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Chromosome-level genome assembly of Bactrocera dorsalis reveals its adaptation and invasion mechanisms
Bactrocera dorsalis is an invasive polyphagous pest causing considerable ecological and economic damage worldwide. We report a high-quality chromosome-level genome assembly and combine various transcriptome data to explore the molecular mechanisms of its rapid adaptation to new environments. The exp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752857/ https://www.ncbi.nlm.nih.gov/pubmed/35017661 http://dx.doi.org/10.1038/s42003-021-02966-6 |
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author | Jiang, Fan Liang, Liang Wang, Jing Zhu, Shuifang |
author_facet | Jiang, Fan Liang, Liang Wang, Jing Zhu, Shuifang |
author_sort | Jiang, Fan |
collection | PubMed |
description | Bactrocera dorsalis is an invasive polyphagous pest causing considerable ecological and economic damage worldwide. We report a high-quality chromosome-level genome assembly and combine various transcriptome data to explore the molecular mechanisms of its rapid adaptation to new environments. The expansions of the DDE transposase superfamily and key gene families related to environmental adaptation and enrichment of the expanded and unique gene families in metabolism and defence response pathways explain its environmental adaptability. The relatively high but not significantly different expression of heat-shock proteins, regardless of the environmental conditions, suggests an intrinsic mechanism underlying its adaptation to high temperatures. The mitogen-activated protein kinase pathway plays a key role in adaptation to new environments. The prevalence of duplicated genes in its genome explains the diversity in the B. dorsalis complex. These findings provide insights into the genetic basis of the invasiveness and diversity of B. dorsalis, explaining its rapid adaptation and expansion. |
format | Online Article Text |
id | pubmed-8752857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87528572022-01-20 Chromosome-level genome assembly of Bactrocera dorsalis reveals its adaptation and invasion mechanisms Jiang, Fan Liang, Liang Wang, Jing Zhu, Shuifang Commun Biol Article Bactrocera dorsalis is an invasive polyphagous pest causing considerable ecological and economic damage worldwide. We report a high-quality chromosome-level genome assembly and combine various transcriptome data to explore the molecular mechanisms of its rapid adaptation to new environments. The expansions of the DDE transposase superfamily and key gene families related to environmental adaptation and enrichment of the expanded and unique gene families in metabolism and defence response pathways explain its environmental adaptability. The relatively high but not significantly different expression of heat-shock proteins, regardless of the environmental conditions, suggests an intrinsic mechanism underlying its adaptation to high temperatures. The mitogen-activated protein kinase pathway plays a key role in adaptation to new environments. The prevalence of duplicated genes in its genome explains the diversity in the B. dorsalis complex. These findings provide insights into the genetic basis of the invasiveness and diversity of B. dorsalis, explaining its rapid adaptation and expansion. Nature Publishing Group UK 2022-01-11 /pmc/articles/PMC8752857/ /pubmed/35017661 http://dx.doi.org/10.1038/s42003-021-02966-6 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jiang, Fan Liang, Liang Wang, Jing Zhu, Shuifang Chromosome-level genome assembly of Bactrocera dorsalis reveals its adaptation and invasion mechanisms |
title | Chromosome-level genome assembly of Bactrocera dorsalis reveals its adaptation and invasion mechanisms |
title_full | Chromosome-level genome assembly of Bactrocera dorsalis reveals its adaptation and invasion mechanisms |
title_fullStr | Chromosome-level genome assembly of Bactrocera dorsalis reveals its adaptation and invasion mechanisms |
title_full_unstemmed | Chromosome-level genome assembly of Bactrocera dorsalis reveals its adaptation and invasion mechanisms |
title_short | Chromosome-level genome assembly of Bactrocera dorsalis reveals its adaptation and invasion mechanisms |
title_sort | chromosome-level genome assembly of bactrocera dorsalis reveals its adaptation and invasion mechanisms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752857/ https://www.ncbi.nlm.nih.gov/pubmed/35017661 http://dx.doi.org/10.1038/s42003-021-02966-6 |
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