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               <dc:title>The Microprocessor controls the activity of mammalian retrotransposons</dc:title>
               <dc:creator>Heras, Sara R.</dc:creator>
               <dc:creator>Macias, Sara</dc:creator>
               <dc:creator>Plass Pórtulas, Mireya, 1982-</dc:creator>
               <dc:creator>Fernandez, Noemí</dc:creator>
               <dc:creator>Cano Ferrer, David</dc:creator>
               <dc:creator>Eyras Jiménez, Eduardo</dc:creator>
               <dc:creator>Garcia Perez, José L.</dc:creator>
               <dc:creator>Cáceres, Javier F.</dc:creator>
               <dc:subject>miRNAs</dc:subject>
               <dc:subject>RNA</dc:subject>
               <dc:subject>Transposition</dc:subject>
               <dc:description>More than half of the human genome is made of transposable elements whose ongoing mobilization is a driving force in genetic diversity; however, little is known about how the host regulates their activity. Here, we show that the Microprocessor (Drosha-DGCR8), which is required for microRNA biogenesis, also recognizes and binds RNAs derived from human long interspersed element 1 (LINE-1), Alu and SVA retrotransposons. Expression analyses demonstrate that cells lacking a functional Microprocessor accumulate LINE-1 mRNA and encoded proteins. Furthermore, we show that structured regions of the LINE-1 mRNA can be cleaved in vitro by Drosha. Additionally, we used a cell culture–based assay to show that the Microprocessor negatively regulates LINE-1 and Alu retrotransposition in vivo. Altogether, these data reveal a new role for the Microprocessor as a post-transcriptional repressor of mammalian retrotransposons and a defender of human genome integrity.</dc:description>
               <dc:description>S.R.H. was supported by a Marie Curie Intra-European Fellowship and a Marie Curie CIG-Grant (PCIG10-GA-2011-303812). M.P. and E.E. were supported by the Spanish Ministry of Science (BIO2011-23920) and by the Sandra Ibarra Foundation (CSD2009-00080). M.P. is supported by the Novo Nordisk Foundation. J.L.G.-P. is supported by FP7-PEOPLE-2007-4-3-IRG, CICE-FEDER-P09-CTS-4980, PeS-FEDER-PI-002, FIS-FEDER-PI11/01489 and the Howard Hughes Medical Institute (IECS-55007420). J.F.C. was supported by Core funding from the Medical Research Council and by the Wellcome Trust (grant 095518/B/11/Z).</dc:description>
               <dc:date>2019-02-04T15:26:58Z</dc:date>
               <dc:date>2019-02-04T15:26:58Z</dc:date>
               <dc:date>2013</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:relation>Nature Structural &amp;amp; Molecular Biology. 2013;20(10):1173-81</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/ES/3PN/BIO2011-23920</dc:relation>
               <dc:rights>© Springer Nature Publishing AG. Heras SR, Macias S, Plass M, Fernandez N, Cano D, Eyras E, Garcia-Perez JL, Cáceres JF. The Microprocessor controls the activity of mammalian retrotransposons. Nat Struct Mol Biol. 2013; 20(10):1173-81. DOI 10.1038/nsmb.2658 [http://dx.doi.org/10.1038/nsmb.2658]</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Nature Research</dc:publisher>
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