The induction of the mitochondrial unfolded protein response (UPRmt) results in increased transcription of the gene encoding the mitochondrial chaperone HSP70. We systematically screened the C. elegans genome and identified 171 genes that, when knocked down, induce the expression of an hsp-6 HSP70 reporter and encode mitochondrial proteins. These genes represent many, but not all, mitochondrial processes (e.g., mitochondrial calcium homeostasis and mitophagy are not represented). Knockdown of these genes leads to reduced mitochondrial membrane potential and, hence, decreased protein import into mitochondria. In addition, it induces UPRmt in a manner that is dependent on ATFS-1 but that is not antagonized by the kinase GCN-2. We propose that compromised mitochondrial protein import signals the induction of UPRmt and that the mitochondrial targeting sequence of ATFS-1 functions as a sensor for this signal.
Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans/metabolism , Calcium/metabolism , Mitochondria/metabolism , Mitochondrial Proteins/metabolism , Protein Kinases/metabolism , Transcription Factors/metabolism , Unfolded Protein Response , Animals , Caenorhabditis elegans/genetics , Caenorhabditis elegans/growth & development , Caenorhabditis elegans Proteins/genetics , Membrane Potential, Mitochondrial , Mitochondria/pathology , Mitochondrial Proteins/genetics , Protein Kinases/genetics , Protein Transport , Stress, Physiological , Transcription Factors/genetics
