English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/88209
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

Title

Nicking activity of the pMV158 MobM relaxase on cognate and heterologous origins of transfer

AuthorsFernández-López, Cris ; Lorenzo-Díaz, Fabián ; Pérez-Luque, Rosa ; Rodríguez-González, Lorena ; Boer, Roeland ; Lurz, Rudi; Bravo, Alicia ; Coll, Miquel ; Espinosa, Manuel
KeywordsOrigin of transfer
Rolling circle-replicating plasmids
DNA relaxase
DNA–protein interactions
Issue Date2013
PublisherElsevier
CitationPlasmid 70(1): 120-130 (2013)
AbstractThe MobM relaxase (494 amino acids) encoded by the promiscuous streptococcal plasmid pMV158 recognizes the plasmid origin of transfer, oriTpMV158, and converts supercoiled pMV158 DNA into relaxed molecules by cleavage of the phosphodiester bond of a specific dinucleotide within the sequence 5'-GTGTG/TT-3' (>/> being the nick site). After cleavage, the protein remains stably bound to the 5'-end of the nick site. Band-shift assays with single-stranded oligonucleotides and size-exclusion chromatography allowed us to show that MobM was able to generate specific complexes with one of the inverted repeats of the oriTpMV158, presumably extruded as stem-loop structure. A number of tests have been performed to attain a better characterization of the nicking activity of MobM and its linkage with its target DNA. The optimal pH for DNA relaxation was found to be 6.5. Upon nicking, gel retardation assays showed that MobM formed stable complexes with its target DNA. Moreover, MobM bound to relaxed pMV158 molecules were visualized by electron microscopy. The staphylococcal plasmids pUB110 and pE194, and the streptococcal plasmid pDL287 harbour putative oriTs and may encode Mob proteins homologous to MobM. The oriTpUB110, oriTpDL287, and oriTpE194 sequences share 100%, 70%, and 67% (in a 43-nucleotide stretch and allowing a 3-bp gap) identity to oriTpMV158, respectively. Nicking assays using supercoiled DNAs from pUB110, pDL287, and pE194 showed that MobM was able to relax, to differing degrees, all plasmid DNAs. Our results suggest that cross-recognition of heterologous oriTs by Mob proteins could play an important role in the plasmid spreading between bacteria. © 2013 Elsevier Inc.
Publisher version (URL)http://dx.doi.org/10.1016/j.plasmid.2013.03.004
URIhttp://hdl.handle.net/10261/88209
DOI10.1016/j.plasmid.2013.03.004
Identifiersdoi: 10.1016/j.plasmid.2013.03.004
issn: 0147-619X
e-issn: 1095-9890
Appears in Collections:(IBMB) Artículos
(CIB) Artículos
Files in This Item:
File Description SizeFormat 
nicking_activity _Fernandez.pdf578,62 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.