Structural basis of phosphorylation-independent nuclear import of CIRBP by TNPO3

Transportin 3 (TNPO3) is a nuclear import receptor known for its broad substrate specificity, often recognizing arginine-serine (SR/RS) repeat-rich nuclear localization signals (NLS) in SRSF proteins. While serine phosphorylation or glutamate presence has been associated with these NLSs, recent proteomic studies identified TNPO3 cargoes lacking SR/RS repeats. One such example is the cold-inducible RNA-binding protein (CIRBP), which contains a non-classical RSY-NLS. Using X-ray crystallography, here we investigate the TNPO3-CIRBP interaction and find that tyrosines within the RSY-NLS play a key role in binding, independent of phosphorylation. Surprisingly, serine and tyrosine phosphorylation in CIRBP's NLS inhibits TNPO3 binding, suggesting a regulatory mechanism for nuclear import. Our study reveals a non-conventional nuclear import mechanism mediated by TNPO3, which may extend to other known or yet undiscovered TNPO3 cargoes.

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Publication Details

Journal
Nature Communications
Published
2025-05-14
DOI
https://doi.org/10.1038/s41467-025-59802-2
Citations
1
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
0.81

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article

Structural basis of phosphorylation-independent nuclear import of CIRBP by TNPO3

Benjamin Bourgeois, Saskia Hutten, Qishun Zhou, Tea Pavkov‐Keller et al.
1 citations
Nature Communications
RNA Research and Splicing
0.81
article

Structural basis of phosphorylation-independent nuclear import of CIRBP by TNPO3

Benjamin Bourgeois, Saskia Hutten, Qishun Zhou, Tea Pavkov‐Keller, Tobias Madl, Dorothee Dormann, Theo Sagmeister
article en
1 citations

Abstract

Transportin 3 (TNPO3) is a nuclear import receptor known for its broad substrate specificity, often recognizing arginine-serine (SR/RS) repeat-rich nuclear localization signals (NLS) in SRSF proteins. While serine phosphorylation or glutamate presence has been associated with these NLSs, recent proteomic studies identified TNPO3 cargoes lacking SR/RS repeats. One such example is the cold-inducible RNA-binding protein (CIRBP), which contains a non-classical RSY-NLS. Using X-ray crystallography, here we investigate the TNPO3-CIRBP interaction and find that tyrosines within the RSY-NLS play a key role in binding, independent of phosphorylation. Surprisingly, serine and tyrosine phosphorylation in CIRBP's NLS inhibits TNPO3 binding, suggesting a regulatory mechanism for nuclear import. Our study reveals a non-conventional nuclear import mechanism mediated by TNPO3, which may extend to other known or yet undiscovered TNPO3 cargoes.

Nature CommunicationsVol. 16(1)
Centre National de la Recherche Scientifique (FR), Institut Pasteur (FR), University of Graz (AT), Johannes Gutenberg University Mainz (DE), Medical University of Graz (AT), Université Paris Cité (FR), BioTechMed-Graz (AT), Institute of Molecular Biology (DE)
European Commission, Deutsche Forschungsgemeinschaft, Austrian Science Fund, Österreichische Forschungsförderungsgesellschaft, Karl-Franzens-Universität Graz, Medizinische Universität Graz, BioTechMed-Graz, European Regional Development Fund
Openalex Percentile: Top 28%
RNA Research and Splicing
0.81
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