Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway

Interleukin-1 receptor-associated kinases (IRAKs) play important roles in MyD88-dependent TLR signaling, the crucial innate immune pathway in molluscs. In this study, we examined the full-length IRAK4 genetic sequence in the Pacific oyster (Crassostrea gigas) by molecular cloning. Phylogenetic analy...

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Published in:Developmental & Comparative Immunology
Main Authors: Tang, Xueying, Huang, Baoyu, Zhang, Linlin, Li, Li, Zhang, Guofan
Format: Article in Journal/Newspaper
Language:English
Published: 2017
Subjects:
Tlr
Online Access:http://ir.qdio.ac.cn/handle/337002/137057
https://doi.org/10.1016/j.dci.2017.02.004
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spelling ftchinacasciocas:oai:ir.qdio.ac.cn:337002/137057 2023-05-15T15:57:35+02:00 Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway Tang, Xueying Huang, Baoyu Zhang, Linlin Li, Li Zhang, Guofan 2017-07-01 http://ir.qdio.ac.cn/handle/337002/137057 https://doi.org/10.1016/j.dci.2017.02.004 英语 eng DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY Tang, Xueying,Huang, Baoyu,Zhang, Linlin,et al. Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway[J]. DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY,2017,72:21-29. http://ir.qdio.ac.cn/handle/337002/137057 doi:10.1016/j.dci.2017.02.004 Crassostrea Gigas Irak4 Myd88 Tlr Nf-kappa b Article 期刊论文 2017 ftchinacasciocas https://doi.org/10.1016/j.dci.2017.02.004 2022-06-27T05:38:04Z Interleukin-1 receptor-associated kinases (IRAKs) play important roles in MyD88-dependent TLR signaling, the crucial innate immune pathway in molluscs. In this study, we examined the full-length IRAK4 genetic sequence in the Pacific oyster (Crassostrea gigas) by molecular cloning. Phylogenetic analysis revealed that CgIRAK4 is most closely related to Mytilus edulis, and forms a Glade with other molluscs. CgIRAK4 transcripts are widely expressed in all tissues, with the highest expression observed in the hemocytes and gill. Moreover, CgIRAK4 is significantly upregulated after Oyster herpesvirus-1 microvariant (0sHV-1 mu var), Vibrio alginolyticus, and poly I:C challenge. Yeast two-hybrid and co-immunoprecipitation assays reveal that the CgIRAK4 death domain is necessary to mediate interaction between CgIRAK4 and two CgMyD88 isoforms. In addition, CgIRAK4 overexpression cannot induce NF-kappa B transcriptional activity, but blocks that induced by CgMyD88 in HEK293T cells. These findings elucidate the mechanisms of MyD88-dependent TLR signaling in molluscs, and the differences in IRAK-mediated pathway activation between invertebrates and vertebrates. (C) 2017 Elsevier Ltd. All rights reserved. Article in Journal/Newspaper Crassostrea gigas Pacific oyster Institute of Oceanology, Chinese Academy of Sciences: IOCAS-IR Pacific Developmental & Comparative Immunology 72 21 29
institution Open Polar
collection Institute of Oceanology, Chinese Academy of Sciences: IOCAS-IR
op_collection_id ftchinacasciocas
language English
topic Crassostrea Gigas
Irak4
Myd88
Tlr
Nf-kappa b
spellingShingle Crassostrea Gigas
Irak4
Myd88
Tlr
Nf-kappa b
Tang, Xueying
Huang, Baoyu
Zhang, Linlin
Li, Li
Zhang, Guofan
Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway
topic_facet Crassostrea Gigas
Irak4
Myd88
Tlr
Nf-kappa b
description Interleukin-1 receptor-associated kinases (IRAKs) play important roles in MyD88-dependent TLR signaling, the crucial innate immune pathway in molluscs. In this study, we examined the full-length IRAK4 genetic sequence in the Pacific oyster (Crassostrea gigas) by molecular cloning. Phylogenetic analysis revealed that CgIRAK4 is most closely related to Mytilus edulis, and forms a Glade with other molluscs. CgIRAK4 transcripts are widely expressed in all tissues, with the highest expression observed in the hemocytes and gill. Moreover, CgIRAK4 is significantly upregulated after Oyster herpesvirus-1 microvariant (0sHV-1 mu var), Vibrio alginolyticus, and poly I:C challenge. Yeast two-hybrid and co-immunoprecipitation assays reveal that the CgIRAK4 death domain is necessary to mediate interaction between CgIRAK4 and two CgMyD88 isoforms. In addition, CgIRAK4 overexpression cannot induce NF-kappa B transcriptional activity, but blocks that induced by CgMyD88 in HEK293T cells. These findings elucidate the mechanisms of MyD88-dependent TLR signaling in molluscs, and the differences in IRAK-mediated pathway activation between invertebrates and vertebrates. (C) 2017 Elsevier Ltd. All rights reserved.
format Article in Journal/Newspaper
author Tang, Xueying
Huang, Baoyu
Zhang, Linlin
Li, Li
Zhang, Guofan
author_facet Tang, Xueying
Huang, Baoyu
Zhang, Linlin
Li, Li
Zhang, Guofan
author_sort Tang, Xueying
title Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway
title_short Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway
title_full Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway
title_fullStr Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway
title_full_unstemmed Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway
title_sort molecular characterization of pacific oyster (crassostrea gigas) irak4 gene and its role in myd88-dependent pathway
publishDate 2017
url http://ir.qdio.ac.cn/handle/337002/137057
https://doi.org/10.1016/j.dci.2017.02.004
geographic Pacific
geographic_facet Pacific
genre Crassostrea gigas
Pacific oyster
genre_facet Crassostrea gigas
Pacific oyster
op_relation DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
Tang, Xueying,Huang, Baoyu,Zhang, Linlin,et al. Molecular characterization of Pacific oyster (Crassostrea gigas) IRAK4 gene and its role in MyD88-dependent pathway[J]. DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY,2017,72:21-29.
http://ir.qdio.ac.cn/handle/337002/137057
doi:10.1016/j.dci.2017.02.004
op_doi https://doi.org/10.1016/j.dci.2017.02.004
container_title Developmental & Comparative Immunology
container_volume 72
container_start_page 21
op_container_end_page 29
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