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dc.contributor.authorClingman, Carina C.
dc.contributor.authorRyder, Sean P.
dc.date2022-08-11T08:08:29.000
dc.date.accessioned2022-08-23T15:56:49Z
dc.date.available2022-08-23T15:56:49Z
dc.date.issued2013-07-01
dc.date.submitted2013-06-05
dc.identifier.citationClingman, C. C. and Ryder, S. P. (2013), Metabolite sensing in eukaryotic mRNA biology. WIREs RNA, 4(4):387–396. doi: 10.1002/wrna.1167. <a href="http://dx.doi.org/10.1002/wrna.1167">Link to article on publisher's site</a>
dc.identifier.issn1757-7004 (Linking)
dc.identifier.doi10.1002/wrna.1167
dc.identifier.pmid23653333
dc.identifier.urihttp://hdl.handle.net/20.500.14038/30055
dc.description.abstractAll living creatures change their gene expression program in response to nutrient availability and metabolic demands. Nutrients and metabolites can directly control transcription and activate second-messenger systems. More recent studies reveal that metabolites also affect post-transcriptional regulatory mechanisms. Here, we review the increasing number of connections between metabolism and post-transcriptional regulation in eukaryotic organisms. First, we present evidence that riboswitches, a common mechanism of metabolite sensing in bacteria, also function in eukaryotes. Next, we review an example of a double stranded RNA modifying enzyme that directly interacts with a metabolite, suggesting a link between RNA editing and metabolic state. Finally, we discuss work that shows some metabolic enzymes bind directly to RNA to affect mRNA stability or translation efficiency. These examples were discovered through gene-specific genetic, biochemical, and structural studies. A directed systems level approach will be necessary to determine whether they are anomalies of evolution or pioneer discoveries in what may be a broadly connected network of metabolism and post-transcriptional regulation. WIREs RNA 2013. doi: 10.1002/wrna.1167 For further resources related to this article, please visit the WIREs website.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23653333&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1002/wrna.1167
dc.subjectEukaryota
dc.subjectMetabolism
dc.subjectRiboswitch
dc.subjectRNA, Messenger
dc.subjectBiochemistry, Biophysics, and Structural Biology
dc.subjectGenetics and Genomics
dc.titleMetabolite sensing in eukaryotic mRNA biology
dc.typeJournal Article
dc.source.journaltitleWiley interdisciplinary reviews. RNA
dc.source.volume4
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/29
dc.identifier.contextkey4199959
html.description.abstract<p>All living creatures change their gene expression program in response to nutrient availability and metabolic demands. Nutrients and metabolites can directly control transcription and activate second-messenger systems. More recent studies reveal that metabolites also affect post-transcriptional regulatory mechanisms. Here, we review the increasing number of connections between metabolism and post-transcriptional regulation in eukaryotic organisms. First, we present evidence that riboswitches, a common mechanism of metabolite sensing in bacteria, also function in eukaryotes. Next, we review an example of a double stranded RNA modifying enzyme that directly interacts with a metabolite, suggesting a link between RNA editing and metabolic state. Finally, we discuss work that shows some metabolic enzymes bind directly to RNA to affect mRNA stability or translation efficiency. These examples were discovered through gene-specific genetic, biochemical, and structural studies. A directed systems level approach will be necessary to determine whether they are anomalies of evolution or pioneer discoveries in what may be a broadly connected network of metabolism and post-transcriptional regulation. WIREs RNA 2013. doi: 10.1002/wrna.1167 For further resources related to this article, please visit the WIREs website.</p>
dc.identifier.submissionpathfaculty_pubs/29
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages387–396


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