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Gene Family Evolution in the Pea Aphid Based on Chromosome-Level Genome Assembly

Genome structural variations, including duplications, deletions, insertions, and inversions, are central in the evolution of eukaryotic genomes. However, structural variations present challenges for high-quality genome assembly, hampering efforts to understand the evolution of gene families and geno...

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Autores principales: Li, Yiyuan, Park, Hyunjin, Smith, Thomas E, Moran, Nancy A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759078/
https://www.ncbi.nlm.nih.gov/pubmed/31173104
http://dx.doi.org/10.1093/molbev/msz138
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author Li, Yiyuan
Park, Hyunjin
Smith, Thomas E
Moran, Nancy A
author_facet Li, Yiyuan
Park, Hyunjin
Smith, Thomas E
Moran, Nancy A
author_sort Li, Yiyuan
collection PubMed
description Genome structural variations, including duplications, deletions, insertions, and inversions, are central in the evolution of eukaryotic genomes. However, structural variations present challenges for high-quality genome assembly, hampering efforts to understand the evolution of gene families and genome architecture. An example is the genome of the pea aphid (Acyrthosiphon pisum) for which the current assembly is composed of thousands of short scaffolds, many of which are known to be misassembled. Here, we present an improved version of the A. pisum genome based on the use of two long-range proximity ligation methods. The new assembly contains four long scaffolds (40–170 Mb), corresponding to the three autosomes and the X chromosome of A. pisum, and encompassing 86% of the new assembly. Assembly accuracy is supported by several quality assessments. Using this assembly, we identify the chromosomal locations and relative ages of duplication events, and the locations of horizontally acquired genes. The improved assembly illuminates the mode of gene family evolution by providing proximity information between paralogs. By estimating nucleotide polymorphism and coverage depth from resequencing data, we determined that many short scaffolds not assembling to chromosomes represent hemizygous regions, which are especially frequent on the highly repetitive X chromosome. Aligning the X-linked aphicarus region, responsible for male wing dimorphism, to the new assembly revealed a 50-kb deletion that cosegregates with the winged male phenotype in some clones. These results show that long-range scaffolding methods can substantially improve assemblies of repetitive genomes and facilitate study of gene family evolution and structural variation.
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spelling pubmed-67590782019-10-02 Gene Family Evolution in the Pea Aphid Based on Chromosome-Level Genome Assembly Li, Yiyuan Park, Hyunjin Smith, Thomas E Moran, Nancy A Mol Biol Evol Fast Track Genome structural variations, including duplications, deletions, insertions, and inversions, are central in the evolution of eukaryotic genomes. However, structural variations present challenges for high-quality genome assembly, hampering efforts to understand the evolution of gene families and genome architecture. An example is the genome of the pea aphid (Acyrthosiphon pisum) for which the current assembly is composed of thousands of short scaffolds, many of which are known to be misassembled. Here, we present an improved version of the A. pisum genome based on the use of two long-range proximity ligation methods. The new assembly contains four long scaffolds (40–170 Mb), corresponding to the three autosomes and the X chromosome of A. pisum, and encompassing 86% of the new assembly. Assembly accuracy is supported by several quality assessments. Using this assembly, we identify the chromosomal locations and relative ages of duplication events, and the locations of horizontally acquired genes. The improved assembly illuminates the mode of gene family evolution by providing proximity information between paralogs. By estimating nucleotide polymorphism and coverage depth from resequencing data, we determined that many short scaffolds not assembling to chromosomes represent hemizygous regions, which are especially frequent on the highly repetitive X chromosome. Aligning the X-linked aphicarus region, responsible for male wing dimorphism, to the new assembly revealed a 50-kb deletion that cosegregates with the winged male phenotype in some clones. These results show that long-range scaffolding methods can substantially improve assemblies of repetitive genomes and facilitate study of gene family evolution and structural variation. Oxford University Press 2019-10 2019-06-07 /pmc/articles/PMC6759078/ /pubmed/31173104 http://dx.doi.org/10.1093/molbev/msz138 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-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 Fast Track
Li, Yiyuan
Park, Hyunjin
Smith, Thomas E
Moran, Nancy A
Gene Family Evolution in the Pea Aphid Based on Chromosome-Level Genome Assembly
title Gene Family Evolution in the Pea Aphid Based on Chromosome-Level Genome Assembly
title_full Gene Family Evolution in the Pea Aphid Based on Chromosome-Level Genome Assembly
title_fullStr Gene Family Evolution in the Pea Aphid Based on Chromosome-Level Genome Assembly
title_full_unstemmed Gene Family Evolution in the Pea Aphid Based on Chromosome-Level Genome Assembly
title_short Gene Family Evolution in the Pea Aphid Based on Chromosome-Level Genome Assembly
title_sort gene family evolution in the pea aphid based on chromosome-level genome assembly
topic Fast Track
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759078/
https://www.ncbi.nlm.nih.gov/pubmed/31173104
http://dx.doi.org/10.1093/molbev/msz138
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