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Micro and macroevolution of sea anemone venom phenotype
Venom is a complex trait with substantial inter- and intraspecific variability resulting from strong selective pressures acting on the expression of many toxic proteins. However, understanding the processes underlying toxin expression dynamics that determine the venom phenotype remains unresolved. B...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842752/ https://www.ncbi.nlm.nih.gov/pubmed/36646703 http://dx.doi.org/10.1038/s41467-023-35794-9 |
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author | Smith, Edward G. Surm, Joachim M. Macrander, Jason Simhi, Adi Amir, Guy Sachkova, Maria Y. Lewandowska, Magda Reitzel, Adam M. Moran, Yehu |
author_facet | Smith, Edward G. Surm, Joachim M. Macrander, Jason Simhi, Adi Amir, Guy Sachkova, Maria Y. Lewandowska, Magda Reitzel, Adam M. Moran, Yehu |
author_sort | Smith, Edward G. |
collection | PubMed |
description | Venom is a complex trait with substantial inter- and intraspecific variability resulting from strong selective pressures acting on the expression of many toxic proteins. However, understanding the processes underlying toxin expression dynamics that determine the venom phenotype remains unresolved. By interspecific comparisons we reveal that toxin expression in sea anemones evolves rapidly and that in each species different toxin family dictates the venom phenotype by massive gene duplication events. In-depth analysis of the sea anemone, Nematostella vectensis, revealed striking variation of the dominant toxin (Nv1) diploid copy number across populations (1-24 copies) resulting from independent expansion/contraction events, which generate distinct haplotypes. Nv1 copy number correlates with expression at both the transcript and protein levels with one population having a near-complete loss of Nv1 production. Finally, we establish the dominant toxin hypothesis which incorporates observations in other venomous lineages that animals have convergently evolved a similar strategy in shaping their venom. |
format | Online Article Text |
id | pubmed-9842752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98427522023-01-18 Micro and macroevolution of sea anemone venom phenotype Smith, Edward G. Surm, Joachim M. Macrander, Jason Simhi, Adi Amir, Guy Sachkova, Maria Y. Lewandowska, Magda Reitzel, Adam M. Moran, Yehu Nat Commun Article Venom is a complex trait with substantial inter- and intraspecific variability resulting from strong selective pressures acting on the expression of many toxic proteins. However, understanding the processes underlying toxin expression dynamics that determine the venom phenotype remains unresolved. By interspecific comparisons we reveal that toxin expression in sea anemones evolves rapidly and that in each species different toxin family dictates the venom phenotype by massive gene duplication events. In-depth analysis of the sea anemone, Nematostella vectensis, revealed striking variation of the dominant toxin (Nv1) diploid copy number across populations (1-24 copies) resulting from independent expansion/contraction events, which generate distinct haplotypes. Nv1 copy number correlates with expression at both the transcript and protein levels with one population having a near-complete loss of Nv1 production. Finally, we establish the dominant toxin hypothesis which incorporates observations in other venomous lineages that animals have convergently evolved a similar strategy in shaping their venom. Nature Publishing Group UK 2023-01-16 /pmc/articles/PMC9842752/ /pubmed/36646703 http://dx.doi.org/10.1038/s41467-023-35794-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Smith, Edward G. Surm, Joachim M. Macrander, Jason Simhi, Adi Amir, Guy Sachkova, Maria Y. Lewandowska, Magda Reitzel, Adam M. Moran, Yehu Micro and macroevolution of sea anemone venom phenotype |
title | Micro and macroevolution of sea anemone venom phenotype |
title_full | Micro and macroevolution of sea anemone venom phenotype |
title_fullStr | Micro and macroevolution of sea anemone venom phenotype |
title_full_unstemmed | Micro and macroevolution of sea anemone venom phenotype |
title_short | Micro and macroevolution of sea anemone venom phenotype |
title_sort | micro and macroevolution of sea anemone venom phenotype |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842752/ https://www.ncbi.nlm.nih.gov/pubmed/36646703 http://dx.doi.org/10.1038/s41467-023-35794-9 |
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