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Shared Transcriptional Control and Disparate Gain and Loss of Aphid Parasitism Genes

Aphids are a diverse group of taxa that contain agronomically important species, which vary in their host range and ability to infest crop plants. The genome evolution underlying agriculturally important aphid traits is not well understood. We generated draft genome assemblies for two aphid species:...

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Autores principales: Thorpe, Peter, Escudero-Martinez, Carmen M, Cock, Peter J A, Eves-van den Akker, Sebastian, Bos, Jorunn I B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186164/
https://www.ncbi.nlm.nih.gov/pubmed/30165560
http://dx.doi.org/10.1093/gbe/evy183
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author Thorpe, Peter
Escudero-Martinez, Carmen M
Cock, Peter J A
Eves-van den Akker, Sebastian
Bos, Jorunn I B
author_facet Thorpe, Peter
Escudero-Martinez, Carmen M
Cock, Peter J A
Eves-van den Akker, Sebastian
Bos, Jorunn I B
author_sort Thorpe, Peter
collection PubMed
description Aphids are a diverse group of taxa that contain agronomically important species, which vary in their host range and ability to infest crop plants. The genome evolution underlying agriculturally important aphid traits is not well understood. We generated draft genome assemblies for two aphid species: Myzus cerasi (black cherry aphid) and the cereal specialist Rhopalosiphum padi. Using a de novo gene prediction pipeline on both these, and three additional aphid genome assemblies (Acyrthosiphon pisum, Diuraphis noxia, and Myzus persicae), we show that aphid genomes consistently encode similar gene numbers. We compare gene content, gene duplication, synteny, and putative effector repertoires between these five species to understand the genome evolution of globally important plant parasites. Aphid genomes show signs of relatively distant gene duplication, and substantial, relatively recent, gene birth. Putative effector repertoires, originating from duplicated and other loci, have an unusual genomic organization and evolutionary history. We identify a highly conserved effector pair that is tightly physically linked in the genomes of all aphid species tested. In R. padi, this effector pair is tightly transcriptionally linked and shares an unknown transcriptional control mechanism with a subset of ∼50 other putative effectors and secretory proteins. This study extends our current knowledge on the evolution of aphid genomes and reveals evidence for an as-of-yet unknown shared control mechanism, which underlies effector expression, and ultimately plant parasitism.
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spelling pubmed-61861642018-10-18 Shared Transcriptional Control and Disparate Gain and Loss of Aphid Parasitism Genes Thorpe, Peter Escudero-Martinez, Carmen M Cock, Peter J A Eves-van den Akker, Sebastian Bos, Jorunn I B Genome Biol Evol Research Article Aphids are a diverse group of taxa that contain agronomically important species, which vary in their host range and ability to infest crop plants. The genome evolution underlying agriculturally important aphid traits is not well understood. We generated draft genome assemblies for two aphid species: Myzus cerasi (black cherry aphid) and the cereal specialist Rhopalosiphum padi. Using a de novo gene prediction pipeline on both these, and three additional aphid genome assemblies (Acyrthosiphon pisum, Diuraphis noxia, and Myzus persicae), we show that aphid genomes consistently encode similar gene numbers. We compare gene content, gene duplication, synteny, and putative effector repertoires between these five species to understand the genome evolution of globally important plant parasites. Aphid genomes show signs of relatively distant gene duplication, and substantial, relatively recent, gene birth. Putative effector repertoires, originating from duplicated and other loci, have an unusual genomic organization and evolutionary history. We identify a highly conserved effector pair that is tightly physically linked in the genomes of all aphid species tested. In R. padi, this effector pair is tightly transcriptionally linked and shares an unknown transcriptional control mechanism with a subset of ∼50 other putative effectors and secretory proteins. This study extends our current knowledge on the evolution of aphid genomes and reveals evidence for an as-of-yet unknown shared control mechanism, which underlies effector expression, and ultimately plant parasitism. Oxford University Press 2018-08-25 /pmc/articles/PMC6186164/ /pubmed/30165560 http://dx.doi.org/10.1093/gbe/evy183 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Thorpe, Peter
Escudero-Martinez, Carmen M
Cock, Peter J A
Eves-van den Akker, Sebastian
Bos, Jorunn I B
Shared Transcriptional Control and Disparate Gain and Loss of Aphid Parasitism Genes
title Shared Transcriptional Control and Disparate Gain and Loss of Aphid Parasitism Genes
title_full Shared Transcriptional Control and Disparate Gain and Loss of Aphid Parasitism Genes
title_fullStr Shared Transcriptional Control and Disparate Gain and Loss of Aphid Parasitism Genes
title_full_unstemmed Shared Transcriptional Control and Disparate Gain and Loss of Aphid Parasitism Genes
title_short Shared Transcriptional Control and Disparate Gain and Loss of Aphid Parasitism Genes
title_sort shared transcriptional control and disparate gain and loss of aphid parasitism genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186164/
https://www.ncbi.nlm.nih.gov/pubmed/30165560
http://dx.doi.org/10.1093/gbe/evy183
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