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Do novel genes drive morphological novelty? An investigation of the nematosomes in the sea anemone Nematostella vectensis
BACKGROUND: The evolution of novel genes is thought to be a critical component of morphological innovation but few studies have explicitly examined the contribution of novel genes to the evolution of novel tissues. Nematosomes, the free-floating cellular masses that circulate through the body cavity...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877951/ https://www.ncbi.nlm.nih.gov/pubmed/27216622 http://dx.doi.org/10.1186/s12862-016-0683-3 |
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author | Babonis, Leslie S. Martindale, Mark Q. Ryan, Joseph F. |
author_facet | Babonis, Leslie S. Martindale, Mark Q. Ryan, Joseph F. |
author_sort | Babonis, Leslie S. |
collection | PubMed |
description | BACKGROUND: The evolution of novel genes is thought to be a critical component of morphological innovation but few studies have explicitly examined the contribution of novel genes to the evolution of novel tissues. Nematosomes, the free-floating cellular masses that circulate through the body cavity of the sea anemone Nematostella vectensis, are the defining apomorphy of the genus Nematostella and are a useful model for understanding the evolution of novel tissues. Although many hypotheses have been proposed, the function of nematosomes is unknown. To gain insight into their putative function and to test hypotheses about the role of lineage-specific genes in the evolution of novel structures, we have re-examined the cellular and molecular biology of nematosomes. RESULTS: Using behavioral assays, we demonstrate that nematosomes are capable of immobilizing live brine shrimp (Artemia salina) by discharging their abundant cnidocytes. Additionally, the ability of nematosomes to engulf fluorescently labeled bacteria (E. coli) reveals the presence of phagocytes in this tissue. Using RNA-Seq, we show that the gene expression profile of nematosomes is distinct from that of the tentacles and the mesenteries (their tissue of origin) and, further, that nematosomes (a Nematostella-specific tissue) are enriched in Nematostella-specific genes. CONCLUSIONS: Despite the small number of cell types they contain, nematosomes are distinct among tissues, both functionally and molecularly. We provide the first evidence that nematosomes comprise part of the innate immune system in N. vectensis, and suggest that this tissue is potentially an important place to look for genes associated with pathogen stress. Finally, we demonstrate that Nematostella-specific genes comprise a significant proportion of the differentially expressed genes in all three of the tissues we examined and may play an important role in novel cell functions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0683-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4877951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48779512016-05-25 Do novel genes drive morphological novelty? An investigation of the nematosomes in the sea anemone Nematostella vectensis Babonis, Leslie S. Martindale, Mark Q. Ryan, Joseph F. BMC Evol Biol Research Article BACKGROUND: The evolution of novel genes is thought to be a critical component of morphological innovation but few studies have explicitly examined the contribution of novel genes to the evolution of novel tissues. Nematosomes, the free-floating cellular masses that circulate through the body cavity of the sea anemone Nematostella vectensis, are the defining apomorphy of the genus Nematostella and are a useful model for understanding the evolution of novel tissues. Although many hypotheses have been proposed, the function of nematosomes is unknown. To gain insight into their putative function and to test hypotheses about the role of lineage-specific genes in the evolution of novel structures, we have re-examined the cellular and molecular biology of nematosomes. RESULTS: Using behavioral assays, we demonstrate that nematosomes are capable of immobilizing live brine shrimp (Artemia salina) by discharging their abundant cnidocytes. Additionally, the ability of nematosomes to engulf fluorescently labeled bacteria (E. coli) reveals the presence of phagocytes in this tissue. Using RNA-Seq, we show that the gene expression profile of nematosomes is distinct from that of the tentacles and the mesenteries (their tissue of origin) and, further, that nematosomes (a Nematostella-specific tissue) are enriched in Nematostella-specific genes. CONCLUSIONS: Despite the small number of cell types they contain, nematosomes are distinct among tissues, both functionally and molecularly. We provide the first evidence that nematosomes comprise part of the innate immune system in N. vectensis, and suggest that this tissue is potentially an important place to look for genes associated with pathogen stress. Finally, we demonstrate that Nematostella-specific genes comprise a significant proportion of the differentially expressed genes in all three of the tissues we examined and may play an important role in novel cell functions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0683-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-23 /pmc/articles/PMC4877951/ /pubmed/27216622 http://dx.doi.org/10.1186/s12862-016-0683-3 Text en © Babonis et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Babonis, Leslie S. Martindale, Mark Q. Ryan, Joseph F. Do novel genes drive morphological novelty? An investigation of the nematosomes in the sea anemone Nematostella vectensis |
title | Do novel genes drive morphological novelty? An investigation of the nematosomes in the sea anemone Nematostella vectensis |
title_full | Do novel genes drive morphological novelty? An investigation of the nematosomes in the sea anemone Nematostella vectensis |
title_fullStr | Do novel genes drive morphological novelty? An investigation of the nematosomes in the sea anemone Nematostella vectensis |
title_full_unstemmed | Do novel genes drive morphological novelty? An investigation of the nematosomes in the sea anemone Nematostella vectensis |
title_short | Do novel genes drive morphological novelty? An investigation of the nematosomes in the sea anemone Nematostella vectensis |
title_sort | do novel genes drive morphological novelty? an investigation of the nematosomes in the sea anemone nematostella vectensis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877951/ https://www.ncbi.nlm.nih.gov/pubmed/27216622 http://dx.doi.org/10.1186/s12862-016-0683-3 |
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