Translational control of methionine and serine metabolic pathways underpin the paralog-specific phenotypes of Rpl22 ribosomal protein mutants in cell division and replicative longevity
Nairita Maitra, Chong Z. He, Heidi M. Blank, Mitsuhiro Tsuchiya, Birgit Schilling, Matt R. Kaeberlein, Rodolfo Aramayo, Brian Keith Kennedy, Michael Polymenis
The paper identifies translational control of methionine and serine metabolic pathways as the mechanism underlying paralog-specific phenotypes in Rpl22 ribosomal protein mutants, linking these changes to cell division and replicative longevity.
bioRxiv · Feb 5, 2020 · PreprintMolecular Biology