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Molecular Bases of Disease
2 Results
- Molecular Bases of DiseaseOpen Access
Mitochondrial calcium uniporter in Drosophila transfers calcium between the endoplasmic reticulum and mitochondria in oxidative stress-induced cell death
Journal of Biological ChemistryVol. 292Issue 35p14473–14485Published online: July 18, 2017- Sekyu Choi
- Xianglan Quan
- Sunhoe Bang
- Heesuk Yoo
- Jiyoung Kim
- Jiwon Park
- and others
Cited in Scopus: 29Mitochondrial calcium plays critical roles in diverse cellular processes ranging from energy metabolism to cell death. Previous studies have demonstrated that mitochondrial calcium uptake is mainly mediated by the mitochondrial calcium uniporter (MCU) complex. However, the roles of the MCU complex in calcium transport, signaling, and dysregulation by oxidative stress still remain unclear. Here, we confirmed that Drosophila MCU contains evolutionarily conserved structures and requires essential MCU regulator (EMRE) for its calcium channel activities. - Molecular Bases of DiseaseOpen Access
Tumor Necrosis Factor Receptor-associated Protein 1 (TRAP1) Mutation and TRAP1 Inhibitor Gamitrinib-triphenylphosphonium (G-TPP) Induce a Forkhead Box O (FOXO)-dependent Cell Protective Signal from Mitochondria
Journal of Biological ChemistryVol. 291Issue 4p1841–1853Published online: December 2, 2015- Hyunjin Kim
- Jinsung Yang
- Min Ju Kim
- Sekyu Choi
- Ju-Ryung Chung
- Jong-Min Kim
- and others
Cited in Scopus: 32TRAP1 (tumor necrosis factor receptor-associated protein 1), a mitochondrial Hsp90 family chaperone, has been identified as a critical regulator of cell survival and bioenergetics in tumor cells. To discover novel signaling networks regulated by TRAP1, we generated Drosophila TRAP1 mutants. The mutants successfully developed into adults and produced fertile progeny, showing that TRAP1 is dispensable in development and reproduction. Surprisingly, mutation or knockdown of TRAP1 markedly enhanced Drosophila survival under oxidative stress.