Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/52685
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dc.contributor.authorBensaid, M.en
dc.contributor.authorMelko, M.en
dc.contributor.authorBechara, E.en
dc.contributor.authorDavidovic, L.en
dc.contributor.authorBerretta, A.en
dc.contributor.authorCatania, M.en
dc.contributor.authorGecz, J.en
dc.contributor.authorLalli, E.en
dc.contributor.authorBardoni, B.en
dc.date.issued2009en
dc.identifier.citationNucleic Acids Research, 2009; 37(4):1269-1279en
dc.identifier.issn0305-1048en
dc.identifier.issn1362-4962en
dc.identifier.urihttp://hdl.handle.net/2440/52685-
dc.description.abstractFRAXE is a form of mild to moderate mental retardation due to the silencing of the FMR2 gene. The cellular function of FMR2 protein is presently unknown. By analogy with its homologue AF4, FMR2 was supposed to have a role in transcriptional regulation, but robust evidences supporting this hypothesis are lacking. We observed that FMR2 co-localizes with the splicing factor SC35 in nuclear speckles, the nuclear regions where splicing factors are concentrated, assembled and modified. Similarly to what was reported for splicing factors, blocking splicing or transcription leads to the accumulation of FMR2 in enlarged, rounded speckles. FMR2 is also localized in the nucleolus when splicing is blocked. We show here that FMR2 is able to specifically bind the G-quartet-forming RNA structure with high affinity. Remarkably, in vivo, in the presence of FMR2, the ESE action of the G-quartet situated in mRNA of an alternatively spliced exon of a minigene or of the putative target FMR1 appears reduced. Interestingly, FMR1 is silenced in the fragile X syndrome, another form of mental retardation. All together, our findings strongly suggest that FMR2 is an RNA-binding protein, which might be involved in alternative splicing regulation through an interaction with G-quartet RNA structure.en
dc.description.statementofresponsibilityMounia Bensaid, Mireille Melko, Elias G. Bechara, Laetitia Davidovic, Antonio Berretta, Maria Vincenza Catania, Jozef Gecz, Enzo Lalli, and Barbara Bardonien
dc.language.isoenen
dc.publisherOxford Univ Pressen
dc.subjectCells, Cultured; Cell Line; Cell Nucleus Structures; Animals; Humans; Mice; RNA-Binding Proteins; Nuclear Proteins; RNA; Alternative Splicing; Protein Structure, Tertiary; Fragile X Mental Retardation Protein; G-Quadruplexesen
dc.titleFRAXE-associated mental retardation protein (FMR2) is an RNA-binding protein with high affinity for G-quartet RNA forming structureen
dc.typeJournal articleen
dc.identifier.rmid0020090274en
dc.identifier.doi10.1093/nar/gkn1058en
dc.identifier.pubid39225-
pubs.library.collectionPaediatrics publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]en
Appears in Collections:Paediatrics publications

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