Cargando…
The genomic architecture and molecular evolution of ant odorant receptors
The massive expansions of odorant receptor (OR) genes in ant genomes are notable examples of rapid genome evolution and adaptive gene duplication. However, the molecular mechanisms leading to gene family expansion remain poorly understood, partly because available ant genomes are fragmentary. Here,...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211649/ https://www.ncbi.nlm.nih.gov/pubmed/30249741 http://dx.doi.org/10.1101/gr.237123.118 |
_version_ | 1783367377587535872 |
---|---|
author | McKenzie, Sean K. Kronauer, Daniel J.C. |
author_facet | McKenzie, Sean K. Kronauer, Daniel J.C. |
author_sort | McKenzie, Sean K. |
collection | PubMed |
description | The massive expansions of odorant receptor (OR) genes in ant genomes are notable examples of rapid genome evolution and adaptive gene duplication. However, the molecular mechanisms leading to gene family expansion remain poorly understood, partly because available ant genomes are fragmentary. Here, we present a highly contiguous, chromosome-level assembly of the clonal raider ant genome, revealing the largest known OR repertoire in an insect. While most ant ORs originate via local tandem duplication, we also observe several cases of dispersed duplication followed by tandem duplication in the most rapidly evolving OR clades. We found that areas of unusually high transposable element density (TE islands) were depauperate in ORs in the clonal raider ant, and found no evidence for retrotransposition of ORs. However, OR loci were enriched for transposons relative to the genome as a whole, potentially facilitating tandem duplication by unequal crossing over. We also found that ant OR genes are highly AT-rich compared to other genes. In contrast, in flies, OR genes are dispersed and largely isolated within the genome, and we find that fly ORs are not AT-rich. The genomic architecture and composition of ant ORs thus show convergence with the unrelated vertebrate ORs rather than the related fly ORs. This might be related to the greater gene numbers and/or potential similarities in gene regulation between ants and vertebrates as compared to flies. |
format | Online Article Text |
id | pubmed-6211649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62116492019-05-01 The genomic architecture and molecular evolution of ant odorant receptors McKenzie, Sean K. Kronauer, Daniel J.C. Genome Res Resource The massive expansions of odorant receptor (OR) genes in ant genomes are notable examples of rapid genome evolution and adaptive gene duplication. However, the molecular mechanisms leading to gene family expansion remain poorly understood, partly because available ant genomes are fragmentary. Here, we present a highly contiguous, chromosome-level assembly of the clonal raider ant genome, revealing the largest known OR repertoire in an insect. While most ant ORs originate via local tandem duplication, we also observe several cases of dispersed duplication followed by tandem duplication in the most rapidly evolving OR clades. We found that areas of unusually high transposable element density (TE islands) were depauperate in ORs in the clonal raider ant, and found no evidence for retrotransposition of ORs. However, OR loci were enriched for transposons relative to the genome as a whole, potentially facilitating tandem duplication by unequal crossing over. We also found that ant OR genes are highly AT-rich compared to other genes. In contrast, in flies, OR genes are dispersed and largely isolated within the genome, and we find that fly ORs are not AT-rich. The genomic architecture and composition of ant ORs thus show convergence with the unrelated vertebrate ORs rather than the related fly ORs. This might be related to the greater gene numbers and/or potential similarities in gene regulation between ants and vertebrates as compared to flies. Cold Spring Harbor Laboratory Press 2018-11 /pmc/articles/PMC6211649/ /pubmed/30249741 http://dx.doi.org/10.1101/gr.237123.118 Text en © 2018 McKenzie and Kronauer; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Resource McKenzie, Sean K. Kronauer, Daniel J.C. The genomic architecture and molecular evolution of ant odorant receptors |
title | The genomic architecture and molecular evolution of ant odorant receptors |
title_full | The genomic architecture and molecular evolution of ant odorant receptors |
title_fullStr | The genomic architecture and molecular evolution of ant odorant receptors |
title_full_unstemmed | The genomic architecture and molecular evolution of ant odorant receptors |
title_short | The genomic architecture and molecular evolution of ant odorant receptors |
title_sort | genomic architecture and molecular evolution of ant odorant receptors |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211649/ https://www.ncbi.nlm.nih.gov/pubmed/30249741 http://dx.doi.org/10.1101/gr.237123.118 |
work_keys_str_mv | AT mckenzieseank thegenomicarchitectureandmolecularevolutionofantodorantreceptors AT kronauerdanieljc thegenomicarchitectureandmolecularevolutionofantodorantreceptors AT mckenzieseank genomicarchitectureandmolecularevolutionofantodorantreceptors AT kronauerdanieljc genomicarchitectureandmolecularevolutionofantodorantreceptors |