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Mandarin fish (Sinipercidae) genomes provide insights into innate predatory feeding
Mandarin fishes (Sinipercidae) are piscivores that feed solely on live fry. Unlike higher vertebrates, teleosts exhibit feeding behavior driven mainly by genetic responses, with no modification by learning from parents. Mandarin fishes could serve as excellent model organisms for studying feeding be...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347838/ https://www.ncbi.nlm.nih.gov/pubmed/32647268 http://dx.doi.org/10.1038/s42003-020-1094-y |
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author | He, Shan Li, Ling Lv, Li-Yuan Cai, Wen-Jing Dou, Ya-Qi Li, Jiao Tang, Shu-Lin Chen, Xu Zhang, Zhen Xu, Jing Zhang, Yan-Peng Yin, Zhan Wuertz, Sven Tao, Ya-Xiong Kuhl, Heiner Liang, Xu-Fang |
author_facet | He, Shan Li, Ling Lv, Li-Yuan Cai, Wen-Jing Dou, Ya-Qi Li, Jiao Tang, Shu-Lin Chen, Xu Zhang, Zhen Xu, Jing Zhang, Yan-Peng Yin, Zhan Wuertz, Sven Tao, Ya-Xiong Kuhl, Heiner Liang, Xu-Fang |
author_sort | He, Shan |
collection | PubMed |
description | Mandarin fishes (Sinipercidae) are piscivores that feed solely on live fry. Unlike higher vertebrates, teleosts exhibit feeding behavior driven mainly by genetic responses, with no modification by learning from parents. Mandarin fishes could serve as excellent model organisms for studying feeding behavior. We report a long-read, chromosomal-scale genome assembly for Siniperca chuatsi and genome assemblies for Siniperca kneri, Siniperca scherzeri and Coreoperca whiteheadi. Positive selection analysis revealed rapid adaptive evolution of genes related to predatory feeding/aggression, growth, pyloric caeca and euryhalinity. Very few gill rakers are observed in mandarin fishes; analogously, we found that zebrafish deficient in edar had a gill raker loss phenotype and a more predatory habit, with reduced intake of zooplankton but increased intake of prey fish. Higher expression of bmp4, which could inhibit edar expression and gill raker development through binding of a Xvent-1 site upstream of edar, may cause predatory feeding in Siniperca. |
format | Online Article Text |
id | pubmed-7347838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73478382020-07-13 Mandarin fish (Sinipercidae) genomes provide insights into innate predatory feeding He, Shan Li, Ling Lv, Li-Yuan Cai, Wen-Jing Dou, Ya-Qi Li, Jiao Tang, Shu-Lin Chen, Xu Zhang, Zhen Xu, Jing Zhang, Yan-Peng Yin, Zhan Wuertz, Sven Tao, Ya-Xiong Kuhl, Heiner Liang, Xu-Fang Commun Biol Article Mandarin fishes (Sinipercidae) are piscivores that feed solely on live fry. Unlike higher vertebrates, teleosts exhibit feeding behavior driven mainly by genetic responses, with no modification by learning from parents. Mandarin fishes could serve as excellent model organisms for studying feeding behavior. We report a long-read, chromosomal-scale genome assembly for Siniperca chuatsi and genome assemblies for Siniperca kneri, Siniperca scherzeri and Coreoperca whiteheadi. Positive selection analysis revealed rapid adaptive evolution of genes related to predatory feeding/aggression, growth, pyloric caeca and euryhalinity. Very few gill rakers are observed in mandarin fishes; analogously, we found that zebrafish deficient in edar had a gill raker loss phenotype and a more predatory habit, with reduced intake of zooplankton but increased intake of prey fish. Higher expression of bmp4, which could inhibit edar expression and gill raker development through binding of a Xvent-1 site upstream of edar, may cause predatory feeding in Siniperca. Nature Publishing Group UK 2020-07-09 /pmc/articles/PMC7347838/ /pubmed/32647268 http://dx.doi.org/10.1038/s42003-020-1094-y Text en © The Author(s) 2020 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/. |
spellingShingle | Article He, Shan Li, Ling Lv, Li-Yuan Cai, Wen-Jing Dou, Ya-Qi Li, Jiao Tang, Shu-Lin Chen, Xu Zhang, Zhen Xu, Jing Zhang, Yan-Peng Yin, Zhan Wuertz, Sven Tao, Ya-Xiong Kuhl, Heiner Liang, Xu-Fang Mandarin fish (Sinipercidae) genomes provide insights into innate predatory feeding |
title | Mandarin fish (Sinipercidae) genomes provide insights into innate predatory feeding |
title_full | Mandarin fish (Sinipercidae) genomes provide insights into innate predatory feeding |
title_fullStr | Mandarin fish (Sinipercidae) genomes provide insights into innate predatory feeding |
title_full_unstemmed | Mandarin fish (Sinipercidae) genomes provide insights into innate predatory feeding |
title_short | Mandarin fish (Sinipercidae) genomes provide insights into innate predatory feeding |
title_sort | mandarin fish (sinipercidae) genomes provide insights into innate predatory feeding |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347838/ https://www.ncbi.nlm.nih.gov/pubmed/32647268 http://dx.doi.org/10.1038/s42003-020-1094-y |
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