Cargando…
Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability
Mesorhizobium loti contains ten genes coding for proteins sharing high amino acid sequence identity with members of the Ros/MucR transcription factor family. Five of these Ros/MucR family members from Mesorhizobium loti (Ml proteins) have been recently structurally and functionally characterized dem...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693944/ https://www.ncbi.nlm.nih.gov/pubmed/29150637 http://dx.doi.org/10.1038/s41598-017-16127-5 |
_version_ | 1783280021759066112 |
---|---|
author | Baglivo, Ilaria Pirone, Luciano Pedone, Emilia Maria Pitzer, Joshua Edison Muscariello, Lidia Marino, Maria Michela Malgieri, Gaetano Freschi, Andrea Chambery, Angela Roop II, Roy-Martin Pedone, Paolo Vincenzo |
author_facet | Baglivo, Ilaria Pirone, Luciano Pedone, Emilia Maria Pitzer, Joshua Edison Muscariello, Lidia Marino, Maria Michela Malgieri, Gaetano Freschi, Andrea Chambery, Angela Roop II, Roy-Martin Pedone, Paolo Vincenzo |
author_sort | Baglivo, Ilaria |
collection | PubMed |
description | Mesorhizobium loti contains ten genes coding for proteins sharing high amino acid sequence identity with members of the Ros/MucR transcription factor family. Five of these Ros/MucR family members from Mesorhizobium loti (Ml proteins) have been recently structurally and functionally characterized demonstrating that Ml proteins are DNA-binding proteins. However, the DNA-binding studies were performed using the Ros DNA-binding site with the Ml proteins. Currently, there is no evidence as to when the Ml proteins are expressed during the Mesorhizobium lo ti life cycle as well as no information concerning their natural DNA-binding site. In this study, we examine the ml genes expression profile in Mesorhizobium loti and show that ml1, ml2, ml3 and ml5 are expressed during planktonic growth and in biofilms. DNA-binding experiments show that the Ml proteins studied bind a conserved AT-rich site in the promoter region of the exoY gene from Mesorhizobium loti and that the proteins make important contacts with the minor groove of DNA. Moreover, we demonstrate that the Ml proteins studied form higher-order oligomers through their N-terminal region and that the same AT-rich site is recognized by MucR from Brucella abortus using a similar mechanism involving contacts with the minor groove of DNA and oligomerization. |
format | Online Article Text |
id | pubmed-5693944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56939442017-11-27 Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability Baglivo, Ilaria Pirone, Luciano Pedone, Emilia Maria Pitzer, Joshua Edison Muscariello, Lidia Marino, Maria Michela Malgieri, Gaetano Freschi, Andrea Chambery, Angela Roop II, Roy-Martin Pedone, Paolo Vincenzo Sci Rep Article Mesorhizobium loti contains ten genes coding for proteins sharing high amino acid sequence identity with members of the Ros/MucR transcription factor family. Five of these Ros/MucR family members from Mesorhizobium loti (Ml proteins) have been recently structurally and functionally characterized demonstrating that Ml proteins are DNA-binding proteins. However, the DNA-binding studies were performed using the Ros DNA-binding site with the Ml proteins. Currently, there is no evidence as to when the Ml proteins are expressed during the Mesorhizobium lo ti life cycle as well as no information concerning their natural DNA-binding site. In this study, we examine the ml genes expression profile in Mesorhizobium loti and show that ml1, ml2, ml3 and ml5 are expressed during planktonic growth and in biofilms. DNA-binding experiments show that the Ml proteins studied bind a conserved AT-rich site in the promoter region of the exoY gene from Mesorhizobium loti and that the proteins make important contacts with the minor groove of DNA. Moreover, we demonstrate that the Ml proteins studied form higher-order oligomers through their N-terminal region and that the same AT-rich site is recognized by MucR from Brucella abortus using a similar mechanism involving contacts with the minor groove of DNA and oligomerization. Nature Publishing Group UK 2017-11-17 /pmc/articles/PMC5693944/ /pubmed/29150637 http://dx.doi.org/10.1038/s41598-017-16127-5 Text en © The Author(s) 2017 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 Baglivo, Ilaria Pirone, Luciano Pedone, Emilia Maria Pitzer, Joshua Edison Muscariello, Lidia Marino, Maria Michela Malgieri, Gaetano Freschi, Andrea Chambery, Angela Roop II, Roy-Martin Pedone, Paolo Vincenzo Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability |
title | Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability |
title_full | Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability |
title_fullStr | Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability |
title_full_unstemmed | Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability |
title_short | Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability |
title_sort | ml proteins from mesorhizobium loti and mucr from brucella abortus: an at-rich core dna-target site and oligomerization ability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693944/ https://www.ncbi.nlm.nih.gov/pubmed/29150637 http://dx.doi.org/10.1038/s41598-017-16127-5 |
work_keys_str_mv | AT baglivoilaria mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT pironeluciano mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT pedoneemiliamaria mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT pitzerjoshuaedison mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT muscariellolidia mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT marinomariamichela mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT malgierigaetano mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT freschiandrea mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT chamberyangela mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT roopiiroymartin mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability AT pedonepaolovincenzo mlproteinsfrommesorhizobiumlotiandmucrfrombrucellaabortusanatrichcorednatargetsiteandoligomerizationability |