A novel gene-diet interaction promotes organismal lifespan and host protection during infection via the mitochondrial UPR

Abstract

Cells use a variety of mechanisms to maintain optimal mitochondrial function including the mitochondrial unfolded protein response (UPRmt). The UPRmtmitigates mitochondrial dysfunction by differentially regulating mitoprotective gene expression through the transcription factor ATFS-1. Since UPRmtactivation is commensurate with organismal benefits such as extended lifespan and host protection during infection, we sought to identify pathways that promote its stimulation. Using unbiased forward genetics screening, we isolated novel mutant alleles that could activate the UPRmt. Interestingly, we identified one reduction of function mutant allele (osa3) in the mitochondrial ribosomal genemrpl-2that activated the UPRmtin a diet-dependent manner. We find thatmrpl-2(osa3)mutants lived longer and survived better during pathogen infection depending on the diet they were fed. A diet containing low levels of vitamin B12 could activate the UPRmtinmrpl-2(osa3)animals. Also, we find that the vitamin B12-dependent enzyme methionine synthase intersects withmrpl-2(osa3)to activate the UPRmtand confer animal lifespan extension at the level of ATFS-1. Thus, we present a novel gene-diet pairing that promotes animal longevity that is mediated by the UPRmt.