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Mol Cell ; 57(3): 397-407, 2015 Feb 05.
Artigo em Inglês | MEDLINE | ID: mdl-25557550

RESUMO

RNA-mediated gene silencing in human cells requires the accurate generation of ∼22 nt microRNAs (miRNAs) from double-stranded RNA substrates by the endonuclease Dicer. Although the phylogenetically conserved RNA-binding proteins TRBP and PACT are known to contribute to this process, their mode of Dicer binding and their genome-wide effects on miRNA processing have not been determined. We solved the crystal structure of the human Dicer-TRBP interface, revealing the structural basis of the interaction. Interface residues conserved between TRBP and PACT show that the proteins bind to Dicer in a similar manner and by mutual exclusion. Based on the structure, a catalytically active Dicer that cannot bind TRBP or PACT was designed and introduced into Dicer-deficient mammalian cells, revealing selective defects in guide strand selection. These results demonstrate the role of Dicer-associated RNA binding proteins in maintenance of gene silencing fidelity.


Assuntos
RNA Helicases DEAD-box/química , RNA Helicases DEAD-box/metabolismo , MicroRNAs/metabolismo , Proteínas de Ligação a RNA/química , Proteínas de Ligação a RNA/metabolismo , Ribonuclease III/metabolismo , Animais , Proteínas Argonautas/metabolismo , Domínio Catalítico , Células Cultivadas , Cristalografia por Raios X , RNA Helicases DEAD-box/genética , Inativação Gênica , Humanos , Camundongos , Dados de Sequência Molecular , Conformação Proteica , Ribonuclease III/química , Alinhamento de Sequência
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