Functional relationship between CgMyD88-1 and CgMyD88-2 in the Pacific oyster

MyD88 is a universal adapter protein for the Toll-like receptor/interleukin-1 receptor (TLR/IL-1R) signaling pathway. Since invertebrates are believed to lack MyD88-independent pathways, MyD88 appears more critical in oyster TLR signaling pathway. In the Pacific oyster (Crassostrea gigas), two compl...

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Published in:Fish & Shellfish Immunology
Main Authors: Tang, Xueying, Huang, Baoyu, Lin, Siheng, Wang, Wei, Zhang, Guofan, Li, Li
Format: Report
Language:English
Published: ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD 2020
Subjects:
Online Access:http://ir.qdio.ac.cn/handle/337002/164483
https://doi.org/10.1016/j.fsi.2019.10.060
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spelling ftchinacasciocas:oai:ir.qdio.ac.cn:337002/164483 2023-05-15T15:57:48+02:00 Functional relationship between CgMyD88-1 and CgMyD88-2 in the Pacific oyster Tang, Xueying Huang, Baoyu Lin, Siheng Wang, Wei Zhang, Guofan Li, Li 2020 http://ir.qdio.ac.cn/handle/337002/164483 https://doi.org/10.1016/j.fsi.2019.10.060 英语 eng ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD FISH & SHELLFISH IMMUNOLOGY http://ir.qdio.ac.cn/handle/337002/164483 doi:10.1016/j.fsi.2019.10.060 Crassostrea gigas Innate immunity MyD88 Functional diversity Fisheries Immunology Marine & Freshwater Biology Veterinary Sciences FACTOR 88 MYD88 IDENTIFICATION GENOME 期刊论文 2020 ftchinacasciocas https://doi.org/10.1016/j.fsi.2019.10.060 2022-06-27T05:41:43Z MyD88 is a universal adapter protein for the Toll-like receptor/interleukin-1 receptor (TLR/IL-1R) signaling pathway. Since invertebrates are believed to lack MyD88-independent pathways, MyD88 appears more critical in oyster TLR signaling pathway. In the Pacific oyster (Crassostrea gigas), two complete paralogues, named as CgMyD88-1 and CgMyD88-2, have been identified. In the current study, we indicated that CgMyD88-1 and CgMyD88-2 might act synergistically to increase the efficiency of immune signaling by activating NF-kappa B transcription factor. However, we found that upon stimulation with lipopolysaccharide (LPS) or polyinosinic:polycytidylic acid [poly (I:C)], CgMyD88-1 and CgMyD88-2 show differences in their response: CgMyD88-1 accumulated as large spots in the cytoplasm, while CgMyD88-2 assembled in the cytoplasm and in the membrane. Our results support the theory that expansion of these immune genes is associated with functional diversity. Report Crassostrea gigas Pacific oyster Institute of Oceanology, Chinese Academy of Sciences: IOCAS-IR Pacific Fish & Shellfish Immunology 96 138 140
institution Open Polar
collection Institute of Oceanology, Chinese Academy of Sciences: IOCAS-IR
op_collection_id ftchinacasciocas
language English
topic Crassostrea gigas
Innate immunity
MyD88
Functional diversity
Fisheries
Immunology
Marine & Freshwater Biology
Veterinary Sciences
FACTOR 88 MYD88
IDENTIFICATION
GENOME
spellingShingle Crassostrea gigas
Innate immunity
MyD88
Functional diversity
Fisheries
Immunology
Marine & Freshwater Biology
Veterinary Sciences
FACTOR 88 MYD88
IDENTIFICATION
GENOME
Tang, Xueying
Huang, Baoyu
Lin, Siheng
Wang, Wei
Zhang, Guofan
Li, Li
Functional relationship between CgMyD88-1 and CgMyD88-2 in the Pacific oyster
topic_facet Crassostrea gigas
Innate immunity
MyD88
Functional diversity
Fisheries
Immunology
Marine & Freshwater Biology
Veterinary Sciences
FACTOR 88 MYD88
IDENTIFICATION
GENOME
description MyD88 is a universal adapter protein for the Toll-like receptor/interleukin-1 receptor (TLR/IL-1R) signaling pathway. Since invertebrates are believed to lack MyD88-independent pathways, MyD88 appears more critical in oyster TLR signaling pathway. In the Pacific oyster (Crassostrea gigas), two complete paralogues, named as CgMyD88-1 and CgMyD88-2, have been identified. In the current study, we indicated that CgMyD88-1 and CgMyD88-2 might act synergistically to increase the efficiency of immune signaling by activating NF-kappa B transcription factor. However, we found that upon stimulation with lipopolysaccharide (LPS) or polyinosinic:polycytidylic acid [poly (I:C)], CgMyD88-1 and CgMyD88-2 show differences in their response: CgMyD88-1 accumulated as large spots in the cytoplasm, while CgMyD88-2 assembled in the cytoplasm and in the membrane. Our results support the theory that expansion of these immune genes is associated with functional diversity.
format Report
author Tang, Xueying
Huang, Baoyu
Lin, Siheng
Wang, Wei
Zhang, Guofan
Li, Li
author_facet Tang, Xueying
Huang, Baoyu
Lin, Siheng
Wang, Wei
Zhang, Guofan
Li, Li
author_sort Tang, Xueying
title Functional relationship between CgMyD88-1 and CgMyD88-2 in the Pacific oyster
title_short Functional relationship between CgMyD88-1 and CgMyD88-2 in the Pacific oyster
title_full Functional relationship between CgMyD88-1 and CgMyD88-2 in the Pacific oyster
title_fullStr Functional relationship between CgMyD88-1 and CgMyD88-2 in the Pacific oyster
title_full_unstemmed Functional relationship between CgMyD88-1 and CgMyD88-2 in the Pacific oyster
title_sort functional relationship between cgmyd88-1 and cgmyd88-2 in the pacific oyster
publisher ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
publishDate 2020
url http://ir.qdio.ac.cn/handle/337002/164483
https://doi.org/10.1016/j.fsi.2019.10.060
geographic Pacific
geographic_facet Pacific
genre Crassostrea gigas
Pacific oyster
genre_facet Crassostrea gigas
Pacific oyster
op_relation FISH & SHELLFISH IMMUNOLOGY
http://ir.qdio.ac.cn/handle/337002/164483
doi:10.1016/j.fsi.2019.10.060
op_doi https://doi.org/10.1016/j.fsi.2019.10.060
container_title Fish & Shellfish Immunology
container_volume 96
container_start_page 138
op_container_end_page 140
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