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Syntaxin 17, an ancient SNARE paralog, plays different and conserved roles in different organisms.
Kato, Shun; Arasaki, Kohei; Tokutomi, Natsuki; Imai, Yuzuru; Inoshita, Tsuyoshi; Hattori, Nobutaka; Sasaki, Taeko; Sato, Miyuki; Wakana, Yuichi; Inoue, Hiroki; Tagaya, Mitsuo.
Afiliación
  • Kato S; School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo 192-0392, Japan.
  • Arasaki K; School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo 192-0392, Japan.
  • Tokutomi N; School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo 192-0392, Japan.
  • Imai Y; Department of Research for Parkinson's Disease, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
  • Inoshita T; Department of Neurology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
  • Hattori N; Department of Neurodegenerative and Demented Disorders, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
  • Sasaki T; Department of Research for Parkinson's Disease, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
  • Sato M; Department of Neurology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
  • Wakana Y; Department of Neurodegenerative and Demented Disorders, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
  • Inoue H; Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan.
  • Tagaya M; Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan.
J Cell Sci ; 134(22)2021 11 15.
Article en En | MEDLINE | ID: mdl-34704591
ABSTRACT
Mammalian syntaxin 17 (Stx17) has several roles in processes other than membrane fusion, including in mitochondrial division, autophagosome formation and lipid droplet expansion. In contrast to conventional syntaxins, Stx17 has a long C-terminal hydrophobic region with a hairpin-like structure flanked by a basic amino acid-enriched C-terminal tail. Although Stx17 is one of the six ancient SNAREs and is present in diverse eukaryotic organisms, it has been lost in multiple lineages during evolution. In the present study, we compared the localization and function of fly and nematode Stx17s expressed in HeLa cells with those of human Stx17. We found that fly Stx17 predominantly localizes to the cytosol and mediates autophagy, but not mitochondrial division. Nematode Stx17, on the other hand, is predominantly present in mitochondria and facilitates mitochondrial division, but is irrelevant to autophagy. These differences are likely due to different structures in the C-terminal tail. Non-participation of fly Stx17 and nematode Stx17 in mitochondrial division and autophagy, respectively, was demonstrated in individual organisms. Our results provide an insight into the evolution of Stx17 in metazoa. This article has an associated First Person interview with the first author of the paper.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas SNARE / Fusión de Membrana Límite: Animals / Humans Idioma: En Revista: J Cell Sci Año: 2021 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas SNARE / Fusión de Membrana Límite: Animals / Humans Idioma: En Revista: J Cell Sci Año: 2021 Tipo del documento: Article País de afiliación: Japón