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Global Analysis of the RNA-Protein Interaction and RNA Secondary Structure Landscapes of the Arabidopsis Nucleus
- Source :
- Molecular Cell. 57(2):376-388
- Publication Year :
- 2015
- Publisher :
- Elsevier BV, 2015.
-
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.
- Subjects :
- endocrine system
Polyadenylation
Arabidopsis
RNA-binding protein
Computational biology
Biology
Article
Nucleic acid secondary structure
Chloroplast Proteins
RNA-Protein Interaction
Gene Expression Regulation, Plant
Consensus Sequence
medicine
RNA, Messenger
Molecular Biology
Ribonucleoprotein
Genetics
Cell Nucleus
Binding Sites
Base Sequence
Arabidopsis Proteins
Alternative splicing
RNA
Cell Biology
Cell nucleus
Protein Transport
medicine.anatomical_structure
Ribonucleoproteins
RNA, Plant
Seedlings
Nucleic Acid Conformation
RNA Interference
Transcriptome
Protein Binding
Subjects
Details
- ISSN :
- 10972765
- Volume :
- 57
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Molecular Cell
- Accession number :
- edsair.doi.dedup.....0e1897a8e8f05d6a5bf72fa965777d97
- Full Text :
- https://doi.org/10.1016/j.molcel.2014.12.004