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Horizontally Transferred Salivary Protein Promotes Insect Feeding by Suppressing Ferredoxin-Mediated Plant Defenses
Herbivorous insects such as whiteflies, planthoppers, and aphids secrete abundant orphan proteins to facilitate feeding. Yet, how these genes are recruited and evolve to mediate plant–insect interaction remains unknown. In this study, we report a horizontal gene transfer (HGT) event from fungi to an...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583550/ https://www.ncbi.nlm.nih.gov/pubmed/37804524 http://dx.doi.org/10.1093/molbev/msad221 |
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author | Wang, Yi-Zhe Ye, Yu-Xuan Lu, Jia-Bao Wang, Xin Lu, Hai-Bin Zhang, Ze-Long Ye, Zhuang-Xin Lu, Yu-Wen Sun, Zong-Tao Chen, Jian-Ping Li, Jun-Min Zhang, Chuan-Xi Huang, Hai-Jian |
author_facet | Wang, Yi-Zhe Ye, Yu-Xuan Lu, Jia-Bao Wang, Xin Lu, Hai-Bin Zhang, Ze-Long Ye, Zhuang-Xin Lu, Yu-Wen Sun, Zong-Tao Chen, Jian-Ping Li, Jun-Min Zhang, Chuan-Xi Huang, Hai-Jian |
author_sort | Wang, Yi-Zhe |
collection | PubMed |
description | Herbivorous insects such as whiteflies, planthoppers, and aphids secrete abundant orphan proteins to facilitate feeding. Yet, how these genes are recruited and evolve to mediate plant–insect interaction remains unknown. In this study, we report a horizontal gene transfer (HGT) event from fungi to an ancestor of Aleyrodidae insects approximately 42 to 190 million years ago. BtFTSP1 is a salivary protein that is secreted into host plants during Bemisia tabaci feeding. It targets a defensive ferredoxin 1 in Nicotiana tabacum (NtFD1) and disrupts the NtFD1–NtFD1 interaction in plant cytosol, leading to the degradation of NtFD1 in a ubiquitin-dependent manner. Silencing BtFTSP1 has negative effects on B. tabaci feeding while overexpressing BtFTSP1 in N. tabacum benefits insects and rescues the adverse effect caused by NtFD1 overexpression. The association between BtFTSP1 and NtFD1 is newly evolved after HGT, with the homologous FTSP in its fungal donor failing to interact and destabilize NtFD1. Our study illustrates the important roles of horizontally transferred genes in plant–insect interactions and suggests the potential origin of orphan salivary genes. |
format | Online Article Text |
id | pubmed-10583550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105835502023-10-19 Horizontally Transferred Salivary Protein Promotes Insect Feeding by Suppressing Ferredoxin-Mediated Plant Defenses Wang, Yi-Zhe Ye, Yu-Xuan Lu, Jia-Bao Wang, Xin Lu, Hai-Bin Zhang, Ze-Long Ye, Zhuang-Xin Lu, Yu-Wen Sun, Zong-Tao Chen, Jian-Ping Li, Jun-Min Zhang, Chuan-Xi Huang, Hai-Jian Mol Biol Evol Discoveries Herbivorous insects such as whiteflies, planthoppers, and aphids secrete abundant orphan proteins to facilitate feeding. Yet, how these genes are recruited and evolve to mediate plant–insect interaction remains unknown. In this study, we report a horizontal gene transfer (HGT) event from fungi to an ancestor of Aleyrodidae insects approximately 42 to 190 million years ago. BtFTSP1 is a salivary protein that is secreted into host plants during Bemisia tabaci feeding. It targets a defensive ferredoxin 1 in Nicotiana tabacum (NtFD1) and disrupts the NtFD1–NtFD1 interaction in plant cytosol, leading to the degradation of NtFD1 in a ubiquitin-dependent manner. Silencing BtFTSP1 has negative effects on B. tabaci feeding while overexpressing BtFTSP1 in N. tabacum benefits insects and rescues the adverse effect caused by NtFD1 overexpression. The association between BtFTSP1 and NtFD1 is newly evolved after HGT, with the homologous FTSP in its fungal donor failing to interact and destabilize NtFD1. Our study illustrates the important roles of horizontally transferred genes in plant–insect interactions and suggests the potential origin of orphan salivary genes. Oxford University Press 2023-10-07 /pmc/articles/PMC10583550/ /pubmed/37804524 http://dx.doi.org/10.1093/molbev/msad221 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Wang, Yi-Zhe Ye, Yu-Xuan Lu, Jia-Bao Wang, Xin Lu, Hai-Bin Zhang, Ze-Long Ye, Zhuang-Xin Lu, Yu-Wen Sun, Zong-Tao Chen, Jian-Ping Li, Jun-Min Zhang, Chuan-Xi Huang, Hai-Jian Horizontally Transferred Salivary Protein Promotes Insect Feeding by Suppressing Ferredoxin-Mediated Plant Defenses |
title | Horizontally Transferred Salivary Protein Promotes Insect Feeding by Suppressing Ferredoxin-Mediated Plant Defenses |
title_full | Horizontally Transferred Salivary Protein Promotes Insect Feeding by Suppressing Ferredoxin-Mediated Plant Defenses |
title_fullStr | Horizontally Transferred Salivary Protein Promotes Insect Feeding by Suppressing Ferredoxin-Mediated Plant Defenses |
title_full_unstemmed | Horizontally Transferred Salivary Protein Promotes Insect Feeding by Suppressing Ferredoxin-Mediated Plant Defenses |
title_short | Horizontally Transferred Salivary Protein Promotes Insect Feeding by Suppressing Ferredoxin-Mediated Plant Defenses |
title_sort | horizontally transferred salivary protein promotes insect feeding by suppressing ferredoxin-mediated plant defenses |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583550/ https://www.ncbi.nlm.nih.gov/pubmed/37804524 http://dx.doi.org/10.1093/molbev/msad221 |
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