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Integrated mRNA and miRNA transcriptomic analysis reveals the response of Rapana venosa to the metamorphic inducer (juvenile oysters)

Metamorphosis, as a critical developmental event, controls the population dynamics of most marine invertebrates, especially some carnivorous gastropods that feed on bivalves, whose population dynamics not only affect the maintenance of the ecological balance but also impact the protection of bivalve...

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Autores principales: Yang, Mei-Jie, Song, Hao, Shi, Pu, Liang, Jian, Hu, Zhi, Zhou, Cong, Hu, Peng-Peng, Yu, Zheng-Lin, Zhang, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826900/
https://www.ncbi.nlm.nih.gov/pubmed/36659925
http://dx.doi.org/10.1016/j.csbj.2022.12.047
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author Yang, Mei-Jie
Song, Hao
Shi, Pu
Liang, Jian
Hu, Zhi
Zhou, Cong
Hu, Peng-Peng
Yu, Zheng-Lin
Zhang, Tao
author_facet Yang, Mei-Jie
Song, Hao
Shi, Pu
Liang, Jian
Hu, Zhi
Zhou, Cong
Hu, Peng-Peng
Yu, Zheng-Lin
Zhang, Tao
author_sort Yang, Mei-Jie
collection PubMed
description Metamorphosis, as a critical developmental event, controls the population dynamics of most marine invertebrates, especially some carnivorous gastropods that feed on bivalves, whose population dynamics not only affect the maintenance of the ecological balance but also impact the protection of bivalve resources; therefore, the metamorphosis of carnivorous gastropods deserve attention. Here, we investigated the mechanism underlying the response of the carnivorous gastropod Rapana venosa to its metamorphic inducer juvenile oysters through integrated analysis of miRNA and mRNA profiles. According to the results, we speculated that the AMPK signaling pathway may be the critical regulator in the response to juvenile oysters in R. venosa competent larvae. The NF-kB and JAK-STAT signaling pathways that regulated apoptosis were also activated by the metamorphic inducer, which may result in the degeneration of the velum. Additionally, the significant changes in the expression of the SARP-19 precursor gene and protein cibby homolog 1-like gene may indicate that these signaling pathways also regulate growth and development during metamorphosis. This study provides further evidence that juvenile oysters can induce metamorphosis of R. venosa at the transcriptional level, which expands our understanding of the metamorphosis mechanism in carnivorous gastropods.
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spelling pubmed-98269002023-01-18 Integrated mRNA and miRNA transcriptomic analysis reveals the response of Rapana venosa to the metamorphic inducer (juvenile oysters) Yang, Mei-Jie Song, Hao Shi, Pu Liang, Jian Hu, Zhi Zhou, Cong Hu, Peng-Peng Yu, Zheng-Lin Zhang, Tao Comput Struct Biotechnol J Research Article Metamorphosis, as a critical developmental event, controls the population dynamics of most marine invertebrates, especially some carnivorous gastropods that feed on bivalves, whose population dynamics not only affect the maintenance of the ecological balance but also impact the protection of bivalve resources; therefore, the metamorphosis of carnivorous gastropods deserve attention. Here, we investigated the mechanism underlying the response of the carnivorous gastropod Rapana venosa to its metamorphic inducer juvenile oysters through integrated analysis of miRNA and mRNA profiles. According to the results, we speculated that the AMPK signaling pathway may be the critical regulator in the response to juvenile oysters in R. venosa competent larvae. The NF-kB and JAK-STAT signaling pathways that regulated apoptosis were also activated by the metamorphic inducer, which may result in the degeneration of the velum. Additionally, the significant changes in the expression of the SARP-19 precursor gene and protein cibby homolog 1-like gene may indicate that these signaling pathways also regulate growth and development during metamorphosis. This study provides further evidence that juvenile oysters can induce metamorphosis of R. venosa at the transcriptional level, which expands our understanding of the metamorphosis mechanism in carnivorous gastropods. Research Network of Computational and Structural Biotechnology 2022-12-30 /pmc/articles/PMC9826900/ /pubmed/36659925 http://dx.doi.org/10.1016/j.csbj.2022.12.047 Text en © 2023 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Yang, Mei-Jie
Song, Hao
Shi, Pu
Liang, Jian
Hu, Zhi
Zhou, Cong
Hu, Peng-Peng
Yu, Zheng-Lin
Zhang, Tao
Integrated mRNA and miRNA transcriptomic analysis reveals the response of Rapana venosa to the metamorphic inducer (juvenile oysters)
title Integrated mRNA and miRNA transcriptomic analysis reveals the response of Rapana venosa to the metamorphic inducer (juvenile oysters)
title_full Integrated mRNA and miRNA transcriptomic analysis reveals the response of Rapana venosa to the metamorphic inducer (juvenile oysters)
title_fullStr Integrated mRNA and miRNA transcriptomic analysis reveals the response of Rapana venosa to the metamorphic inducer (juvenile oysters)
title_full_unstemmed Integrated mRNA and miRNA transcriptomic analysis reveals the response of Rapana venosa to the metamorphic inducer (juvenile oysters)
title_short Integrated mRNA and miRNA transcriptomic analysis reveals the response of Rapana venosa to the metamorphic inducer (juvenile oysters)
title_sort integrated mrna and mirna transcriptomic analysis reveals the response of rapana venosa to the metamorphic inducer (juvenile oysters)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826900/
https://www.ncbi.nlm.nih.gov/pubmed/36659925
http://dx.doi.org/10.1016/j.csbj.2022.12.047
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