| Literature DB >> 32817343 |
Santi Mestre-Fos1,2,3, Chieri Ito1,2,3, Courtney M Moore2,3, Amit R Reddi4,3,5, Loren Dean Williams6,2,3,5.
Abstract
The in vitro formation of stable G-quadruplexes (G4s) in human rRNA was recently reported. However, their formation in cells and their cellular roles were not resolved. Here, by taking a chemical biology approach that integrates results from immunofluorescence, G4 ligands, heme-affinity reagents, and a genetically encoded fluorescent heme sensor, we report that human ribosomes can form G4s in vivo that regulate heme bioavailability. Immunofluorescence experiments indicate that the vast majority of extra-nuclear G4s are associated with rRNA. Moreover, titrating human cells with a G4 ligand alters the ability of ribosomes to bind heme and disrupts cellular heme bioavailability as measured by a genetically encoded fluorescent heme sensor. Overall, these results suggest that ribosomes play a role in regulating heme homeostasis.Entities:
Keywords: BG4; G-quadruplex; G-tract; G4; RNA; expansion segments; heme; hemin; metal homeostasis; ribosomal ribonucleic acid (rRNA) (ribosomal RNA); ribosome; tentacle
Year: 2020 PMID: 32817343 PMCID: PMC7606673 DOI: 10.1074/jbc.RA120.014332
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157