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The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda
BACKGROUND: The genetics of development in the nematode Caenorhabditis elegans has been described in exquisite detail. The phylum Nematoda has two classes: Chromadorea (which includes C. elegans) and the Enoplea. While the development of many chromadorean species resembles closely that of C. elegans...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890508/ https://www.ncbi.nlm.nih.gov/pubmed/24373391 http://dx.doi.org/10.1186/1471-2164-14-923 |
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author | Schiffer, Philipp H Kroiher, Michael Kraus, Christopher Koutsovoulos, Georgios D Kumar, Sujai R Camps, Julia I Nsah, Ndifon A Stappert, Dominik Morris, Krystalynne Heger, Peter Altmüller, Janine Frommolt, Peter Nürnberg, Peter Thomas, W Kelley Blaxter, Mark L Schierenberg, Einhard |
author_facet | Schiffer, Philipp H Kroiher, Michael Kraus, Christopher Koutsovoulos, Georgios D Kumar, Sujai R Camps, Julia I Nsah, Ndifon A Stappert, Dominik Morris, Krystalynne Heger, Peter Altmüller, Janine Frommolt, Peter Nürnberg, Peter Thomas, W Kelley Blaxter, Mark L Schierenberg, Einhard |
author_sort | Schiffer, Philipp H |
collection | PubMed |
description | BACKGROUND: The genetics of development in the nematode Caenorhabditis elegans has been described in exquisite detail. The phylum Nematoda has two classes: Chromadorea (which includes C. elegans) and the Enoplea. While the development of many chromadorean species resembles closely that of C. elegans, enoplean nematodes show markedly different patterns of early cell division and cell fate assignment. Embryogenesis of the enoplean Romanomermis culicivorax has been studied in detail, but the genetic circuitry underpinning development in this species has not been explored. RESULTS: We generated a draft genome for R. culicivorax and compared its gene content with that of C. elegans, a second enoplean, the vertebrate parasite Trichinella spiralis, and a representative arthropod, Tribolium castaneum. This comparison revealed that R. culicivorax has retained components of the conserved ecdysozoan developmental gene toolkit lost in C. elegans. T. spiralis has independently lost even more of this toolkit than has C. elegans. However, the C. elegans toolkit is not simply depauperate, as many novel genes essential for embryogenesis in C. elegans are not found in, or have only extremely divergent homologues in R. culicivorax and T. spiralis. Our data imply fundamental differences in the genetic programmes not only for early cell specification but also others such as vulva formation and sex determination. CONCLUSIONS: Despite the apparent morphological conservatism, major differences in the molecular logic of development have evolved within the phylum Nematoda. R. culicivorax serves as a tractable system to contrast C. elegans and understand how divergent genomic and thus regulatory backgrounds nevertheless generate a conserved phenotype. The R. culicivorax draft genome will promote use of this species as a research model. |
format | Online Article Text |
id | pubmed-3890508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38905082014-01-15 The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda Schiffer, Philipp H Kroiher, Michael Kraus, Christopher Koutsovoulos, Georgios D Kumar, Sujai R Camps, Julia I Nsah, Ndifon A Stappert, Dominik Morris, Krystalynne Heger, Peter Altmüller, Janine Frommolt, Peter Nürnberg, Peter Thomas, W Kelley Blaxter, Mark L Schierenberg, Einhard BMC Genomics Research Article BACKGROUND: The genetics of development in the nematode Caenorhabditis elegans has been described in exquisite detail. The phylum Nematoda has two classes: Chromadorea (which includes C. elegans) and the Enoplea. While the development of many chromadorean species resembles closely that of C. elegans, enoplean nematodes show markedly different patterns of early cell division and cell fate assignment. Embryogenesis of the enoplean Romanomermis culicivorax has been studied in detail, but the genetic circuitry underpinning development in this species has not been explored. RESULTS: We generated a draft genome for R. culicivorax and compared its gene content with that of C. elegans, a second enoplean, the vertebrate parasite Trichinella spiralis, and a representative arthropod, Tribolium castaneum. This comparison revealed that R. culicivorax has retained components of the conserved ecdysozoan developmental gene toolkit lost in C. elegans. T. spiralis has independently lost even more of this toolkit than has C. elegans. However, the C. elegans toolkit is not simply depauperate, as many novel genes essential for embryogenesis in C. elegans are not found in, or have only extremely divergent homologues in R. culicivorax and T. spiralis. Our data imply fundamental differences in the genetic programmes not only for early cell specification but also others such as vulva formation and sex determination. CONCLUSIONS: Despite the apparent morphological conservatism, major differences in the molecular logic of development have evolved within the phylum Nematoda. R. culicivorax serves as a tractable system to contrast C. elegans and understand how divergent genomic and thus regulatory backgrounds nevertheless generate a conserved phenotype. The R. culicivorax draft genome will promote use of this species as a research model. BioMed Central 2013-12-27 /pmc/articles/PMC3890508/ /pubmed/24373391 http://dx.doi.org/10.1186/1471-2164-14-923 Text en Copyright © 2013 Schiffer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Schiffer, Philipp H Kroiher, Michael Kraus, Christopher Koutsovoulos, Georgios D Kumar, Sujai R Camps, Julia I Nsah, Ndifon A Stappert, Dominik Morris, Krystalynne Heger, Peter Altmüller, Janine Frommolt, Peter Nürnberg, Peter Thomas, W Kelley Blaxter, Mark L Schierenberg, Einhard The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda |
title | The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda |
title_full | The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda |
title_fullStr | The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda |
title_full_unstemmed | The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda |
title_short | The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda |
title_sort | genome of romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in nematoda |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890508/ https://www.ncbi.nlm.nih.gov/pubmed/24373391 http://dx.doi.org/10.1186/1471-2164-14-923 |
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