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CRISPR/Cas9‐based functional analysis of yellow gene in the diamondback moth, Plutella xylostella

The diamondback moth, Plutella xylostella (L.), is an economically important pest of cruciferous crops worldwide. This pest is notorious for rapid evolution of the resistance to different classes of insecticides, making it increasingly difficult to control. Genetics‐based control approaches, through...

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Autores principales: Wang, Yajun, Huang, Yuping, Xu, Xuejiao, Liu, Zhaoxia, Li, Jianyu, Zhan, Xue, Yang, Guang, You, Minsheng, You, Shijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518405/
https://www.ncbi.nlm.nih.gov/pubmed/32893952
http://dx.doi.org/10.1111/1744-7917.12870
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author Wang, Yajun
Huang, Yuping
Xu, Xuejiao
Liu, Zhaoxia
Li, Jianyu
Zhan, Xue
Yang, Guang
You, Minsheng
You, Shijun
author_facet Wang, Yajun
Huang, Yuping
Xu, Xuejiao
Liu, Zhaoxia
Li, Jianyu
Zhan, Xue
Yang, Guang
You, Minsheng
You, Shijun
author_sort Wang, Yajun
collection PubMed
description The diamondback moth, Plutella xylostella (L.), is an economically important pest of cruciferous crops worldwide. This pest is notorious for rapid evolution of the resistance to different classes of insecticides, making it increasingly difficult to control. Genetics‐based control approaches, through manipulation of target genes, have been reported as promising supplements or alternatives to traditional methods of pest management. Here we identified a gene of pigmentation (yellow) in P. xylostella, Pxyellow, which encodes 1674 bp complementary DNA sequence with four exons and three introns. Using the clustered regularly interspersed palindromic repeats (CRISPR)/CRISPR‐associated protein 9 system, we knocked out Pxyellow, targeting two sites in Exon III, to generate 272 chimeric mutants (57% of the CRISPR‐treated individuals) with color‐changed phenotypes of the 1st to 3rd instar larvae, pupae, and adults, indicating that Pxyellow plays an essential role in the body pigmentation of P. xylostella. Fitness analysis revealed no significant difference in the oviposition of adults, the hatchability of eggs, and the weight of pupae between homozygous mutants and wildtypes, suggesting that Pxyellow is not directly involved in regulation of growth, development, or reproduction. This work advances our understanding of the genetic and insect science molecular basis for body pigmentation of P. xylostella, and opens a wide avenue for development of the genetically based pest control techniques using Pxyellow as a screening marker.
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spelling pubmed-85184052021-10-21 CRISPR/Cas9‐based functional analysis of yellow gene in the diamondback moth, Plutella xylostella Wang, Yajun Huang, Yuping Xu, Xuejiao Liu, Zhaoxia Li, Jianyu Zhan, Xue Yang, Guang You, Minsheng You, Shijun Insect Sci Letter to the Editor The diamondback moth, Plutella xylostella (L.), is an economically important pest of cruciferous crops worldwide. This pest is notorious for rapid evolution of the resistance to different classes of insecticides, making it increasingly difficult to control. Genetics‐based control approaches, through manipulation of target genes, have been reported as promising supplements or alternatives to traditional methods of pest management. Here we identified a gene of pigmentation (yellow) in P. xylostella, Pxyellow, which encodes 1674 bp complementary DNA sequence with four exons and three introns. Using the clustered regularly interspersed palindromic repeats (CRISPR)/CRISPR‐associated protein 9 system, we knocked out Pxyellow, targeting two sites in Exon III, to generate 272 chimeric mutants (57% of the CRISPR‐treated individuals) with color‐changed phenotypes of the 1st to 3rd instar larvae, pupae, and adults, indicating that Pxyellow plays an essential role in the body pigmentation of P. xylostella. Fitness analysis revealed no significant difference in the oviposition of adults, the hatchability of eggs, and the weight of pupae between homozygous mutants and wildtypes, suggesting that Pxyellow is not directly involved in regulation of growth, development, or reproduction. This work advances our understanding of the genetic and insect science molecular basis for body pigmentation of P. xylostella, and opens a wide avenue for development of the genetically based pest control techniques using Pxyellow as a screening marker. John Wiley and Sons Inc. 2020-09-18 2021-10 /pmc/articles/PMC8518405/ /pubmed/32893952 http://dx.doi.org/10.1111/1744-7917.12870 Text en © 2020 The Authors. Insect Science published by John Wiley & Sons Australia, Ltd on behalf of Institute of Zoology, Chinese Academy of Sciences https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to the Editor
Wang, Yajun
Huang, Yuping
Xu, Xuejiao
Liu, Zhaoxia
Li, Jianyu
Zhan, Xue
Yang, Guang
You, Minsheng
You, Shijun
CRISPR/Cas9‐based functional analysis of yellow gene in the diamondback moth, Plutella xylostella
title CRISPR/Cas9‐based functional analysis of yellow gene in the diamondback moth, Plutella xylostella
title_full CRISPR/Cas9‐based functional analysis of yellow gene in the diamondback moth, Plutella xylostella
title_fullStr CRISPR/Cas9‐based functional analysis of yellow gene in the diamondback moth, Plutella xylostella
title_full_unstemmed CRISPR/Cas9‐based functional analysis of yellow gene in the diamondback moth, Plutella xylostella
title_short CRISPR/Cas9‐based functional analysis of yellow gene in the diamondback moth, Plutella xylostella
title_sort crispr/cas9‐based functional analysis of yellow gene in the diamondback moth, plutella xylostella
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518405/
https://www.ncbi.nlm.nih.gov/pubmed/32893952
http://dx.doi.org/10.1111/1744-7917.12870
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