Literature DB >> 33519851

Endoplasmic Reticulum-Mediated Protein Quality Control and Endoplasmic Reticulum-Associated Degradation Pathway Explain the Reduction of N-glycoprotein Level Under the Lead Stress.

Hong Du1,2, Canqi Zheng1,2, Muhmmad Aslam1,2,3, Xihui Xie1,2, Wanna Wang1,2, Yingquan Yang1,2, Xiaojuan Liu1,2.   

Abstract

Different anthropogenic activities result in the continuous increase of metal lead (Pb) in the environment and adversely affect living organisms. Therefore, it is important to investigate the tolerance mechanism in a model organism. Chlamydomonas reinhardtii is an important green eukaryotic model microalga for studying different kinds of biological questions. In this study, the responses of C. reinhardtii were revealed via a comprehensive approach, including physiological, genomic, transcriptomic, glycomic, and bioinformatic techniques. Physiological results showed that the growth rate and soluble protein content were significantly reduced under the high lead stress. Also, the results obtained from the genomic and transcriptomic analyses presented that the endoplasmic reticulum-mediated protein quality control (ERQC) system and endoplasmic reticulum-associated degradation (ERAD) pathway were activated under the third day of high lead stress. The unique upregulated protein disulfide isomerase genes on the ERQC system were proposed to be important for the protein level and protein quality control. The accumulation of specific N-glycans indicated that specific N-glycosylation of proteins might alter the biological functions of proteins to alleviate the Pb stress in alga and/or lead to the degradation of incomplete/misfolded proteins. At the same time, it was observed that genes involved in each process of ERAD were upregulated, suggesting that the ERAD pathway was activated to assist the degradation of incomplete/misfolded proteins. Therefore, it is reasonable to speculate that the reduction of protein level under the high lead stress was related to the activated ERQC system and QRAD pathway. Our findings will provide a solid and reliable foundation and a proposed ERAD working model for further in-depth study of the ERQC system and ERAD pathway under the Pb stress and even other biotic and abiotic stresses.
Copyright © 2021 Du, Zheng, Aslam, Xie, Wang, Yang and Liu.

Entities:  

Keywords:  ER-associated degradation pathway; ER-mediated protein quality control; N-glycan; lead; protein level

Year:  2021        PMID: 33519851      PMCID: PMC7838096          DOI: 10.3389/fpls.2020.598552

Source DB:  PubMed          Journal:  Front Plant Sci        ISSN: 1664-462X            Impact factor:   5.753


  3 in total

1.  Endoplasmic reticulum-quality control pathway and endoplasmic reticulum-associated degradation mechanism regulate the N-glycoproteins and N-glycan structures in the diatom Phaeodactylum tricornutum.

Authors:  Jichen Chen; Hong Du; Zidong Liu; Tangcheng Li; Hua Du; Wanna Wang; Muhammad Aslam; Weizhou Chen; Ping Li; Haodong Luo; Hao Fang; Xiaojuan Liu
Journal:  Microb Cell Fact       Date:  2022-10-20       Impact factor: 6.352

2.  Global Profiling of N-Glycoproteins and N-Glycans in the Diatom Phaeodactylum tricornutum.

Authors:  Xihui Xie; Hong Du; Jichen Chen; Muhammad Aslam; Wanna Wang; Weizhou Chen; Ping Li; Hua Du; Xiaojuan Liu
Journal:  Front Plant Sci       Date:  2021-12-03       Impact factor: 5.753

3.  Role and mechanism of chaperones calreticulin and ERP57 in restoring trafficking to mutant HERG‑A561V protein.

Authors:  Yujia Wu; Xiaoyan Huang; Zequn Zheng; Xi Yang; Yanna Ba; Jiangfang Lian
Journal:  Int J Mol Med       Date:  2021-07-02       Impact factor: 4.101

  3 in total

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