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Functions and substrates of NEDDylation during cell cycle in the silkworm, Bombyx mori.
Li, Zhiqing; Cui, Qixin; Wang, Xiaoyan; Li, Bingqian; Zhao, Dongchao; Xia, Qingyou; Zhao, Ping.
Affiliation
  • Li Z; State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China; Chongqing Engineering and Technology Research Center for Novel Silk Materials, Chongqing, China.
  • Cui Q; State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
  • Wang X; State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
  • Li B; State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
  • Zhao D; State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
  • Xia Q; State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China; Chongqing Engineering and Technology Research Center for Novel Silk Materials, Chongqing, China.
  • Zhao P; State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China; Chongqing Engineering and Technology Research Center for Novel Silk Materials, Chongqing, China. Electronic address: zhaop@swu.edu.cn.
Insect Biochem Mol Biol ; 90: 101-112, 2017 11.
Article in En | MEDLINE | ID: mdl-28964913
ABSTRACT
NEDDylation, a post-translational modification mediated by the conjugation of the ubiquitin-like protein Nedd8 to specific substrates, is an essential biological process that regulates cell cycle progression in eukaryotes. Here, we report the conservation of NEDDylation machinery and NEDDylated proteins in the silkworm, Bombyx mori. We have identified all the components necessary for reversible NEDDylation in the silkworm including Nedd8, E1, E2, E3, and deNEDDylation enzymes. By the approach of RNAi-mediated gene silencing, it was shown that knockdown of BmNedd8 and the conjugating enzymes decreased the global level of NEDDylation, while knockdown of deNEDDylation enzymes increased the prevalence of this modification in cultured silkworm cells. Moreover, the lack of the NEDDylation system caused cell cycle arrest at the G2/M phase and resulted in defects in chromosome congression and segregation. Using the wild-type and mutants of BmNedd8, we identified the specific substrates of BmNedd8, which are involved in the regulation for many cellular processes, including ribosome biogenesis, spliceosome structure, spindle formation, metabolism, and RNA biogenesis. This clearly demonstrates that the NEDDylation system is able to control multiple pathways in the silkworm. Altogether, the information on the functions and substrates of the NEDDylation system presented here could provide a basis for future investigations of protein NEDDylation and its regulatory mechanism on cell cycle progression in the silkworm.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bombyx / Cell Cycle / Insect Proteins / NEDD8 Protein Type of study: Risk_factors_studies Limits: Animals Language: En Journal: Insect Biochem Mol Biol Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA Year: 2017 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bombyx / Cell Cycle / Insect Proteins / NEDD8 Protein Type of study: Risk_factors_studies Limits: Animals Language: En Journal: Insect Biochem Mol Biol Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA Year: 2017 Document type: Article Affiliation country: China