| Literature DB >> 31412237 |
Stéphane G Rolland1, Sandra Schneid2, Melanie Schwarz2, Elisabeth Rackles2, Christian Fischer3, Simon Haeussler2, Saroj G Regmi2, Assa Yeroslaviz4, Bianca Habermann4, Dejana Mokranjac5, Eric Lambie2, Barbara Conradt6.
Abstract
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.Entities:
Keywords: ATFS-1; C. elegans; GCN-2; UPR(mt); hsp-6; hsp-60; mitochondria
Mesh:
Substances:
Year: 2019 PMID: 31412237 DOI: 10.1016/j.celrep.2019.07.049
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423