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Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins

Plants have evolved sophisticated embryo defences by kinetically-stable non-digestible storage proteins that lower the nutritional value of seeds, a strategy that have not been reported in animals. To further understand antinutritive defences in animals, we analysed PmPV1, massively accumulated in t...

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Autores principales: Pasquevich, María Yanina, Dreon, Marcos Sebastián, Qiu, Jian-Wen, Mu, Huawei, Heras, Horacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696525/
https://www.ncbi.nlm.nih.gov/pubmed/29158565
http://dx.doi.org/10.1038/s41598-017-16185-9
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author Pasquevich, María Yanina
Dreon, Marcos Sebastián
Qiu, Jian-Wen
Mu, Huawei
Heras, Horacio
author_facet Pasquevich, María Yanina
Dreon, Marcos Sebastián
Qiu, Jian-Wen
Mu, Huawei
Heras, Horacio
author_sort Pasquevich, María Yanina
collection PubMed
description Plants have evolved sophisticated embryo defences by kinetically-stable non-digestible storage proteins that lower the nutritional value of seeds, a strategy that have not been reported in animals. To further understand antinutritive defences in animals, we analysed PmPV1, massively accumulated in the eggs of the gastropod Pomacea maculata, focusing on how its structure and structural stability features affected its capacity to withstand passage through predator guts. The native protein withstands >50 min boiling and resists the denaturing detergent sodium dodecyl sulphate (SDS), indicating an unusually high structural stability (i.e., kinetic stability). PmPV1 is highly resistant to in vitro proteinase digestion and displays structural stability between pH 2.0–12.0 and 25–85 °C. Furthermore, PmPV1 withstands in vitro and mice digestion and is recovered unchanged in faeces, supporting an antinutritive defensive function. Subunit sequence similarities suggest a common origin and tolerance to mutations. This is the first known animal genus that, like plant seeds, lowers the nutritional value of eggs by kinetically-stable non-digestible storage proteins that survive the gut of predators unaffected. The selective pressure of the harsh gastrointestinal environment would have favoured their appearance, extending by convergent evolution the presence of plant-like hyperstable antinutritive proteins to unattended reproductive stages in animals.
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spelling pubmed-56965252017-11-29 Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins Pasquevich, María Yanina Dreon, Marcos Sebastián Qiu, Jian-Wen Mu, Huawei Heras, Horacio Sci Rep Article Plants have evolved sophisticated embryo defences by kinetically-stable non-digestible storage proteins that lower the nutritional value of seeds, a strategy that have not been reported in animals. To further understand antinutritive defences in animals, we analysed PmPV1, massively accumulated in the eggs of the gastropod Pomacea maculata, focusing on how its structure and structural stability features affected its capacity to withstand passage through predator guts. The native protein withstands >50 min boiling and resists the denaturing detergent sodium dodecyl sulphate (SDS), indicating an unusually high structural stability (i.e., kinetic stability). PmPV1 is highly resistant to in vitro proteinase digestion and displays structural stability between pH 2.0–12.0 and 25–85 °C. Furthermore, PmPV1 withstands in vitro and mice digestion and is recovered unchanged in faeces, supporting an antinutritive defensive function. Subunit sequence similarities suggest a common origin and tolerance to mutations. This is the first known animal genus that, like plant seeds, lowers the nutritional value of eggs by kinetically-stable non-digestible storage proteins that survive the gut of predators unaffected. The selective pressure of the harsh gastrointestinal environment would have favoured their appearance, extending by convergent evolution the presence of plant-like hyperstable antinutritive proteins to unattended reproductive stages in animals. Nature Publishing Group UK 2017-11-20 /pmc/articles/PMC5696525/ /pubmed/29158565 http://dx.doi.org/10.1038/s41598-017-16185-9 Text en © The Author(s) 2017 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
Pasquevich, María Yanina
Dreon, Marcos Sebastián
Qiu, Jian-Wen
Mu, Huawei
Heras, Horacio
Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins
title Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins
title_full Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins
title_fullStr Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins
title_full_unstemmed Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins
title_short Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins
title_sort convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696525/
https://www.ncbi.nlm.nih.gov/pubmed/29158565
http://dx.doi.org/10.1038/s41598-017-16185-9
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