Literature DB >> 22554476

Identification and characterization of Inositol-requiring enzyme-1 and X-box binding protein 1, two proteins involved in the unfolded protein response of Litopenaeus vannamei.

Yi-Hong Chen1, Li Zhao, Li-Ran Pang, Xiao-Yun Li, Shao-Ping Weng, Jian-Guo He.   

Abstract

The inositol-requiring enzyme-1 (IRE1)-X-box binding protein 1 (IRE1-XBP1) pathway is the key branch of the unfolded protein response (UPR). To investigate the role of the IRE1-XBP1 pathway in reducing environmental stress and increasing anti-viral immunity in Litopenaeus vannamei, homologues of IRE1 (designated as LvIRE1) and XBP1 (designated as LvXBP1) were identified and characterized. The full-length cDNA of LvIRE1 is 4908bp long, with an open reading frame (ORF) that encodies a putative 1174 amino acid protein. The full-length cDNA of LvXBP1 is 1746bp long. It contains two ORFs that encode putative 278 amino acid and 157 amino acid proteins, respectively. LvXBP1 mRNA has the predicted IRE1 splicing motifs CNG'CNGN located within the loop regions of two short hairpins. Sequencing of the splicing fragment induced by endoplasmic reticulum (ER)-stress showed a 3bp or 4bp frame shift from the predicted sites. The spliced form LvXBP1 (LvXBP1s) contained an ORF encodes a putative 463 amino acid protein. The reporter gene assays indicated that LvXBP1s activates the promoter of L. vannamei immunoglobulin heavy chain binding protein (LvBip), an important UPR effector. RT-PCR showed that LvXBP1 was spliced during the experiments. For heat shock treatment, the total LvXBP1 expression was increased and peaked at about 36h, whereas the percentages of the two isoforms were relatively stable. For the WSSV challenge, LvXBP1 was upregulated during the experiment and the percentage of the spliced form continuously declined after 18h of infection. Knock-down of LvXBP1 by RNA interference resulted in a lower cumulative mortality of L. vannamei under WSSV infection. Furthermore, the expression profiles of LvIRE1 and LvXBP1 in the gills, hemocytes, intestines, and hepatopancreas of the WSSV-challenged shrimp were detected using real-time RT-PCR. Taken together, these results confirm that the IRE1-XBP1 pathway is important for L. vannamei environmental stress resistance, suggest that L. vannamei IRE1-XBP1 may activated by WSSV and be annexed to serve the virus. Crown
Copyright © 2012. Published by Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22554476     DOI: 10.1016/j.dci.2012.04.005

Source DB:  PubMed          Journal:  Dev Comp Immunol        ISSN: 0145-305X            Impact factor:   3.636


  4 in total

1.  A Glutathione Peroxidase Gene from Litopenaeus vannamei Is Involved in Oxidative Stress Responses and Pathogen Infection Resistance.

Authors:  Jinquan Fan; Binbin Li; Qianming Hong; Zeyu Yan; Xinjun Yang; Kecheng Lu; Guoliang Chen; Lei Wang; Yihong Chen
Journal:  Int J Mol Sci       Date:  2022-01-05       Impact factor: 5.923

2.  Activating transcription factor 4 and X box binding protein 1 of Litopenaeus vannamei transcriptional regulated white spot syndrome virus genes Wsv023 and Wsv083.

Authors:  Xiao-Yun Li; Li-Ran Pang; Yong-Gui Chen; Shao-Ping Weng; Hai-Tao Yue; Ze-Zhi Zhang; Yi-Hong Chen; Jian-Guo He
Journal:  PLoS One       Date:  2013-04-24       Impact factor: 3.240

Review 3.  Molecular Mechanisms of White Spot Syndrome Virus Infection and Perspectives on Treatments.

Authors:  Bas Verbruggen; Lisa K Bickley; Ronny van Aerle; Kelly S Bateman; Grant D Stentiford; Eduarda M Santos; Charles R Tyler
Journal:  Viruses       Date:  2016-01-18       Impact factor: 5.048

4.  Investigating the physiological responses of Pacific white shrimp Litopenaeus vannamei to acute cold-stress.

Authors:  Zhenlu Wang; Yuexin Qu; Xiaolei Zhuo; Junyi Li; Jixing Zou; Lanfen Fan
Journal:  PeerJ       Date:  2019-07-24       Impact factor: 2.984

  4 in total

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