| Literature DB >> 36266689 |
Jichen Chen1, Hong Du1, Zidong Liu1, Tangcheng Li1, Hua Du1, Wanna Wang1, Muhammad Aslam1, Weizhou Chen1, Ping Li1, Haodong Luo1, Hao Fang1, Xiaojuan Liu2.
Abstract
Tunicamycin inhibits the first step of protein N-glycosylation modification. However, the physiological, transcriptomic, and N-glycomic effects of tunicamycin on important marine diatom Phaeodactylum tricornutum are still unknown. In this study, comprehensive approaches were used to study the effects of tunicamycin stress. The results showed that cell growth and photosynthesis were significantly inhibited in P. tricornutum under the tunicamycin stress. The soluble protein content was significantly decreased, while the soluble sugar and neutral lipid were dramatically increased to orchestrate the balance of carbon and nitrogen metabolisms. The stress of 0.3 μg ml-1 tunicamycin resulted in the differential expression of ERQC and ERAD related genes. The upregulation of genes involved in ERQC pathway, the activation of anti-oxidases and the differential expression of genes related with ERAD mechanism might be important for maintaining homeostasis in cell. The identification of N-glycans, especially complex-type N-glycan structures enriched the N-glycan database of diatom P. tricornutum and provided important information for studying the function of N-glycosylation modification on proteins. As a whole, our study proposed working models of ERQC and ERAD will provide a solid foundation for further in-depth study of the related mechanism and the diatom expression system.Entities:
Keywords: ER-associated degradation; ER-quality control; N-glycan; N-glycosylation modification; Phaeodactylum tricornutum; Tunicamycin
Mesh:
Substances:
Year: 2022 PMID: 36266689 PMCID: PMC9585838 DOI: 10.1186/s12934-022-01941-y
Source DB: PubMed Journal: Microb Cell Fact ISSN: 1475-2859 Impact factor: 6.352