Author: Martone, Julie; Mariani, Davide; Santini, Tiziana; Setti, Adriano; Shamloo, Sama; Colantoni, Alessio; Capparelli, Francesca; Paiardini, Alessandro; Dimartino, Dacia; Morlando, Mariangela; Bozzoni, Irene
Title: SMaRT lncRNA controls translation of a Gâ€quadruplexâ€containing mRNA antagonizing the DHX36 helicase Cord-id: lddewr9z Document date: 2020_4_26
ID: lddewr9z
Snippet: Guanineâ€quadruplexes (G4) included in RNA molecules exert several functions in controlling gene expression at postâ€transcriptional level; however, the molecular mechanisms of G4â€mediated regulation are still poorly understood. Here, we describe a regulatory circuitry operating in the early phases of murine muscle differentiation in which a long nonâ€coding RNA (SMaRT) base pairs with a G4â€containing mRNA (Mlxâ€Î³) and represses its translation by counteracting the activity of the DHX36
Document: Guanineâ€quadruplexes (G4) included in RNA molecules exert several functions in controlling gene expression at postâ€transcriptional level; however, the molecular mechanisms of G4â€mediated regulation are still poorly understood. Here, we describe a regulatory circuitry operating in the early phases of murine muscle differentiation in which a long nonâ€coding RNA (SMaRT) base pairs with a G4â€containing mRNA (Mlxâ€Î³) and represses its translation by counteracting the activity of the DHX36 RNA helicase. The timeâ€restricted, specific effect of lncâ€SMaRT on the translation of Mlxâ€Î³ isoform modulates the general subcellular localization of total MLX proteins, impacting on their transcriptional output and promoting proper myogenesis and mature myotube formation. Therefore, the circuitry made of lncâ€SMaRT, Mlxâ€Î³, and DHX36 not only plays an important role in the control of myogenesis but also unravels a molecular mechanism where G4 structures and G4 unwinding activities are regulated in living cells.
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