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Mapping protein-RNA binding in plants with individual-nucleotide-resolution UV cross-linking and immunoprecipitation (plant iCLIP2).
Lewinski, Martin; Brüggemann, Mirko; Köster, Tino; Reichel, Marlene; Bergelt, Thorsten; Meyer, Katja; König, Julian; Zarnack, Kathi; Staiger, Dorothee.
Affiliation
  • Lewinski M; RNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, Germany.
  • Brüggemann M; Buchmann Institute for Molecular Life Sciences (BMLS) & Institute of Molecular Biosciences, Goethe University Frankfurt, Frankfurt, Germany.
  • Köster T; RNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, Germany.
  • Reichel M; RNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, Germany.
  • Bergelt T; RNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, Germany.
  • Meyer K; RNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, Germany.
  • König J; Institute of Molecular Biology (IMB), Mainz, Germany.
  • Zarnack K; Buchmann Institute for Molecular Life Sciences (BMLS) & Institute of Molecular Biosciences, Goethe University Frankfurt, Frankfurt, Germany.
  • Staiger D; RNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, Germany. dorothee.staiger@uni-bielefeld.de.
Nat Protoc ; 19(4): 1183-1234, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38278964
ABSTRACT
Despite crucial roles of RNA-binding proteins (RBPs) in plant physiology and development, methods for determining their transcriptome-wide binding landscape are less developed than those used in other model organisms. Cross-linking and immunoprecipitation (CLIP) methods (based on UV-mediated generation of covalent bonds between RNAs and cognate RBPs in vivo, purification of the cross-linked complexes and identification of the co-purified RNAs by high-throughput sequencing) have been applied mainly in mammalian cells growing in monolayers or in translucent tissue. We have developed plant iCLIP2, an efficient protocol for performing individual-nucleotide-resolution CLIP (iCLIP) in plants, tailored to overcome the experimental hurdles posed by plant tissue. We optimized the UV dosage to efficiently cross-link RNA and proteins in plants and expressed epitope-tagged RBPs under the control of their native promoters in loss-of-function mutants. We select epitopes for which nanobodies are available, allowing stringent conditions for immunopurification of the RNA-protein complexes to be established. To overcome the inherently high RNase content of plant cells, RNase inhibitors are added and the limited RNA fragmentation step is modified. We combine the optimized isolation of RBP-bound RNAs with iCLIP2, a streamlined protocol that greatly enhances the efficiency of library preparation for high-throughput sequencing. Plant researchers with experience in molecular biology and handling of RNA can complete this iCLIP2 protocol in ~5 d. Finally, we describe a bioinformatics workflow to determine targets of Arabidopsis RBPs from iCLIP data, covering all steps from downloading sequencing reads to identifying cross-linking events ( https//github.com/malewins/Plant-iCLIPseq ), and present the R/Bioconductor package BindingSiteFinder to extract reproducible binding sites ( https//bioconductor.org/packages/release/bioc/html/BindingSiteFinder.html ).
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA / Nucleotides Limits: Animals Language: En Journal: Nat Protoc / Nat. Protoc / Nature protocols Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA / Nucleotides Limits: Animals Language: En Journal: Nat Protoc / Nat. Protoc / Nature protocols Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido