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Global analysis of the RNA-protein interaction and RNA secondary structure landscapes of the Arabidopsis nucleus.
Gosai, Sager J; Foley, Shawn W; Wang, Dongxue; Silverman, Ian M; Selamoglu, Nur; Nelson, Andrew D L; Beilstein, Mark A; Daldal, Fevzi; Deal, Roger B; Gregory, Brian D.
Afiliación
  • Gosai SJ; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Foley SW; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA; Cell and Molecular Biology Graduate Group, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Wang D; Department of Biology, Emory University, Atlanta, GA 30322, USA.
  • Silverman IM; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA; Cell and Molecular Biology Graduate Group, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Selamoglu N; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Nelson AD; School of Plant Sciences, University of Arizona, Tucson, AZ 85721, USA.
  • Beilstein MA; School of Plant Sciences, University of Arizona, Tucson, AZ 85721, USA.
  • Daldal F; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Deal RB; Department of Biology, Emory University, Atlanta, GA 30322, USA.
  • Gregory BD; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA; Cell and Molecular Biology Graduate Group, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: bdgregor@sas.upenn.edu.
Mol Cell ; 57(2): 376-88, 2015 Jan 22.
Article en En | MEDLINE | ID: mdl-25557549
ABSTRACT
Posttranscriptional regulation in eukaryotes requires cis- and trans-acting features and factors including RNA secondary structure and RNA-binding proteins (RBPs). However, a comprehensive view of the structural and RBP interaction landscape of nuclear RNAs has yet to be compiled for any organism. Here, we use our ribonuclease-mediated structure and RBP-binding site mapping approaches to globally profile these features in Arabidopsis seedling nuclei in vivo. We reveal anticorrelated patterns of secondary structure and RBP binding throughout nuclear mRNAs that demarcate sites of alternative splicing and polyadenylation. We also uncover a collection of protein-bound sequence motifs, and identify their structural contexts, co-occurrences in transcripts encoding functionally related proteins, and interactions with putative RBPs. Finally, using these motifs, we find that the chloroplast RBP CP29A also interacts with nuclear mRNAs. In total, we provide a simultaneous view of the RNA secondary structure and RBP interaction landscapes in a eukaryotic nucleus.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ribonucleoproteínas / ARN Mensajero / Núcleo Celular / Arabidopsis / ARN de Planta / Proteínas de Arabidopsis / Proteínas de Cloroplastos Tipo de estudio: Prognostic_studies Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ribonucleoproteínas / ARN Mensajero / Núcleo Celular / Arabidopsis / ARN de Planta / Proteínas de Arabidopsis / Proteínas de Cloroplastos Tipo de estudio: Prognostic_studies Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos