Cargando…
High pressure activation of the Mrr restriction endonuclease in Escherichia coli involves tetramer dissociation
A sub-lethal hydrostatic pressure (HP) shock of ∼100 MPa elicits a RecA-dependent DNA damage (SOS) response in Escherichia coli K-12, despite the fact that pressure cannot compromise the covalent integrity of DNA. Prior screens for HP resistance identified Mrr (Methylated adenine Recognition and Res...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435990/ https://www.ncbi.nlm.nih.gov/pubmed/28369499 http://dx.doi.org/10.1093/nar/gkx192 |
_version_ | 1783237323081646080 |
---|---|
author | Bourges, Anaïs C. Torres Montaguth, Oscar E. Ghosh, Anirban Tadesse, Wubishet M. Declerck, Nathalie Aertsen, Abram Royer, Catherine A. |
author_facet | Bourges, Anaïs C. Torres Montaguth, Oscar E. Ghosh, Anirban Tadesse, Wubishet M. Declerck, Nathalie Aertsen, Abram Royer, Catherine A. |
author_sort | Bourges, Anaïs C. |
collection | PubMed |
description | A sub-lethal hydrostatic pressure (HP) shock of ∼100 MPa elicits a RecA-dependent DNA damage (SOS) response in Escherichia coli K-12, despite the fact that pressure cannot compromise the covalent integrity of DNA. Prior screens for HP resistance identified Mrr (Methylated adenine Recognition and Restriction), a Type IV restriction endonuclease (REase), as instigator for this enigmatic HP-induced SOS response. Type IV REases tend to target modified DNA sites, and E. coli Mrr activity was previously shown to be elicited by expression of the foreign M.HhaII Type II methytransferase (MTase), as well. Here we measured the concentration and stoichiometry of a functional GFP-Mrr fusion protein using in vivo fluorescence fluctuation microscopy. Our results demonstrate that Mrr is a tetramer in unstressed cells, but shifts to a dimer after HP shock or co-expression with M.HhaII. Based on the differences in reversibility of tetramer dissociation observed for wild-type GFP-Mrr and a catalytic mutant upon HP shock compared to M.HhaII expression, we propose a model by which (i) HP triggers Mrr activity by directly pushing inactive Mrr tetramers to dissociate into active Mrr dimers, while (ii) M.HhaII triggers Mrr activity by creating high affinity target sites on the chromosome, which pull the equilibrium from inactive tetrameric Mrr toward active dimer. |
format | Online Article Text |
id | pubmed-5435990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54359902017-05-22 High pressure activation of the Mrr restriction endonuclease in Escherichia coli involves tetramer dissociation Bourges, Anaïs C. Torres Montaguth, Oscar E. Ghosh, Anirban Tadesse, Wubishet M. Declerck, Nathalie Aertsen, Abram Royer, Catherine A. Nucleic Acids Res Nucleic Acid Enzymes A sub-lethal hydrostatic pressure (HP) shock of ∼100 MPa elicits a RecA-dependent DNA damage (SOS) response in Escherichia coli K-12, despite the fact that pressure cannot compromise the covalent integrity of DNA. Prior screens for HP resistance identified Mrr (Methylated adenine Recognition and Restriction), a Type IV restriction endonuclease (REase), as instigator for this enigmatic HP-induced SOS response. Type IV REases tend to target modified DNA sites, and E. coli Mrr activity was previously shown to be elicited by expression of the foreign M.HhaII Type II methytransferase (MTase), as well. Here we measured the concentration and stoichiometry of a functional GFP-Mrr fusion protein using in vivo fluorescence fluctuation microscopy. Our results demonstrate that Mrr is a tetramer in unstressed cells, but shifts to a dimer after HP shock or co-expression with M.HhaII. Based on the differences in reversibility of tetramer dissociation observed for wild-type GFP-Mrr and a catalytic mutant upon HP shock compared to M.HhaII expression, we propose a model by which (i) HP triggers Mrr activity by directly pushing inactive Mrr tetramers to dissociate into active Mrr dimers, while (ii) M.HhaII triggers Mrr activity by creating high affinity target sites on the chromosome, which pull the equilibrium from inactive tetrameric Mrr toward active dimer. Oxford University Press 2017-05-19 2017-03-21 /pmc/articles/PMC5435990/ /pubmed/28369499 http://dx.doi.org/10.1093/nar/gkx192 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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 Bourges, Anaïs C. Torres Montaguth, Oscar E. Ghosh, Anirban Tadesse, Wubishet M. Declerck, Nathalie Aertsen, Abram Royer, Catherine A. High pressure activation of the Mrr restriction endonuclease in Escherichia coli involves tetramer dissociation |
title | High pressure activation of the Mrr restriction endonuclease in Escherichia coli involves tetramer dissociation |
title_full | High pressure activation of the Mrr restriction endonuclease in Escherichia coli involves tetramer dissociation |
title_fullStr | High pressure activation of the Mrr restriction endonuclease in Escherichia coli involves tetramer dissociation |
title_full_unstemmed | High pressure activation of the Mrr restriction endonuclease in Escherichia coli involves tetramer dissociation |
title_short | High pressure activation of the Mrr restriction endonuclease in Escherichia coli involves tetramer dissociation |
title_sort | high pressure activation of the mrr restriction endonuclease in escherichia coli involves tetramer dissociation |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435990/ https://www.ncbi.nlm.nih.gov/pubmed/28369499 http://dx.doi.org/10.1093/nar/gkx192 |
work_keys_str_mv | AT bourgesanaisc highpressureactivationofthemrrrestrictionendonucleaseinescherichiacoliinvolvestetramerdissociation AT torresmontaguthoscare highpressureactivationofthemrrrestrictionendonucleaseinescherichiacoliinvolvestetramerdissociation AT ghoshanirban highpressureactivationofthemrrrestrictionendonucleaseinescherichiacoliinvolvestetramerdissociation AT tadessewubishetm highpressureactivationofthemrrrestrictionendonucleaseinescherichiacoliinvolvestetramerdissociation AT declercknathalie highpressureactivationofthemrrrestrictionendonucleaseinescherichiacoliinvolvestetramerdissociation AT aertsenabram highpressureactivationofthemrrrestrictionendonucleaseinescherichiacoliinvolvestetramerdissociation AT royercatherinea highpressureactivationofthemrrrestrictionendonucleaseinescherichiacoliinvolvestetramerdissociation |