4) Germ granule mRNAs are replete with GC-rich complementary sequences predicted to be competent of engaging in persistent intermolecular base pairing however in vivo these interactions are unrealized and restricted by RNA folding.

3) Engineered germ granule mRNAs with exposed GC-rich complementary sequences (CSs) within stem loops induce sustained base pairing in vitro and enhanced intermolecular interactions in vivo. But, the presence of these structures disrupts development, and GC-rich CSs exacerbate this phenotype.

We find that:
1) mRNAs remain structured within germ granules
2) mRNAs base pair intermolecularly without high sequence complementarity or significant melting of secondary structure. Base pairing is driven by scattered and discontinuous stretches of bases appearing on the surface of structured RNAs

Jeffery is presenting his work at the annual RNA society meeting in San Diego - visit his poster! #RNA25; #RNA2025

Jeffery is presenting his work at the annual RNA society meeting in San Diego - visit his poster! #RNA25; #RNA2025

We propose that the combined suppression of intermolecular base pairing and the increased RNA structural diversity may serve as a mechanism to preserve normal RNA function during stress, while also facilitating the reversible assembly of stress granules

c) However, these RNAs increase in structural diversity in a manner dependent on oxidative stress and the stress granule nucleating proteins G3BP1 and G3BP2.
d) In the absence of the main stress granule nucleating proteins G3BP1 and G3BP2, mRNAs remain dispersed in cells during oxidative stress

We show that:
a) Oxidative stress downregulates intermolecular base pairing of reporter mRNAs engineered to enhance detection of such interactions.
b) RNA regions within transcripts that enrich in stress granules remain structured during stress.