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An architectural role of specific RNA-RNA interactions in oskar granules

Affiliations
  • 1Developmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
  • 2Department of Bioscience and Biotechnology, Indian Institute of Technology, Kharagpur, India.
  • 3Laboratory of Molecular Neuroscience, German Center for Neurodegenerative Diseases, Berlin, Germany.
  • 4Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany. julia.mahamid@embl.de.
  • 5Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, Germany. julia.mahamid@embl.de.
  • 6Developmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany. anne.ephrussi@embl.org.

Published on:

October 1, 2024

Abstract

Ribonucleoprotein (RNP) granules are membraneless condensates that organize the intracellular space by compartmentalization of specific RNAs and proteins. Studies have shown that RNA tunes the phase behaviour of RNA-binding proteins, but the role of intermolecular RNA-RNA interactions in RNP granules in vivo remains less explored. Here we determine the role of a sequence-specific RNA-RNA kissing-loop interaction in assembly of mesoscale oskar RNP granules in the female Drosophila germline. We show that a two-nucleotide mutation that disrupts kissing-loop-mediated oskar messenger RNA dimerization impairs condensate formation in vitro and oskar granule assembly in the developing oocyte, leading to defective posterior localization of the RNA and abrogation of oskar-associated processing bodies upon nutritional stress. This specific trans RNA-RNA interaction acts synergistically with the scaffold RNA-binding protein, Bruno, in driving condensate assembly. Our study highlights the architectural contribution of an mRNA and its specific secondary structure and tertiary interactions to the formation of an RNP granule that is essential for embryonic development.

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