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dc.contributor.authorMehdizadeh Aghdam, E
dc.contributor.authorHejazi, MS
dc.contributor.authorBarzegar, A
dc.date.accessioned2018-08-26T05:37:14Z
dc.date.available2018-08-26T05:37:14Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39810
dc.description.abstractRiboswitches are generally located in 5'-UTR region of mRNAs and specifically bind small ligands. Following ligand binding, gene expression is controlled mostly by transcription termination, translation inhibition or mRNA degradation processes. More than 30 classes of known riboswitches have been identified by now. Most riboswitches consist of an aptamer domain and an expression platform. The aptamer domain of each class of riboswitch is a conserved structure and stabilizes specific structures of the expression platforms through binding to specific compounds. In this review, we are highlighting most aspects of riboswitch research including the novel riboswitch discoveries, routine methods for discovering and investigating riboswitches along with newly discovered classes and mechanistic principles of riboswitch-mediated gene expression control. Moreover, we will give an overview about the potential of riboswitches as therapeutic targets for antibiotic design and also their utilization as biosensors for molecular detection.
dc.language.isoEnglish
dc.relation.ispartofGene
dc.subjectAnimals
dc.subjectAnti-Bacterial Agents
dc.subjectBiosensing Techniques
dc.subjectDrug Discovery
dc.subjectHumans
dc.subjectRiboswitch
dc.titleRiboswitches: From living biosensors to novel targets of antibiotics.
dc.typearticle
dc.citation.volume592
dc.citation.issue2
dc.citation.spage244
dc.citation.epage59
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1016/j.gene.2016.07.035


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