Ribosomal RNA expansion segments mediate the oligomerization of inactive animal ribosomes
Summary
Cells down-regulate protein synthesis when stressed to conserve energy and shift resources toward repair. We found that in some mammalian cells, including neurons, stress also resulted in the formation of inactive ribosome-ribosome clusters (disomes). We used cryo-electron tomography (cryo-ET) to visualize ribosomes in situ and observed that this ribosome dimerization was mediated by a homotypic interaction of the ribosomal RNA (rRNA) expansion segment ES31Lb. ES31Lb interactions were both
Content
# Ribosomal RNA expansion segments mediate the oligomerization of inactive animal ribosomes
*Published: 2026 Feb 19*
Cells down-regulate protein synthesis when stressed to conserve energy and shift
resources toward repair. We found that in some mammalian cells, including
neurons, stress also resulted in the formation of inactive ribosome-ribosome
clusters (disomes). We used cryo-electron tomography (cryo-ET) to visualize
ribosomes in situ and observed that this ribosome dimerization was mediated by a
homotypic interaction of the ribosomal RNA (rRNA) expansion segment ES31Lb.
ES31Lb interactions were both necessary and sufficient for disome formation and
conferred a growth advantage and stress resistance to brain cells. ES31Lb is
predicted to homodimerize in ~20% of chordates, including variants in both
chicken and human. Cryo-ET analysis of chicken tetrasomes revealed an
interaction between ES31Lb and ES9La. Thus, in animal cells, translation
regulation can use a flexible component of the protein synthesis machinery-rRNA
expansion segments.
DOI: 10.1126/science.adr4287