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The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters

BACKGROUND: We report the sequencing, assembly and analysis of the genome of the Komodo dragon (Varanus komodoensis), the largest extant lizard, with a focus on antimicrobial host-defense peptides. The Komodo dragon diet includes carrion, and a complex milieu of bacteria, including potentially patho...

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Autores principales: van Hoek, Monique L., Prickett, M. Dennis, Settlage, Robert E., Kang, Lin, Michalak, Pawel, Vliet, Kent A., Bishop, Barney M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716921/
https://www.ncbi.nlm.nih.gov/pubmed/31470795
http://dx.doi.org/10.1186/s12864-019-6029-y
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author van Hoek, Monique L.
Prickett, M. Dennis
Settlage, Robert E.
Kang, Lin
Michalak, Pawel
Vliet, Kent A.
Bishop, Barney M.
author_facet van Hoek, Monique L.
Prickett, M. Dennis
Settlage, Robert E.
Kang, Lin
Michalak, Pawel
Vliet, Kent A.
Bishop, Barney M.
author_sort van Hoek, Monique L.
collection PubMed
description BACKGROUND: We report the sequencing, assembly and analysis of the genome of the Komodo dragon (Varanus komodoensis), the largest extant lizard, with a focus on antimicrobial host-defense peptides. The Komodo dragon diet includes carrion, and a complex milieu of bacteria, including potentially pathogenic strains, has been detected in the saliva of wild dragons. They appear to be unaffected, suggesting that dragons have robust defenses against infection. While little information is available regarding the molecular biology of reptile immunity, it is believed that innate immunity, which employs antimicrobial host-defense peptides including defensins and cathelicidins, plays a more prominent role in reptile immunity than it does in mammals. . RESULTS: High molecular weight genomic DNA was extracted from Komodo dragon blood cells. Subsequent sequencing and assembly of the genome from the collected DNA yielded a genome size of 1.6 Gb with 45x coverage, and the identification of 17,213 predicted genes. Through further analyses of the genome, we identified genes and gene-clusters corresponding to antimicrobial host-defense peptide genes. Multiple β-defensin-related gene clusters were identified, as well as a cluster of potential Komodo dragon ovodefensin genes located in close proximity to a cluster of Komodo dragon β-defensin genes. In addition to these defensins, multiple cathelicidin-like genes were also identified in the genome. Overall, 66 β-defensin genes, six ovodefensin genes and three cathelicidin genes were identified in the Komodo dragon genome. CONCLUSIONS: Genes with important roles in host-defense and innate immunity were identified in this newly sequenced Komodo dragon genome, suggesting that these organisms have a robust innate immune system. Specifically, multiple Komodo antimicrobial peptide genes were identified. Importantly, many of the antimicrobial peptide genes were found in gene clusters. We found that these innate immunity genes are conserved among reptiles, and the organization is similar to that seen in other avian and reptilian species. Having the genome of this important squamate will allow researchers to learn more about reptilian gene families and will be a valuable resource for researchers studying the evolution and biology of the endangered Komodo dragon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-6029-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-67169212019-09-04 The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters van Hoek, Monique L. Prickett, M. Dennis Settlage, Robert E. Kang, Lin Michalak, Pawel Vliet, Kent A. Bishop, Barney M. BMC Genomics Research Article BACKGROUND: We report the sequencing, assembly and analysis of the genome of the Komodo dragon (Varanus komodoensis), the largest extant lizard, with a focus on antimicrobial host-defense peptides. The Komodo dragon diet includes carrion, and a complex milieu of bacteria, including potentially pathogenic strains, has been detected in the saliva of wild dragons. They appear to be unaffected, suggesting that dragons have robust defenses against infection. While little information is available regarding the molecular biology of reptile immunity, it is believed that innate immunity, which employs antimicrobial host-defense peptides including defensins and cathelicidins, plays a more prominent role in reptile immunity than it does in mammals. . RESULTS: High molecular weight genomic DNA was extracted from Komodo dragon blood cells. Subsequent sequencing and assembly of the genome from the collected DNA yielded a genome size of 1.6 Gb with 45x coverage, and the identification of 17,213 predicted genes. Through further analyses of the genome, we identified genes and gene-clusters corresponding to antimicrobial host-defense peptide genes. Multiple β-defensin-related gene clusters were identified, as well as a cluster of potential Komodo dragon ovodefensin genes located in close proximity to a cluster of Komodo dragon β-defensin genes. In addition to these defensins, multiple cathelicidin-like genes were also identified in the genome. Overall, 66 β-defensin genes, six ovodefensin genes and three cathelicidin genes were identified in the Komodo dragon genome. CONCLUSIONS: Genes with important roles in host-defense and innate immunity were identified in this newly sequenced Komodo dragon genome, suggesting that these organisms have a robust innate immune system. Specifically, multiple Komodo antimicrobial peptide genes were identified. Importantly, many of the antimicrobial peptide genes were found in gene clusters. We found that these innate immunity genes are conserved among reptiles, and the organization is similar to that seen in other avian and reptilian species. Having the genome of this important squamate will allow researchers to learn more about reptilian gene families and will be a valuable resource for researchers studying the evolution and biology of the endangered Komodo dragon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-6029-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-30 /pmc/articles/PMC6716921/ /pubmed/31470795 http://dx.doi.org/10.1186/s12864-019-6029-y Text en © The Author(s). 2019 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 Hoek, Monique L.
Prickett, M. Dennis
Settlage, Robert E.
Kang, Lin
Michalak, Pawel
Vliet, Kent A.
Bishop, Barney M.
The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters
title The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters
title_full The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters
title_fullStr The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters
title_full_unstemmed The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters
title_short The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters
title_sort komodo dragon (varanus komodoensis) genome and identification of innate immunity genes and clusters
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716921/
https://www.ncbi.nlm.nih.gov/pubmed/31470795
http://dx.doi.org/10.1186/s12864-019-6029-y
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