Selenocysteine tRNA methylation promotes oxidative stress resistance in melanoma metastasis

Abstract

AbstractSelenocysteine-containing proteins play a central role in redox homeostasis. Their translation is a highly regulated process dependent on two tRNASecisodecoders differing by a single 2’-O-ribose methylation, called Um34. We characterized FTSJ1 as the Um34 methyltransferase and show that its activity is required for efficient selenocysteine insertion at the UGA stop codon during translation. Specifically, Loss of Um34 leads to ribosomal stalling and decreased UGA recoding. FTSJ1-deficient cells are more sensitive to oxidative stress and have decreased metastatic colonization in xenograft models of melanoma metastasis. Our findings uncover a role for tRNASecUm34 modification in oxidative stress resistance and highlight FTSJ1 as a potential therapeutic target specific for metastatic disease.