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Transcriptome analysis elucidates key developmental components of bryozoan lophophore development

The most recent phylogenomic study suggested that Bryozoa (Ectoprocta), Brachiopoda, and Phoronida are monophyletic, implying that the lophophore of bryozoans, phoronids and brachiopods is a synapomorphy. Understanding the molecular mechanisms of the lophophore development of the Lophophorata clade...

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Autores principales: Wong, Yue Him, Ryu, Taewoo, Seridi, Loqmane, Ghosheh, Yanal, Bougouffa, Salim, Qian, Pei-Yuan, Ravasi, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192642/
https://www.ncbi.nlm.nih.gov/pubmed/25300304
http://dx.doi.org/10.1038/srep06534
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author Wong, Yue Him
Ryu, Taewoo
Seridi, Loqmane
Ghosheh, Yanal
Bougouffa, Salim
Qian, Pei-Yuan
Ravasi, Timothy
author_facet Wong, Yue Him
Ryu, Taewoo
Seridi, Loqmane
Ghosheh, Yanal
Bougouffa, Salim
Qian, Pei-Yuan
Ravasi, Timothy
author_sort Wong, Yue Him
collection PubMed
description The most recent phylogenomic study suggested that Bryozoa (Ectoprocta), Brachiopoda, and Phoronida are monophyletic, implying that the lophophore of bryozoans, phoronids and brachiopods is a synapomorphy. Understanding the molecular mechanisms of the lophophore development of the Lophophorata clade can therefore provide us a new insight into the formation of the diverse morphological traits in metazoans. In the present study, we profiled the transcriptome of the Bryozoan (Ectoproct) Bugula neritina during the swimming larval stage (SW) and the early (4 h) and late (24 h) metamorphic stages using the Illumina HiSeq2000 platform. Various genes that function in development, the immune response and neurogenesis showed differential expression levels during metamorphosis. In situ hybridization of 23 genes that participate in the Wnt, BMP, Notch, and Hedgehog signaling pathways revealed their regulatory roles in the development of the lophophore and the ancestrula digestive tract. Our findings support the hypothesis that developmental precursors of the lophophore and the ancestrula digestive tract are pre-patterned by the differential expression of key developmental genes according to their fate. This study provides a foundation to better understand the developmental divergence and/or convergence among developmental precursors of the lophophore of bryozoans, branchiopods and phoronids.
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spelling pubmed-41926422014-10-21 Transcriptome analysis elucidates key developmental components of bryozoan lophophore development Wong, Yue Him Ryu, Taewoo Seridi, Loqmane Ghosheh, Yanal Bougouffa, Salim Qian, Pei-Yuan Ravasi, Timothy Sci Rep Article The most recent phylogenomic study suggested that Bryozoa (Ectoprocta), Brachiopoda, and Phoronida are monophyletic, implying that the lophophore of bryozoans, phoronids and brachiopods is a synapomorphy. Understanding the molecular mechanisms of the lophophore development of the Lophophorata clade can therefore provide us a new insight into the formation of the diverse morphological traits in metazoans. In the present study, we profiled the transcriptome of the Bryozoan (Ectoproct) Bugula neritina during the swimming larval stage (SW) and the early (4 h) and late (24 h) metamorphic stages using the Illumina HiSeq2000 platform. Various genes that function in development, the immune response and neurogenesis showed differential expression levels during metamorphosis. In situ hybridization of 23 genes that participate in the Wnt, BMP, Notch, and Hedgehog signaling pathways revealed their regulatory roles in the development of the lophophore and the ancestrula digestive tract. Our findings support the hypothesis that developmental precursors of the lophophore and the ancestrula digestive tract are pre-patterned by the differential expression of key developmental genes according to their fate. This study provides a foundation to better understand the developmental divergence and/or convergence among developmental precursors of the lophophore of bryozoans, branchiopods and phoronids. Nature Publishing Group 2014-10-10 /pmc/articles/PMC4192642/ /pubmed/25300304 http://dx.doi.org/10.1038/srep06534 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Article
Wong, Yue Him
Ryu, Taewoo
Seridi, Loqmane
Ghosheh, Yanal
Bougouffa, Salim
Qian, Pei-Yuan
Ravasi, Timothy
Transcriptome analysis elucidates key developmental components of bryozoan lophophore development
title Transcriptome analysis elucidates key developmental components of bryozoan lophophore development
title_full Transcriptome analysis elucidates key developmental components of bryozoan lophophore development
title_fullStr Transcriptome analysis elucidates key developmental components of bryozoan lophophore development
title_full_unstemmed Transcriptome analysis elucidates key developmental components of bryozoan lophophore development
title_short Transcriptome analysis elucidates key developmental components of bryozoan lophophore development
title_sort transcriptome analysis elucidates key developmental components of bryozoan lophophore development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192642/
https://www.ncbi.nlm.nih.gov/pubmed/25300304
http://dx.doi.org/10.1038/srep06534
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