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Massive expansion and functional divergence of innate immune genes in a protostome

The molecules that mediate innate immunity are encoded by relatively few genes and exhibit broad specificity. Detailed annotation of the Pacific oyster (Crassostrea gigas) genome, a protostome invertebrate, reveals large-scale duplication and divergence of multigene families encoding molecules that...

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Autores principales: Zhang, Linlin, Li, Li, Guo, Ximing, Litman, Gary W., Dishaw, Larry J., Zhang, Guofan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346834/
https://www.ncbi.nlm.nih.gov/pubmed/25732911
http://dx.doi.org/10.1038/srep08693
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author Zhang, Linlin
Li, Li
Guo, Ximing
Litman, Gary W.
Dishaw, Larry J.
Zhang, Guofan
author_facet Zhang, Linlin
Li, Li
Guo, Ximing
Litman, Gary W.
Dishaw, Larry J.
Zhang, Guofan
author_sort Zhang, Linlin
collection PubMed
description The molecules that mediate innate immunity are encoded by relatively few genes and exhibit broad specificity. Detailed annotation of the Pacific oyster (Crassostrea gigas) genome, a protostome invertebrate, reveals large-scale duplication and divergence of multigene families encoding molecules that effect innate immunity. Transcriptome analyses indicate dynamic and orchestrated specific expression of numerous innate immune genes in response to experimental challenge with pathogens, including bacteria, and a pathogenic virus. Variable expression of individual members of the multigene families encoding these genes also occurs during different types of abiotic stress (environmentally-equivalent conditions of temperature, salinity and desiccation). Multiple families of immune genes are responsive in concert to certain biotic and abiotic challenges. Individual members of expanded families of immune genes are differentially expressed under both biotic challenge and abiotic stress conditions. Members of the same families of innate immune molecules also are transcribed in developmental stage- and tissue-specific manners. An integrated, highly complex innate immune system that exhibits remarkable discriminatory properties and responses to different pathogens as well as environmental stress has arisen through the adaptive recruitment of tandem duplicated genes. The co-adaptive evolution of stress and innate immune responses appears to have an ancient origin in phylogeny.
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spelling pubmed-43468342015-03-10 Massive expansion and functional divergence of innate immune genes in a protostome Zhang, Linlin Li, Li Guo, Ximing Litman, Gary W. Dishaw, Larry J. Zhang, Guofan Sci Rep Article The molecules that mediate innate immunity are encoded by relatively few genes and exhibit broad specificity. Detailed annotation of the Pacific oyster (Crassostrea gigas) genome, a protostome invertebrate, reveals large-scale duplication and divergence of multigene families encoding molecules that effect innate immunity. Transcriptome analyses indicate dynamic and orchestrated specific expression of numerous innate immune genes in response to experimental challenge with pathogens, including bacteria, and a pathogenic virus. Variable expression of individual members of the multigene families encoding these genes also occurs during different types of abiotic stress (environmentally-equivalent conditions of temperature, salinity and desiccation). Multiple families of immune genes are responsive in concert to certain biotic and abiotic challenges. Individual members of expanded families of immune genes are differentially expressed under both biotic challenge and abiotic stress conditions. Members of the same families of innate immune molecules also are transcribed in developmental stage- and tissue-specific manners. An integrated, highly complex innate immune system that exhibits remarkable discriminatory properties and responses to different pathogens as well as environmental stress has arisen through the adaptive recruitment of tandem duplicated genes. The co-adaptive evolution of stress and innate immune responses appears to have an ancient origin in phylogeny. Nature Publishing Group 2015-03-03 /pmc/articles/PMC4346834/ /pubmed/25732911 http://dx.doi.org/10.1038/srep08693 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhang, Linlin
Li, Li
Guo, Ximing
Litman, Gary W.
Dishaw, Larry J.
Zhang, Guofan
Massive expansion and functional divergence of innate immune genes in a protostome
title Massive expansion and functional divergence of innate immune genes in a protostome
title_full Massive expansion and functional divergence of innate immune genes in a protostome
title_fullStr Massive expansion and functional divergence of innate immune genes in a protostome
title_full_unstemmed Massive expansion and functional divergence of innate immune genes in a protostome
title_short Massive expansion and functional divergence of innate immune genes in a protostome
title_sort massive expansion and functional divergence of innate immune genes in a protostome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346834/
https://www.ncbi.nlm.nih.gov/pubmed/25732911
http://dx.doi.org/10.1038/srep08693
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