Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 Jul 11:4:45.
doi: 10.3389/fmolb.2017.00045. eCollection 2017.

Probing Long Non-coding RNA-Protein Interactions

Affiliations
Review

Probing Long Non-coding RNA-Protein Interactions

Jasmine Barra et al. Front Mol Biosci. .

Abstract

Non-coding RNA sequences outnumber the protein-coding genes in the human genome, however our knowledge of their functions is still limited. RNA-binding proteins follow the transcripts, including non-coding RNAs, throughout their life, regulating not only maturation, nuclear export, stability and eventually translation, but also RNA functions. Therefore, development of sophisticated methods to study RNA-protein interactions are key to the systematic characterization of lncRNAs. Although mostly applicable to RNA-protein interactions in general, many approaches, especially the computational ones, need adjustment to be adapted to the length and complexity of lncRNA transcripts. Here we critically review all the wet lab and computational methods to study lncRNA-protein interactions and their potential to clarify the dark side of the genome.

Keywords: RBPs; RNA; RNA immunoprecipitation; crosslinking; pull-down assays.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Workflow for the identification of RNA-protein interactions.

References

    1. Adriaens C., Standaert L., Barra J., Latil M., Verfaillie A., Kalev P., et al. . (2016). p53 induces formation of NEAT1 lncRNA-containing paraspeckles that modulate replication stress response and chemosensitivity. Nat. Med. 22, 861–868. 10.1038/nm.4135 - DOI - PubMed
    1. Arun G., Diermeier S., Akerman M., Chang K. C., Wilkinson J. E., Hearn S., et al. . (2016). Differentiation of mammary tumors and reduction in metastasis upon Malat1 lncRNA loss. Genes Dev. 30, 34–51. 10.1101/gad.270959.115 - DOI - PMC - PubMed
    1. Ascano M., Hafner M., Cekan P., Gerstberger S., Tuschl T. (2012). Identification of RNA-protein interaction networks using PAR-CLIP. Wiley Interdiscipl. Rev. RNA. 3, 159–177. 10.1002/wrna.1103 - DOI - PMC - PubMed
    1. Baltz A. G., Munschauer M., Schwanhäusser B., Vasile A., Murakawa Y., Schueler M., et al. . (2012). The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts. Mol. Cell 46, 674–690. 10.1016/j.molcel.2012.05.021 - DOI - PubMed
    1. Bell T. J., Eiríksdóttir E., Langel Ü., Eberwine J. (2011). Cell-Penetrating Peptides 683, 473–486. 10.1007/978-1-60761-919-2_34 - DOI - PubMed

LinkOut - more resources