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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4346834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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