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Survey and Validation of tRNA Modifications and Their Corresponding Genes in Bacillus subtilis sp Subtilis Strain 168

Extensive knowledge of both the nature and position of tRNA modifications in all cellular tRNAs has been limited to two bacteria, Escherichia coli and Mycoplasma capricolum. Bacillus subtilis sp subtilis strain 168 is the model Gram-positive bacteria and the list of the genes involved in tRNA modifi...

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Autores principales: de Crécy-Lagard, Valérie, Ross, Robert L., Jaroch, Marshall, Marchand, Virginie, Eisenhart, Christina, Brégeon, Damien, Motorin, Yuri, Limbach, Patrick A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408541/
https://www.ncbi.nlm.nih.gov/pubmed/32629984
http://dx.doi.org/10.3390/biom10070977
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author de Crécy-Lagard, Valérie
Ross, Robert L.
Jaroch, Marshall
Marchand, Virginie
Eisenhart, Christina
Brégeon, Damien
Motorin, Yuri
Limbach, Patrick A.
author_facet de Crécy-Lagard, Valérie
Ross, Robert L.
Jaroch, Marshall
Marchand, Virginie
Eisenhart, Christina
Brégeon, Damien
Motorin, Yuri
Limbach, Patrick A.
author_sort de Crécy-Lagard, Valérie
collection PubMed
description Extensive knowledge of both the nature and position of tRNA modifications in all cellular tRNAs has been limited to two bacteria, Escherichia coli and Mycoplasma capricolum. Bacillus subtilis sp subtilis strain 168 is the model Gram-positive bacteria and the list of the genes involved in tRNA modifications in this organism is far from complete. Mass spectrometry analysis of bulk tRNA extracted from B. subtilis, combined with next generation sequencing technologies and comparative genomic analyses, led to the identification of 41 tRNA modification genes with associated confidence scores. Many differences were found in this model Gram-positive bacteria when compared to E. coli. In general, B. subtilis tRNAs are less modified than those in E. coli, even if some modifications, such as m(1)A22 or ms(2)t(6)A, are only found in the model Gram-positive bacteria. Many examples of non-orthologous displacements and of variations in the most complex pathways are described. Paralog issues make uncertain direct annotation transfer from E. coli to B. subtilis based on homology only without further experimental validation. This difficulty was shown with the identification of the B. subtilis enzyme that introduces ψ at positions 31/32 of the tRNAs. This work presents the most up to date list of tRNA modification genes in B. subtilis, identifies the gaps in knowledge, and lays the foundation for further work to decipher the physiological role of tRNA modifications in this important model organism and other bacteria.
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spelling pubmed-74085412020-08-13 Survey and Validation of tRNA Modifications and Their Corresponding Genes in Bacillus subtilis sp Subtilis Strain 168 de Crécy-Lagard, Valérie Ross, Robert L. Jaroch, Marshall Marchand, Virginie Eisenhart, Christina Brégeon, Damien Motorin, Yuri Limbach, Patrick A. Biomolecules Article Extensive knowledge of both the nature and position of tRNA modifications in all cellular tRNAs has been limited to two bacteria, Escherichia coli and Mycoplasma capricolum. Bacillus subtilis sp subtilis strain 168 is the model Gram-positive bacteria and the list of the genes involved in tRNA modifications in this organism is far from complete. Mass spectrometry analysis of bulk tRNA extracted from B. subtilis, combined with next generation sequencing technologies and comparative genomic analyses, led to the identification of 41 tRNA modification genes with associated confidence scores. Many differences were found in this model Gram-positive bacteria when compared to E. coli. In general, B. subtilis tRNAs are less modified than those in E. coli, even if some modifications, such as m(1)A22 or ms(2)t(6)A, are only found in the model Gram-positive bacteria. Many examples of non-orthologous displacements and of variations in the most complex pathways are described. Paralog issues make uncertain direct annotation transfer from E. coli to B. subtilis based on homology only without further experimental validation. This difficulty was shown with the identification of the B. subtilis enzyme that introduces ψ at positions 31/32 of the tRNAs. This work presents the most up to date list of tRNA modification genes in B. subtilis, identifies the gaps in knowledge, and lays the foundation for further work to decipher the physiological role of tRNA modifications in this important model organism and other bacteria. MDPI 2020-06-30 /pmc/articles/PMC7408541/ /pubmed/32629984 http://dx.doi.org/10.3390/biom10070977 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
de Crécy-Lagard, Valérie
Ross, Robert L.
Jaroch, Marshall
Marchand, Virginie
Eisenhart, Christina
Brégeon, Damien
Motorin, Yuri
Limbach, Patrick A.
Survey and Validation of tRNA Modifications and Their Corresponding Genes in Bacillus subtilis sp Subtilis Strain 168
title Survey and Validation of tRNA Modifications and Their Corresponding Genes in Bacillus subtilis sp Subtilis Strain 168
title_full Survey and Validation of tRNA Modifications and Their Corresponding Genes in Bacillus subtilis sp Subtilis Strain 168
title_fullStr Survey and Validation of tRNA Modifications and Their Corresponding Genes in Bacillus subtilis sp Subtilis Strain 168
title_full_unstemmed Survey and Validation of tRNA Modifications and Their Corresponding Genes in Bacillus subtilis sp Subtilis Strain 168
title_short Survey and Validation of tRNA Modifications and Their Corresponding Genes in Bacillus subtilis sp Subtilis Strain 168
title_sort survey and validation of trna modifications and their corresponding genes in bacillus subtilis sp subtilis strain 168
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408541/
https://www.ncbi.nlm.nih.gov/pubmed/32629984
http://dx.doi.org/10.3390/biom10070977
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