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Genome of the Parasitoid Wasp Diachasma alloeum, an Emerging Model for Ecological Speciation and Transitions to Asexual Reproduction

Parasitoid wasps are among the most speciose animals, yet have relatively few available genomic resources. We report a draft genome assembly of the wasp Diachasma alloeum (Hymenoptera: Braconidae), a host-specific parasitoid of the apple maggot fly Rhagoletis pomonella (Diptera: Tephritidae), and a...

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Autores principales: Tvedte, Eric S, Walden, Kimberly K O, McElroy, Kyle E, Werren, John H, Forbes, Andrew A, Hood, Glen R, Logsdon, John M, Feder, Jeffrey L, Robertson, Hugh M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781843/
https://www.ncbi.nlm.nih.gov/pubmed/31553440
http://dx.doi.org/10.1093/gbe/evz205
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author Tvedte, Eric S
Walden, Kimberly K O
McElroy, Kyle E
Werren, John H
Forbes, Andrew A
Hood, Glen R
Logsdon, John M
Feder, Jeffrey L
Robertson, Hugh M
author_facet Tvedte, Eric S
Walden, Kimberly K O
McElroy, Kyle E
Werren, John H
Forbes, Andrew A
Hood, Glen R
Logsdon, John M
Feder, Jeffrey L
Robertson, Hugh M
author_sort Tvedte, Eric S
collection PubMed
description Parasitoid wasps are among the most speciose animals, yet have relatively few available genomic resources. We report a draft genome assembly of the wasp Diachasma alloeum (Hymenoptera: Braconidae), a host-specific parasitoid of the apple maggot fly Rhagoletis pomonella (Diptera: Tephritidae), and a developing model for understanding how ecological speciation can “cascade” across trophic levels. Identification of gene content confirmed the overall quality of the draft genome, and we manually annotated ∼400 genes as part of this study, including those involved in oxidative phosphorylation, chemosensation, and reproduction. Through comparisons to model hymenopterans such as the European honeybee Apis mellifera and parasitoid wasp Nasonia vitripennis, as well as a more closely related braconid parasitoid Microplitis demolitor, we identified a proliferation of transposable elements in the genome, an expansion of chemosensory genes in parasitoid wasps, and the maintenance of several key genes with known roles in sexual reproduction and sex determination. The D. alloeum genome will provide a valuable resource for comparative genomics studies in Hymenoptera as well as specific investigations into the genomic changes associated with ecological speciation and transitions to asexuality.
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spelling pubmed-67818432019-10-18 Genome of the Parasitoid Wasp Diachasma alloeum, an Emerging Model for Ecological Speciation and Transitions to Asexual Reproduction Tvedte, Eric S Walden, Kimberly K O McElroy, Kyle E Werren, John H Forbes, Andrew A Hood, Glen R Logsdon, John M Feder, Jeffrey L Robertson, Hugh M Genome Biol Evol Genome Report Parasitoid wasps are among the most speciose animals, yet have relatively few available genomic resources. We report a draft genome assembly of the wasp Diachasma alloeum (Hymenoptera: Braconidae), a host-specific parasitoid of the apple maggot fly Rhagoletis pomonella (Diptera: Tephritidae), and a developing model for understanding how ecological speciation can “cascade” across trophic levels. Identification of gene content confirmed the overall quality of the draft genome, and we manually annotated ∼400 genes as part of this study, including those involved in oxidative phosphorylation, chemosensation, and reproduction. Through comparisons to model hymenopterans such as the European honeybee Apis mellifera and parasitoid wasp Nasonia vitripennis, as well as a more closely related braconid parasitoid Microplitis demolitor, we identified a proliferation of transposable elements in the genome, an expansion of chemosensory genes in parasitoid wasps, and the maintenance of several key genes with known roles in sexual reproduction and sex determination. The D. alloeum genome will provide a valuable resource for comparative genomics studies in Hymenoptera as well as specific investigations into the genomic changes associated with ecological speciation and transitions to asexuality. Oxford University Press 2019-09-25 /pmc/articles/PMC6781843/ /pubmed/31553440 http://dx.doi.org/10.1093/gbe/evz205 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Report
Tvedte, Eric S
Walden, Kimberly K O
McElroy, Kyle E
Werren, John H
Forbes, Andrew A
Hood, Glen R
Logsdon, John M
Feder, Jeffrey L
Robertson, Hugh M
Genome of the Parasitoid Wasp Diachasma alloeum, an Emerging Model for Ecological Speciation and Transitions to Asexual Reproduction
title Genome of the Parasitoid Wasp Diachasma alloeum, an Emerging Model for Ecological Speciation and Transitions to Asexual Reproduction
title_full Genome of the Parasitoid Wasp Diachasma alloeum, an Emerging Model for Ecological Speciation and Transitions to Asexual Reproduction
title_fullStr Genome of the Parasitoid Wasp Diachasma alloeum, an Emerging Model for Ecological Speciation and Transitions to Asexual Reproduction
title_full_unstemmed Genome of the Parasitoid Wasp Diachasma alloeum, an Emerging Model for Ecological Speciation and Transitions to Asexual Reproduction
title_short Genome of the Parasitoid Wasp Diachasma alloeum, an Emerging Model for Ecological Speciation and Transitions to Asexual Reproduction
title_sort genome of the parasitoid wasp diachasma alloeum, an emerging model for ecological speciation and transitions to asexual reproduction
topic Genome Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781843/
https://www.ncbi.nlm.nih.gov/pubmed/31553440
http://dx.doi.org/10.1093/gbe/evz205
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