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Paralog analyses reveal gene duplication events and genes under positive selection in Ixodes scapularis and other ixodid ticks

BACKGROUND: Hard ticks (family Ixodidae) are obligatory hematophagous ectoparasites of worldwide medical and veterinary importance. The haploid genomes of multiple species of ixodid ticks exceed 1 Gbp, prompting questions regarding gene, segmental and whole genome duplication in this phyletic group....

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Autores principales: Van Zee, Janice P., Schlueter, Jessica A., Schlueter, Shannon, Dixon, Philip, Sierra, Carlos A. Brito, Hill, Catherine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793754/
https://www.ncbi.nlm.nih.gov/pubmed/26984180
http://dx.doi.org/10.1186/s12864-015-2350-2
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author Van Zee, Janice P.
Schlueter, Jessica A.
Schlueter, Shannon
Dixon, Philip
Sierra, Carlos A. Brito
Hill, Catherine A.
author_facet Van Zee, Janice P.
Schlueter, Jessica A.
Schlueter, Shannon
Dixon, Philip
Sierra, Carlos A. Brito
Hill, Catherine A.
author_sort Van Zee, Janice P.
collection PubMed
description BACKGROUND: Hard ticks (family Ixodidae) are obligatory hematophagous ectoparasites of worldwide medical and veterinary importance. The haploid genomes of multiple species of ixodid ticks exceed 1 Gbp, prompting questions regarding gene, segmental and whole genome duplication in this phyletic group. The availability of the genome assembly for the black legged tick, Ixodes scapularis, and transcriptome datasets for multiple species of ticks offers an opportunity to assess the contribution of gene duplication to the genome. Here we developed a bioinformatics pipeline to identify and analyze duplicated genes (paralogs) using gene models from the prostriate tick, I. scapularis IscaW1.1 annotation and expressed sequence tags (ESTs) from I. scapularis and the metastriate ticks, Rhipicephalus microplus (southern cattle tick), R. appendiculatus (brown ear tick) and Amblyomma variegatum (tropical bont tick). RESULTS: Approximately 1-2 % of I. scapularis gene models and 2-14 % of ESTs from the four species represent duplicated genes. The ratio of non-synonymous to synonymous nucleotide substitution rates suggests ~ 25 % of duplicated genes are under positive selection pressure in each species. Analyses of synonymous substitution rates provide evidence for two duplication events in I. scapularis and R. microplus involving several hundred genes. Conservative molecular clock estimates based on synonymous substitution rates for species of Anopheles mosquitoes and the fruit fly, Drosophila melanogaster, suggest these events occurred within the last 50 MYA. Mapping of paralogs to the I. scapularis genome assembly supports tandem, or possibly segmental duplication events. CONCLUSIONS: The present study marks the first genome-level analyses of gene duplication for the Ixodidae and provides insights into mechanisms shaping genome evolution in this group. At least two duplication events involving hundreds of genes may have occurred independently in the lineages prostriata and metastriata, with tandem and segmental duplication the most likely mechanisms for paralog generation. Duplicated genes under positive selection pressure may be linked to emerging functions in the tick and represent important candidates for further study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2350-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-47937542016-03-17 Paralog analyses reveal gene duplication events and genes under positive selection in Ixodes scapularis and other ixodid ticks Van Zee, Janice P. Schlueter, Jessica A. Schlueter, Shannon Dixon, Philip Sierra, Carlos A. Brito Hill, Catherine A. BMC Genomics Research Article BACKGROUND: Hard ticks (family Ixodidae) are obligatory hematophagous ectoparasites of worldwide medical and veterinary importance. The haploid genomes of multiple species of ixodid ticks exceed 1 Gbp, prompting questions regarding gene, segmental and whole genome duplication in this phyletic group. The availability of the genome assembly for the black legged tick, Ixodes scapularis, and transcriptome datasets for multiple species of ticks offers an opportunity to assess the contribution of gene duplication to the genome. Here we developed a bioinformatics pipeline to identify and analyze duplicated genes (paralogs) using gene models from the prostriate tick, I. scapularis IscaW1.1 annotation and expressed sequence tags (ESTs) from I. scapularis and the metastriate ticks, Rhipicephalus microplus (southern cattle tick), R. appendiculatus (brown ear tick) and Amblyomma variegatum (tropical bont tick). RESULTS: Approximately 1-2 % of I. scapularis gene models and 2-14 % of ESTs from the four species represent duplicated genes. The ratio of non-synonymous to synonymous nucleotide substitution rates suggests ~ 25 % of duplicated genes are under positive selection pressure in each species. Analyses of synonymous substitution rates provide evidence for two duplication events in I. scapularis and R. microplus involving several hundred genes. Conservative molecular clock estimates based on synonymous substitution rates for species of Anopheles mosquitoes and the fruit fly, Drosophila melanogaster, suggest these events occurred within the last 50 MYA. Mapping of paralogs to the I. scapularis genome assembly supports tandem, or possibly segmental duplication events. CONCLUSIONS: The present study marks the first genome-level analyses of gene duplication for the Ixodidae and provides insights into mechanisms shaping genome evolution in this group. At least two duplication events involving hundreds of genes may have occurred independently in the lineages prostriata and metastriata, with tandem and segmental duplication the most likely mechanisms for paralog generation. Duplicated genes under positive selection pressure may be linked to emerging functions in the tick and represent important candidates for further study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2350-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-16 /pmc/articles/PMC4793754/ /pubmed/26984180 http://dx.doi.org/10.1186/s12864-015-2350-2 Text en © Van Zee et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Van Zee, Janice P.
Schlueter, Jessica A.
Schlueter, Shannon
Dixon, Philip
Sierra, Carlos A. Brito
Hill, Catherine A.
Paralog analyses reveal gene duplication events and genes under positive selection in Ixodes scapularis and other ixodid ticks
title Paralog analyses reveal gene duplication events and genes under positive selection in Ixodes scapularis and other ixodid ticks
title_full Paralog analyses reveal gene duplication events and genes under positive selection in Ixodes scapularis and other ixodid ticks
title_fullStr Paralog analyses reveal gene duplication events and genes under positive selection in Ixodes scapularis and other ixodid ticks
title_full_unstemmed Paralog analyses reveal gene duplication events and genes under positive selection in Ixodes scapularis and other ixodid ticks
title_short Paralog analyses reveal gene duplication events and genes under positive selection in Ixodes scapularis and other ixodid ticks
title_sort paralog analyses reveal gene duplication events and genes under positive selection in ixodes scapularis and other ixodid ticks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793754/
https://www.ncbi.nlm.nih.gov/pubmed/26984180
http://dx.doi.org/10.1186/s12864-015-2350-2
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