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Comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa
Lophotrochozoan species exhibit wide morphological diversity; however, the molecular basis underlying this diversity remains unclear. Here, we explored the evolution of Notch pathway genes across 37 metazoan species via phylogenetic and molecular evolutionary studies with emphasis on the lophotrocho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166818/ https://www.ncbi.nlm.nih.gov/pubmed/34059772 http://dx.doi.org/10.1038/s41598-021-90800-8 |
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author | He, Xin Wu, Fucun Zhang, Linlin Li, Li Zhang, Guofan |
author_facet | He, Xin Wu, Fucun Zhang, Linlin Li, Li Zhang, Guofan |
author_sort | He, Xin |
collection | PubMed |
description | Lophotrochozoan species exhibit wide morphological diversity; however, the molecular basis underlying this diversity remains unclear. Here, we explored the evolution of Notch pathway genes across 37 metazoan species via phylogenetic and molecular evolutionary studies with emphasis on the lophotrochozoans. We displayed the components of Notch pathway in metazoans and found that Delta and Hes/Hey-related genes, as well as their functional domains, are duplicated in lophotrochozoans. Comparative transcriptomics analyses allow us to pinpoint sequence divergence of multigene families in the Notch signalling pathway. We identified the duplication mechanism of a mollusc-specific gene, Delta2, and found it displayed complementary expression throughout development. Furthermore, we found the functional diversification not only in expanded genes in the Notch pathway (Delta and Hes/Hey-related genes), but also in evolutionary conservative genes (Notch, Presenilin, and Su(H)). Together, this comprehensive study demonstrates conservation and divergence within the Notch pathway, reveals evolutionary relationships among metazoans, and provides evidence for the occurrence of developmental diversity in lophotrochozoans, as well as a basis for future gene function studies. |
format | Online Article Text |
id | pubmed-8166818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81668182021-06-01 Comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa He, Xin Wu, Fucun Zhang, Linlin Li, Li Zhang, Guofan Sci Rep Article Lophotrochozoan species exhibit wide morphological diversity; however, the molecular basis underlying this diversity remains unclear. Here, we explored the evolution of Notch pathway genes across 37 metazoan species via phylogenetic and molecular evolutionary studies with emphasis on the lophotrochozoans. We displayed the components of Notch pathway in metazoans and found that Delta and Hes/Hey-related genes, as well as their functional domains, are duplicated in lophotrochozoans. Comparative transcriptomics analyses allow us to pinpoint sequence divergence of multigene families in the Notch signalling pathway. We identified the duplication mechanism of a mollusc-specific gene, Delta2, and found it displayed complementary expression throughout development. Furthermore, we found the functional diversification not only in expanded genes in the Notch pathway (Delta and Hes/Hey-related genes), but also in evolutionary conservative genes (Notch, Presenilin, and Su(H)). Together, this comprehensive study demonstrates conservation and divergence within the Notch pathway, reveals evolutionary relationships among metazoans, and provides evidence for the occurrence of developmental diversity in lophotrochozoans, as well as a basis for future gene function studies. Nature Publishing Group UK 2021-05-31 /pmc/articles/PMC8166818/ /pubmed/34059772 http://dx.doi.org/10.1038/s41598-021-90800-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article He, Xin Wu, Fucun Zhang, Linlin Li, Li Zhang, Guofan Comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa |
title | Comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa |
title_full | Comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa |
title_fullStr | Comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa |
title_full_unstemmed | Comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa |
title_short | Comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa |
title_sort | comparative and evolutionary analyses reveal conservation and divergence of the notch pathway in lophotrochozoa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166818/ https://www.ncbi.nlm.nih.gov/pubmed/34059772 http://dx.doi.org/10.1038/s41598-021-90800-8 |
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