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Neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, Nilaparvata lugens

A single insulin receptor (InR) gene has been identified and extensively studied in model species ranging from nematodes to mice. However, most insects possess additional copies of InR, yet the functional significance, if any, of alternate InRs is unknown. Here, we used the wing-dimorphic brown plan...

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Autores principales: Xue, Wen-Hua, Xu, Nan, Chen, Sun-Jie, Liu, Xin-Yang, Zhang, Jin-Li, Xu, Hai-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270448/
https://www.ncbi.nlm.nih.gov/pubmed/34181658
http://dx.doi.org/10.1371/journal.pgen.1009653
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author Xue, Wen-Hua
Xu, Nan
Chen, Sun-Jie
Liu, Xin-Yang
Zhang, Jin-Li
Xu, Hai-Jun
author_facet Xue, Wen-Hua
Xu, Nan
Chen, Sun-Jie
Liu, Xin-Yang
Zhang, Jin-Li
Xu, Hai-Jun
author_sort Xue, Wen-Hua
collection PubMed
description A single insulin receptor (InR) gene has been identified and extensively studied in model species ranging from nematodes to mice. However, most insects possess additional copies of InR, yet the functional significance, if any, of alternate InRs is unknown. Here, we used the wing-dimorphic brown planthopper (BPH) as a model system to query the role of a second InR copy in insects. NlInR2 resembled the BPH InR homologue (NlInR1) in terms of nymph development and reproduction, but revealed distinct regulatory roles in fuel metabolism, lifespan, and starvation tolerance. Unlike a lethal phenotype derived from NlInR1 null, homozygous NlInR2 null mutants were viable and accelerated DNA replication and cell proliferation in wing cells, thus redirecting short-winged–destined BPHs to develop into long-winged morphs. Additionally, the proper expression of NlInR2 was needed to maintain symmetric vein patterning in wings. Our findings provide the first direct evidence for the regulatory complexity of the two InR paralogues in insects, implying the functionally independent evolution of multiple InRs in invertebrates.
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spelling pubmed-82704482021-07-21 Neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, Nilaparvata lugens Xue, Wen-Hua Xu, Nan Chen, Sun-Jie Liu, Xin-Yang Zhang, Jin-Li Xu, Hai-Jun PLoS Genet Research Article A single insulin receptor (InR) gene has been identified and extensively studied in model species ranging from nematodes to mice. However, most insects possess additional copies of InR, yet the functional significance, if any, of alternate InRs is unknown. Here, we used the wing-dimorphic brown planthopper (BPH) as a model system to query the role of a second InR copy in insects. NlInR2 resembled the BPH InR homologue (NlInR1) in terms of nymph development and reproduction, but revealed distinct regulatory roles in fuel metabolism, lifespan, and starvation tolerance. Unlike a lethal phenotype derived from NlInR1 null, homozygous NlInR2 null mutants were viable and accelerated DNA replication and cell proliferation in wing cells, thus redirecting short-winged–destined BPHs to develop into long-winged morphs. Additionally, the proper expression of NlInR2 was needed to maintain symmetric vein patterning in wings. Our findings provide the first direct evidence for the regulatory complexity of the two InR paralogues in insects, implying the functionally independent evolution of multiple InRs in invertebrates. Public Library of Science 2021-06-28 /pmc/articles/PMC8270448/ /pubmed/34181658 http://dx.doi.org/10.1371/journal.pgen.1009653 Text en © 2021 Xue et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Xue, Wen-Hua
Xu, Nan
Chen, Sun-Jie
Liu, Xin-Yang
Zhang, Jin-Li
Xu, Hai-Jun
Neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, Nilaparvata lugens
title Neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, Nilaparvata lugens
title_full Neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, Nilaparvata lugens
title_fullStr Neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, Nilaparvata lugens
title_full_unstemmed Neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, Nilaparvata lugens
title_short Neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, Nilaparvata lugens
title_sort neofunctionalization of a second insulin receptor gene in the wing-dimorphic planthopper, nilaparvata lugens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270448/
https://www.ncbi.nlm.nih.gov/pubmed/34181658
http://dx.doi.org/10.1371/journal.pgen.1009653
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