, Thomas
Kline, Kimberly Ann
Dedon, Peter
format Article
author Lee, Wei Lin
Sinha, Ameya
Lam, Ling Ning
Loo, Hooi Linn
Liang, Jiaqi
Ho, Peiying
Cui, Liang
Chan, Cheryl Siew Choo
Begley, Thomas
Kline, Kimberly Ann
Dedon, Peter
author_sort Lee, Wei Lin
title An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis
title_short An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis
title_full An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis
title_fullStr An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis
title_full_unstemmed An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis
title_sort rna modification enzyme directly senses reactive oxygen species for translational regulation in enterococcus faecalis
publishDate 2023
url https://hdl.handle.net/10356/171547
_version_ 1781793826542714880
spelling sg-ntu-dr.10356-1715472023-10-30T15:32:03Z An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis Lee, Wei Lin Sinha, Ameya Lam, Ling Ning Loo, Hooi Linn Liang, Jiaqi Ho, Peiying Cui, Liang Chan, Cheryl Siew Choo Begley, Thomas Kline, Kimberly Ann Dedon, Peter School of Biological Sciences School of Chemistry, Chemical Engineering and Biotechnology Antimicrobial Resistance IRG, Singapore MIT Alliance for Research and Technology Singapore Centre for Environmental Life Sciences and Engineering (SCELSE) Science::Biological sciences Bactericidal Activity Enterococcus Faecalis Bacteria possess elaborate systems to manage reactive oxygen and nitrogen species (ROS) arising from exposure to the mammalian immune system and environmental stresses. Here we report the discovery of an ROS-sensing RNA-modifying enzyme that regulates translation of stress-response proteins in the gut commensal and opportunistic pathogen Enterococcus faecalis. We analyze the tRNA epitranscriptome of E. faecalis in response to reactive oxygen species (ROS) or sublethal doses of ROS-inducing antibiotics and identify large decreases in N2-methyladenosine (m2A) in both 23 S ribosomal RNA and transfer RNA. This we determine to be due to ROS-mediated inactivation of the Fe-S cluster-containing methyltransferase, RlmN. Genetic knockout of RlmN gives rise to a proteome that mimics the oxidative stress response, with an increase in levels of superoxide dismutase and decrease in virulence proteins. While tRNA modifications were established to be dynamic for fine-tuning translation, here we report the discovery of a dynamically regulated, environmentally responsive rRNA modification. These studies lead to a model in which RlmN serves as a redox-sensitive molecular switch, directly relaying oxidative stress to modulating translation through the rRNA and the tRNA epitranscriptome, adding a different paradigm in which RNA modifications can directly regulate the proteome. Ministry of Education (MOE) National Research Foundation (NRF) Published version This research was supported by the National Research Foundation, Prime Minister’s Office, Singapore, under its Campus for Research Excellence and Technological Enterprise (CREATE) program, through the Singapore–MIT Alliance for Research and Technology Antimicrobial Resistance Interdisciplinary Research Group. We acknowledge funding support from NMRC OFIRG20nov-0079. Contributions of LNL were supported by the National Research Foundation and Ministry of Education Singapore under its Research Center of Excellence Program at SCELSE. A.S. and J.L. acknowledge support from the Singapore‐MIT Alliance (SMA) Graduate Fellowship and MOE Tier 2 Grant MOE2018-T2-2-13. Proteomics work was performed in part in the MIT Center for Environmental Health Sciences Bioanalytical Core, which is supported by Center grant P30‐ES002109 from the National Institute of Environmental Health Sciences with the aid of Dr. Michael Demott. 2023-10-30T06:04:54Z 2023-10-30T06:04:54Z 2023 Journal Article Lee, W. L., Sinha, A., Lam, L. N., Loo, H. L., Liang, J., Ho, P., Cui, L., Chan, C. S. C., Begley, T., Kline, K. A. & Dedon, P. (2023). An RNA modification enzyme directly senses reactive oxygen species for translational regulation in Enterococcus faecalis. Nature Communications, 14(1), 4093-. https://dx.doi.org/10.1038/s41467-023-39790-x 2041-1723 https://hdl.handle.net/10356/171547 10.1038/s41467-023-39790-x 37433804 2-s2.0-85164408063 1 14 4093 en NMRC OFIRG20nov-0079 MOE2018-T2-2-13 Nature Communications © The Author(s) 2023. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/ licenses/by/4.0/. application/pdf