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Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae
Restriction-Modification systems (RMS) are one of the main mechanisms of defence against foreign DNA invasion and can have an important role in the regulation of gene expression. The obligate human pathogen Neisseria gonorrhoeae carries one of the highest loads of RMS in its genome; between 13 to 15...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789123/ https://www.ncbi.nlm.nih.gov/pubmed/31605008 http://dx.doi.org/10.1038/s41598-019-51102-2 |
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author | Sánchez-Busó, Leonor Golparian, Daniel Parkhill, Julian Unemo, Magnus Harris, Simon R. |
author_facet | Sánchez-Busó, Leonor Golparian, Daniel Parkhill, Julian Unemo, Magnus Harris, Simon R. |
author_sort | Sánchez-Busó, Leonor |
collection | PubMed |
description | Restriction-Modification systems (RMS) are one of the main mechanisms of defence against foreign DNA invasion and can have an important role in the regulation of gene expression. The obligate human pathogen Neisseria gonorrhoeae carries one of the highest loads of RMS in its genome; between 13 to 15 of the three main types. Previous work has described their organization in the reference genome FA1090 and has inferred the associated methylated motifs. Here, we studied the structure of RMS and target methylated motifs in 25 gonococcal strains sequenced with Single Molecule Real-Time (SMRT) technology, which provides data on DNA modification. The results showed a variable picture of active RMS in different strains, with phase variation switching the activity of Type III RMS, and both the activity and specificity of a Type I RMS. Interestingly, the Dam methylase was found in place of the NgoAXI endonuclease in two of the strains, despite being previously thought to be absent in the gonococcus. We also identified the real methylation target of NgoAXII as 5′-GCAGA-3′, different from that previously described. Results from this work give further insights into the diversity and dynamics of RMS and methylation patterns in N. gonorrhoeae. |
format | Online Article Text |
id | pubmed-6789123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67891232019-10-17 Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae Sánchez-Busó, Leonor Golparian, Daniel Parkhill, Julian Unemo, Magnus Harris, Simon R. Sci Rep Article Restriction-Modification systems (RMS) are one of the main mechanisms of defence against foreign DNA invasion and can have an important role in the regulation of gene expression. The obligate human pathogen Neisseria gonorrhoeae carries one of the highest loads of RMS in its genome; between 13 to 15 of the three main types. Previous work has described their organization in the reference genome FA1090 and has inferred the associated methylated motifs. Here, we studied the structure of RMS and target methylated motifs in 25 gonococcal strains sequenced with Single Molecule Real-Time (SMRT) technology, which provides data on DNA modification. The results showed a variable picture of active RMS in different strains, with phase variation switching the activity of Type III RMS, and both the activity and specificity of a Type I RMS. Interestingly, the Dam methylase was found in place of the NgoAXI endonuclease in two of the strains, despite being previously thought to be absent in the gonococcus. We also identified the real methylation target of NgoAXII as 5′-GCAGA-3′, different from that previously described. Results from this work give further insights into the diversity and dynamics of RMS and methylation patterns in N. gonorrhoeae. Nature Publishing Group UK 2019-10-11 /pmc/articles/PMC6789123/ /pubmed/31605008 http://dx.doi.org/10.1038/s41598-019-51102-2 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Sánchez-Busó, Leonor Golparian, Daniel Parkhill, Julian Unemo, Magnus Harris, Simon R. Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae |
title | Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae |
title_full | Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae |
title_fullStr | Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae |
title_full_unstemmed | Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae |
title_short | Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae |
title_sort | genetic variation regulates the activation and specificity of restriction-modification systems in neisseria gonorrhoeae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789123/ https://www.ncbi.nlm.nih.gov/pubmed/31605008 http://dx.doi.org/10.1038/s41598-019-51102-2 |
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