| Literature DB >> 28380354 |
Joel V Tamayo1, Takamasa Teramoto2, Seema Chatterjee1, Traci M Tanaka Hall3, Elizabeth R Gavis4.
Abstract
The Drosophila hnRNP F/H homolog, Glorund (Glo), regulates nanos mRNA translation by interacting with a structured UA-rich motif in the nanos 3' untranslated region. Glo regulates additional RNAs, however, and mammalian homologs bind G-tract sequences to regulate alternative splicing, suggesting that Glo also recognizes G-tract RNA. To gain insight into how Glo recognizes both structured UA-rich and G-tract RNAs, we used mutational analysis guided by crystal structures of Glo's RNA-binding domains and identified two discrete RNA-binding surfaces that allow Glo to recognize both RNA motifs. By engineering Glo variants that favor a single RNA-binding mode, we show that a subset of Glo's functions in vivo is mediated solely by the G-tract binding mode, whereas regulation of nanos requires both recognition modes. Our findings suggest a molecular mechanism for the evolution of dual RNA motif recognition in Glo that may be applied to understanding the functional diversity of other RNA-binding proteins.Entities:
Keywords: Drosophila; Glorund; RNA-binding protein; development; hnRNP; hnRNP F; hnRNP H; nanos; post-transcriptional regulation; translational control; translational repressor
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Year: 2017 PMID: 28380354 PMCID: PMC5392723 DOI: 10.1016/j.celrep.2017.03.022
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423