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Identification, Characterization, and Function Analysis of the Cactus Gene from Litopenaeus vannamei

The nuclear factor-kappa B (NF-κB) pathways play important roles in innate immune responses. IκB is the main cytoplasmic inhibitor of NF-κB. In this study, we identified the LvCactus gene from Litopenaeus vannamei, which is the first cloned IκB homologue in subphylum Crustacea. LvCactus contains six...

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Autores principales: Li, Chaozheng, Chen, Yi-Xiao, Zhang, Shuang, Lü, Ling, Chen, Yi-Hong, Chai, Jiaoting, Weng, Shaoping, Chen, Yong-Gui, He, Jianguo, Xu, Xiaopeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504109/
https://www.ncbi.nlm.nih.gov/pubmed/23185415
http://dx.doi.org/10.1371/journal.pone.0049711
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author Li, Chaozheng
Chen, Yi-Xiao
Zhang, Shuang
Lü, Ling
Chen, Yi-Hong
Chai, Jiaoting
Weng, Shaoping
Chen, Yong-Gui
He, Jianguo
Xu, Xiaopeng
author_facet Li, Chaozheng
Chen, Yi-Xiao
Zhang, Shuang
Lü, Ling
Chen, Yi-Hong
Chai, Jiaoting
Weng, Shaoping
Chen, Yong-Gui
He, Jianguo
Xu, Xiaopeng
author_sort Li, Chaozheng
collection PubMed
description The nuclear factor-kappa B (NF-κB) pathways play important roles in innate immune responses. IκB is the main cytoplasmic inhibitor of NF-κB. In this study, we identified the LvCactus gene from Litopenaeus vannamei, which is the first cloned IκB homologue in subphylum Crustacea. LvCactus contains six predicted ankyrin repeats, which show similarities to those of Cactus proteins from insects. LvCactus localizes in cytoplasm and interacts with LvDorsal, an L. vannamei homologue to Drosophila melanogaster Dorsal belonging to class II NF-κB family, to prevent its nuclear translocation. Contrary to that of LvDorsal, over-expression of LvCactus down-regulates the activities of shrimp antimicrobial peptides promoters, suggesting LvCactus is an inhibitor of LvDorsal. The promoter of LvCactus was predicted to contain five putative NF-κB binding motifs, among which four were proved to be bound by LvDorsal by chromatin immunoprecipitation assays. Dual-luciferase reporter assays also showed that transcription of LvCactus was promoted by LvDorsal but inhibited by LvCactus itself, indicating a feedback regulatory pathway between LvCactus and LvDorsal. Expression of LvCactus was up-regulated after Lipopolysaccharides, poly (I:C), Vibrio parahaemolyticus, and Staphylococcus aureus injections, suggesting an activation response of LvCactus to bacterial and immune stimulant challenges. Differently, the LvCactus expression levels obviously decreased during white spot syndrome virus (WSSV) infection, indicating the feedback regulatory pathway of LvCactus/LvDorsal could be modified by WSSV.
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spelling pubmed-35041092012-11-26 Identification, Characterization, and Function Analysis of the Cactus Gene from Litopenaeus vannamei Li, Chaozheng Chen, Yi-Xiao Zhang, Shuang Lü, Ling Chen, Yi-Hong Chai, Jiaoting Weng, Shaoping Chen, Yong-Gui He, Jianguo Xu, Xiaopeng PLoS One Research Article The nuclear factor-kappa B (NF-κB) pathways play important roles in innate immune responses. IκB is the main cytoplasmic inhibitor of NF-κB. In this study, we identified the LvCactus gene from Litopenaeus vannamei, which is the first cloned IκB homologue in subphylum Crustacea. LvCactus contains six predicted ankyrin repeats, which show similarities to those of Cactus proteins from insects. LvCactus localizes in cytoplasm and interacts with LvDorsal, an L. vannamei homologue to Drosophila melanogaster Dorsal belonging to class II NF-κB family, to prevent its nuclear translocation. Contrary to that of LvDorsal, over-expression of LvCactus down-regulates the activities of shrimp antimicrobial peptides promoters, suggesting LvCactus is an inhibitor of LvDorsal. The promoter of LvCactus was predicted to contain five putative NF-κB binding motifs, among which four were proved to be bound by LvDorsal by chromatin immunoprecipitation assays. Dual-luciferase reporter assays also showed that transcription of LvCactus was promoted by LvDorsal but inhibited by LvCactus itself, indicating a feedback regulatory pathway between LvCactus and LvDorsal. Expression of LvCactus was up-regulated after Lipopolysaccharides, poly (I:C), Vibrio parahaemolyticus, and Staphylococcus aureus injections, suggesting an activation response of LvCactus to bacterial and immune stimulant challenges. Differently, the LvCactus expression levels obviously decreased during white spot syndrome virus (WSSV) infection, indicating the feedback regulatory pathway of LvCactus/LvDorsal could be modified by WSSV. Public Library of Science 2012-11-21 /pmc/articles/PMC3504109/ /pubmed/23185415 http://dx.doi.org/10.1371/journal.pone.0049711 Text en © 2012 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Li, Chaozheng
Chen, Yi-Xiao
Zhang, Shuang
Lü, Ling
Chen, Yi-Hong
Chai, Jiaoting
Weng, Shaoping
Chen, Yong-Gui
He, Jianguo
Xu, Xiaopeng
Identification, Characterization, and Function Analysis of the Cactus Gene from Litopenaeus vannamei
title Identification, Characterization, and Function Analysis of the Cactus Gene from Litopenaeus vannamei
title_full Identification, Characterization, and Function Analysis of the Cactus Gene from Litopenaeus vannamei
title_fullStr Identification, Characterization, and Function Analysis of the Cactus Gene from Litopenaeus vannamei
title_full_unstemmed Identification, Characterization, and Function Analysis of the Cactus Gene from Litopenaeus vannamei
title_short Identification, Characterization, and Function Analysis of the Cactus Gene from Litopenaeus vannamei
title_sort identification, characterization, and function analysis of the cactus gene from litopenaeus vannamei
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504109/
https://www.ncbi.nlm.nih.gov/pubmed/23185415
http://dx.doi.org/10.1371/journal.pone.0049711
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