Project Details
Projekt Print View

Understanding the link between splicing and mRNA localization by structural biology

Subject Area Structural Biology
Term from 2017 to 2022
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 355518810
 
Final Report Year 2024

Final Report Abstract

The discovery of several functional interactions where one or even both partners remain disordered has demonstrated that specific interactions do not necessarily require well-defined intermolecular interfaces. Here, using a combination of NMR spectroscopy and EMSAs, we have characterized a fuzzy protein–RNA complex formed by the intrinsically unfolded protein PYM and RNA. PYM is a cytosolic protein, which has been reported to bind the exon junction complex (EJC). In the process of oskar mRNA localization in Drosophila melanogaster, splicing of the first intron and deposition of the EJC are essential, while PYM is required to recycle the EJC components after localization has been accomplished. Here we demonstrated that the first 160 amino acids of PYM (PYM1–160) are intrinsically disordered. PYM1–160 binds RNA independently of its nucleotide sequence, forming a fuzzy protein–RNA complex which does not contain well-structured protein–RNA interfaces. The driving force for the interaction is charge complementarity, together with preservation of conformational entropy. Formation of this complex is incompatible with PYM’s binding to the EJC recycling factor. We propose that the role of RNA binding consists in down-regulating PYM activity by blocking the EJC interaction surface of PYM until localization has been accomplished. At the same time, the interaction of PYM with the RNA may contribute to ensure that PYM is localized together with the mRNA and the EJC. We suggest that the largely unstructured character of PYM may act to enable binding to a variety of diverse interaction partners, such as multiple RNA sequences and the EJC proteins Y14 and Mago. We propose that functional, fuzzy interactions between charged molecules may be much more common than previously thought. The less well-defined energy landscape underlying such interactions may allow the participants to fulfil multiple roles in different cellular pathways.

Publications

 
 

Additional Information

Textvergrößerung und Kontrastanpassung