
ABSTRACT We describe phylogenetic and functional studies of three septins in the free-living ciliate Tetrahymena thermophila . Both deletion and overproduction of septins led to vacuolization of mitochondria, destabilization of the nuclear envelope, and increased autophagy. All three green fluorescent protein-tagged septins localized to mitochondria. Specific septins localized to the outer mitochondrial membrane, to septa formed during mitochondrial scission, or to the mitochondrion-associated endoplasmic reticulum. The only other septins known to localize to mitochondria are human ARTS and murine M-septin, both alternatively spliced forms of Sep4 (S. Larisch, Cell Cycle 3:1021-1023, 2004; S. Takahashi, R. Inatome, H. Yamamura, and S. Yanagi, Genes Cells 8:81-93, 2003). It therefore appears that septins have been recruited to mitochondrial functions independently in at least two eukaryotic lineages and in both cases are involved in apoptotic events.
Green Fluorescent Proteins, Protozoan Proteins, Apoptosis, Endoplasmic Reticulum, Mitochondria, Tetrahymena thermophila, Evolution, Molecular, Cytoskeletal Proteins, Microscopy, Electron, Transmission, Mitochondrial Membranes, Animals
Green Fluorescent Proteins, Protozoan Proteins, Apoptosis, Endoplasmic Reticulum, Mitochondria, Tetrahymena thermophila, Evolution, Molecular, Cytoskeletal Proteins, Microscopy, Electron, Transmission, Mitochondrial Membranes, Animals
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