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dc.contributor.authorBosse, Gabriel D.
dc.contributor.authorRuegger, Stefan
dc.contributor.authorOw, Maria C.
dc.contributor.authorVasquez-Rifo, Alejandro
dc.contributor.authorRondeau, Evelyne L.
dc.contributor.authorAmbros, Victor R.
dc.contributor.authorGrosshans, Helge
dc.contributor.authorSimard, Martin J.
dc.date2022-08-11T08:10:18.000
dc.date.accessioned2022-08-23T17:03:28Z
dc.date.available2022-08-23T17:03:28Z
dc.date.issued2013-04-25
dc.date.submitted2015-01-12
dc.identifier.citationMol Cell. 2013 Apr 25;50(2):281-7. doi: 10.1016/j.molcel.2013.02.023. Epub 2013 Mar 28. <a href="http://dx.doi.org/10.1016/j.molcel.2013.02.023">Link to article on publisher's site</a>
dc.identifier.issn1097-2765 (Linking)
dc.identifier.doi10.1016/j.molcel.2013.02.023
dc.identifier.pmid23541767
dc.identifier.urihttp://hdl.handle.net/20.500.14038/44432
dc.description.abstractIn metazoans, microRNAs play a critical role in the posttranscriptional regulation of genes required for cell proliferation and differentiation. MicroRNAs themselves are regulated by a multitude of mechanisms influencing their transcription and posttranscriptional maturation. However, there is only sparse knowledge on pathways regulating the mature, functional form of microRNA. Here, we uncover the implication of the decapping scavenger protein DCS-1 in the control of microRNA turnover. In Caenorhabditis elegans, mutations in dcs-1 increase the levels of functional microRNAs. We demonstrate that DCS-1 interacts with the exonuclease XRN-1 to promote microRNA degradation in an independent manner from its known decapping scavenger activity, establishing two molecular functions for DCS-1. Our findings thus indicate that DCS-1 is part of a degradation complex that performs microRNA turnover in animals.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23541767&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.molcel.2013.02.023
dc.subjectAnimals
dc.subjectCaenorhabditis elegans
dc.subjectCaenorhabditis elegans Proteins
dc.subjectExoribonucleases
dc.subjectGene Expression
dc.subjectMicroRNAs
dc.subjectMutation
dc.subjectN-Glycosyl Hydrolases
dc.subjectRNA Interference
dc.subjectRNA Stability
dc.subjectRNA, Helminth
dc.subjectRNA-Induced Silencing Complex
dc.subjectBiochemistry
dc.subjectMolecular Biology
dc.subjectMolecular Genetics
dc.titleThe decapping scavenger enzyme DCS-1 controls microRNA levels in Caenorhabditis elegans
dc.typeJournal Article
dc.source.journaltitleMolecular cell
dc.source.volume50
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pmm_pp/24
dc.identifier.contextkey6519776
html.description.abstract<p>In metazoans, microRNAs play a critical role in the posttranscriptional regulation of genes required for cell proliferation and differentiation. MicroRNAs themselves are regulated by a multitude of mechanisms influencing their transcription and posttranscriptional maturation. However, there is only sparse knowledge on pathways regulating the mature, functional form of microRNA. Here, we uncover the implication of the decapping scavenger protein DCS-1 in the control of microRNA turnover. In Caenorhabditis elegans, mutations in dcs-1 increase the levels of functional microRNAs. We demonstrate that DCS-1 interacts with the exonuclease XRN-1 to promote microRNA degradation in an independent manner from its known decapping scavenger activity, establishing two molecular functions for DCS-1. Our findings thus indicate that DCS-1 is part of a degradation complex that performs microRNA turnover in animals.</p>
dc.identifier.submissionpathpmm_pp/24
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages281-7


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