2Diseases that affect the mitochondrial electron transport chain (ETC) often manifest as threshold effect 2 3 disorders, meaning patients only become symptomatic once a certain level of ETC dysfunction is 2 4 reached. Multiple processes work to control proximity to the critical ETC threshold and as a 2 5 consequence there can be significant variability in disease presentation among patients. Identification 2 6 of such control processes remains an ongoing goal. Checkpoint signaling comprises a collection of alert 2 7 mechanisms activated in cells in response to nuclear DNA damage. Well-defined hierarchies of 2 8 proteins are involved in both sensing and signaling DNA damage, with ATM (ataxia telangiectasia 2 9 mutated) and ATR (ATM and Rad3-related) acting as pivotal signaling kinases. In the nematode 3 0 C. elegans, severe reduction of mitochondrial ETC activity shortens life, as in humans, but mild 3 1 2 reduction extends life as a consequence of survival strategies that are invoked under these 3 2 circumstances. Here we show that removal of ATL-1, the worm ortholog of ATR, unexpectedly lessens 3 3 the severity of ETC dysfunction, but removal of ATM does not. Multiple genetic and biochemical tests 3 4show no evidence for increased mutation or DNA breakage in animals exposed to ETC disruption.
5Instead, we find that reduced ETC function alters nucleotide ratios within both the ribo-and deoxyribo-3 6 nucleotide pools, and causes stalling of RNA polymerase, which is also known to activate 3 7 ATR. Unexpectedly, atl-1 mutants confronted with mitochondrial ETC disruption maintain normal levels 3 8 of oxygen consumption and have an increased abundance of translating ribosomes. This suggests 3 9 checkpoint signaling by ATL-1 normally dampens cytoplasmic translation. Taken together, our data 4 0 suggests a model whereby ETC insufficiency in C. elegans results in nucleotide imbalances leading to 4 1 stalling of RNA polymerase, activation of ATL-1, dampening of global translation and magnification of 4 2 ETC dysfunction. Loss of ATL-1 effectively reverses the severity of ETC disruption so that animals 4 3 become phenotypically closer to wild type.