Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/376
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dc.contributor.authorRodić, Anđelaen_US
dc.contributor.authorBlagojevic, Bojanaen_US
dc.contributor.authorZdobnov, Evgenyen_US
dc.contributor.authorDjordjevic, Magdalenaen_US
dc.contributor.authorĐorđević, Markoen_US
dc.date.accessioned2019-07-01T14:08:16Z-
dc.date.available2019-07-01T14:08:16Z-
dc.date.issued2017-02-24-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/376-
dc.description.abstract© 2017 The Author(s). Background: Restriction-modification (R-M) systems are rudimentary bacterial immune systems. The main components include restriction enzyme (R), which cuts specific unmethylated DNA sequences, and the methyltransferase (M), which protects the same DNA sequences. The expression of R-M system components is considered to be tightly regulated, to ensure successful establishment in a naïve bacterial host. R-M systems are organized in different architectures (convergent or divergent) and are characterized by different features, i.e. binding cooperativities, dissociation constants of dimerization, translation rates, which ensure this tight regulation. It has been proposed that R-M systems should exhibit certain dynamical properties during the system establishment, such as: i) a delayed expression of R with respect to M, ii) fast transition of R from "OFF" to "ON" state, iii) increased stability of the toxic molecule (R) steady-state levels. It is however unclear how different R-M system features and architectures ensure these dynamical properties, particularly since it is hard to address this question experimentally. Results: To understand design of different R-M systems, we computationally analyze two R-M systems, representative of the subset controlled by small regulators called 'C proteins', and differing in having convergent or divergent promoter architecture. We show that, in the convergent system, abolishing any of the characteristic system features adversely affects the dynamical properties outlined above. Moreover, an extreme binding cooperativity, accompanied by a very high dissociation constant of dimerization, observed in the convergent system, but absent from other R-M systems, can be explained in terms of the same properties. Furthermore, we develop the first theoretical model for dynamics of a divergent R-M system, which does not share any of the convergent system features, but has overlapping promoters. We show that i) the system dynamics exhibits the same three dynamical properties, ii) introducing any of the convergent system features to the divergent system actually diminishes these properties. Conclusions: Our results suggest that different R-M architectures and features may be understood in terms of constraints imposed by few simple dynamical properties of the system, providing a unifying framework for understanding these seemingly diverse systems. We also provided predictions for the perturbed R-M systems dynamics, which may in future be tested through increasingly available experimental techniques, such as re-engineering R-M systems and single-cell experiments.en_US
dc.language.isoenen_US
dc.relation.ispartofBMC Systems Biologyen_US
dc.subjectBacterial immune systemsen_US
dc.subjectBiophysical modelingen_US
dc.subjectGene expression dynamicsen_US
dc.subjectRestriction-modificationen_US
dc.subjectTranscription regulationen_US
dc.titleUnderstanding key features of bacterial restriction-modification systems through quantitative modelingen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s12918-016-0377-x-
dc.identifier.pmid28466789-
dc.identifier.scopus2-s2.0-85013823018-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85013823018-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.orcid0000-0003-2872-9066-
crisitem.author.orcid0000-0002-2903-3119-
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