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Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks

BACKGROUND: Parasitism is a major ecological niche for a variety of nematodes. Multiple nematode lineages have specialized as pathogens, including deadly parasites of insects that are used in biological control. We have sequenced and analyzed the draft genomes and transcriptomes of the entomopathoge...

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Autores principales: Dillman, Adler R., Macchietto, Marissa, Porter, Camille F., Rogers, Alicia, Williams, Brian, Antoshechkin, Igor, Lee, Ming-Min, Goodwin, Zane, Lu, Xiaojun, Lewis, Edwin E., Goodrich-Blair, Heidi, Stock, S. Patricia, Adams, Byron J., Sternberg, Paul W., Mortazavi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578762/
https://www.ncbi.nlm.nih.gov/pubmed/26392177
http://dx.doi.org/10.1186/s13059-015-0746-6
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author Dillman, Adler R.
Macchietto, Marissa
Porter, Camille F.
Rogers, Alicia
Williams, Brian
Antoshechkin, Igor
Lee, Ming-Min
Goodwin, Zane
Lu, Xiaojun
Lewis, Edwin E.
Goodrich-Blair, Heidi
Stock, S. Patricia
Adams, Byron J.
Sternberg, Paul W.
Mortazavi, Ali
author_facet Dillman, Adler R.
Macchietto, Marissa
Porter, Camille F.
Rogers, Alicia
Williams, Brian
Antoshechkin, Igor
Lee, Ming-Min
Goodwin, Zane
Lu, Xiaojun
Lewis, Edwin E.
Goodrich-Blair, Heidi
Stock, S. Patricia
Adams, Byron J.
Sternberg, Paul W.
Mortazavi, Ali
author_sort Dillman, Adler R.
collection PubMed
description BACKGROUND: Parasitism is a major ecological niche for a variety of nematodes. Multiple nematode lineages have specialized as pathogens, including deadly parasites of insects that are used in biological control. We have sequenced and analyzed the draft genomes and transcriptomes of the entomopathogenic nematode Steinernema carpocapsae and four congeners (S. scapterisci, S. monticolum, S. feltiae, and S. glaseri). RESULTS: We used these genomes to establish phylogenetic relationships, explore gene conservation across species, and identify genes uniquely expanded in insect parasites. Protein domain analysis in Steinernema revealed a striking expansion of numerous putative parasitism genes, including certain protease and protease inhibitor families, as well as fatty acid- and retinol-binding proteins. Stage-specific gene expression of some of these expanded families further supports the notion that they are involved in insect parasitism by Steinernema. We show that sets of novel conserved non-coding regulatory motifs are associated with orthologous genes in Steinernema and Caenorhabditis. CONCLUSIONS: We have identified a set of expanded gene families that are likely to be involved in parasitism. We have also identified a set of non-coding motifs associated with groups of orthologous genes in Steinernema and Caenorhabditis involved in neurogenesis and embryonic development that are likely part of conserved protein–DNA relationships shared between these two genera. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0746-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-45787622015-09-23 Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks Dillman, Adler R. Macchietto, Marissa Porter, Camille F. Rogers, Alicia Williams, Brian Antoshechkin, Igor Lee, Ming-Min Goodwin, Zane Lu, Xiaojun Lewis, Edwin E. Goodrich-Blair, Heidi Stock, S. Patricia Adams, Byron J. Sternberg, Paul W. Mortazavi, Ali Genome Biol Research BACKGROUND: Parasitism is a major ecological niche for a variety of nematodes. Multiple nematode lineages have specialized as pathogens, including deadly parasites of insects that are used in biological control. We have sequenced and analyzed the draft genomes and transcriptomes of the entomopathogenic nematode Steinernema carpocapsae and four congeners (S. scapterisci, S. monticolum, S. feltiae, and S. glaseri). RESULTS: We used these genomes to establish phylogenetic relationships, explore gene conservation across species, and identify genes uniquely expanded in insect parasites. Protein domain analysis in Steinernema revealed a striking expansion of numerous putative parasitism genes, including certain protease and protease inhibitor families, as well as fatty acid- and retinol-binding proteins. Stage-specific gene expression of some of these expanded families further supports the notion that they are involved in insect parasitism by Steinernema. We show that sets of novel conserved non-coding regulatory motifs are associated with orthologous genes in Steinernema and Caenorhabditis. CONCLUSIONS: We have identified a set of expanded gene families that are likely to be involved in parasitism. We have also identified a set of non-coding motifs associated with groups of orthologous genes in Steinernema and Caenorhabditis involved in neurogenesis and embryonic development that are likely part of conserved protein–DNA relationships shared between these two genera. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0746-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-21 2015 /pmc/articles/PMC4578762/ /pubmed/26392177 http://dx.doi.org/10.1186/s13059-015-0746-6 Text en © Dillman et al. 2015 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
Dillman, Adler R.
Macchietto, Marissa
Porter, Camille F.
Rogers, Alicia
Williams, Brian
Antoshechkin, Igor
Lee, Ming-Min
Goodwin, Zane
Lu, Xiaojun
Lewis, Edwin E.
Goodrich-Blair, Heidi
Stock, S. Patricia
Adams, Byron J.
Sternberg, Paul W.
Mortazavi, Ali
Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks
title Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks
title_full Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks
title_fullStr Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks
title_full_unstemmed Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks
title_short Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks
title_sort comparative genomics of steinernema reveals deeply conserved gene regulatory networks
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578762/
https://www.ncbi.nlm.nih.gov/pubmed/26392177
http://dx.doi.org/10.1186/s13059-015-0746-6
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