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Drosophila CTP synthase can form distinct substrate- and product-bound filaments.
Zhou, Xian; Guo, Chen-Jun; Hu, Huan-Huan; Zhong, Jiale; Sun, Qianqian; Liu, Dandan; Zhou, Shuang; Chang, Chia Chun; Liu, Ji-Long.
Afiliación
  • Zhou X; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
  • Guo CJ; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
  • Hu HH; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China; Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, 200031, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Zhong J; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China; Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, 200031, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Sun Q; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China; iHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
  • Liu D; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China; iHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
  • Zhou S; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China; Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, 200031, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Chang CC; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
  • Liu JL; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China. Electronic address: liujl3@shanghaitech.edu.cn.
J Genet Genomics ; 46(11): 537-545, 2019 11 20.
Article en En | MEDLINE | ID: mdl-31902586
ABSTRACT
Intracellular compartmentation is a key strategy for the functioning of a cell. In 2010, several studies revealed that the metabolic enzyme CTP synthase (CTPS) can form filamentous structures termed cytoophidia in prokaryotic and eukaryotic cells. However, recent structural studies showed that CTPS only forms inactive product-bound filaments in bacteria while forming active substrate-bound filaments in eukaryotic cells. In this study, using negative staining and cryo-electron microscopy, we demonstrate that Drosophila CTPS, whether in substrate-bound or product-bound form, can form filaments. Our results challenge the previous model and indicate that substrate-bound and product-bound filaments can coexist in the same species. We speculate that the ability to switch between active and inactive cytoophidia in the same cells provides an additional layer of metabolic regulation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ligasas de Carbono-Nitrógeno / Proteínas de Drosophila Límite: Animals Idioma: En Revista: J Genet Genomics Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ligasas de Carbono-Nitrógeno / Proteínas de Drosophila Límite: Animals Idioma: En Revista: J Genet Genomics Año: 2019 Tipo del documento: Article País de afiliación: China
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