LncRNA-Mediated Tissue-Specific Plastic Responses to Salinity Changes in Oysters

Salinity is a key environmental factor influencing the survival of aquatic organisms, and transcriptional plasticity is a crucial emergency response to environmental changes. However, most transcriptomic studies on salinity responses have not explored the expression patterns and regulatory mechanisms across different tissues. The Suminoe oyster (<i>Crassostrea ariakensis</i>), a sessile estuarine species that inhabits fluctuating salinity environments, provides an excellent model for studying the molecular basis of salinity response divergence. All eight tissues responded to acute salinity stresses and exhibited distinct tissue-specific expression patterns in both mRNA and long non-coding RNA (lncRNA) profiles across three salinity conditions. The hepatopancreas and striated muscle were identified as tissues specifically sensitive to hyper- and hypo-saline stress, respectively, based on the number, expression pattern, and plasticity of differentially expressed genes (DEGs). We established lncRNA-mRNA regulatory relationships that environmentally responsive lncRNAs enhanced DEGs' expression and underpinning tissue-specific responses. Under moderate stress, the hepatopancreas and striated muscle initiated positive responses related to water transport and shell closure, respectively. Under severe stress, the hepatopancreas activated cellular resistance pathways, while the striated muscle experienced significant cell death. Our findings provide insights into lncRNA-mediated, tissue-specific environmental responses and lay the foundation for further research into the adaptive evolution of tissue-specific regulation.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-05-09
DOI
https://doi.org/10.3390/ijms26104523
Citations
3
Primary Topic
Physiological and biochemical adaptations
Type
article
Field-Weighted Citation Impact
5.15

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article

LncRNA-Mediated Tissue-Specific Plastic Responses to Salinity Changes in Oysters

Mengshi Zhang, M.‐R. Huo, Guofan Zhang, Minjie Zhao et al.
3 citations
International Journal of Molecular Sciences
Physiological and biochemical adaptations
5.15
article

LncRNA-Mediated Tissue-Specific Plastic Responses to Salinity Changes in Oysters

Mengshi Zhang, M.‐R. Huo, Guofan Zhang, Minjie Zhao, Ao Li, Li Li, Wei Wang, Luping Wang, Jinlong Zhao, Jingying Deng
article en
3 citations

Abstract

Salinity is a key environmental factor influencing the survival of aquatic organisms, and transcriptional plasticity is a crucial emergency response to environmental changes. However, most transcriptomic studies on salinity responses have not explored the expression patterns and regulatory mechanisms across different tissues. The Suminoe oyster (<i>Crassostrea ariakensis</i>), a sessile estuarine species that inhabits fluctuating salinity environments, provides an excellent model for studying the molecular basis of salinity response divergence. All eight tissues responded to acute salinity stresses and exhibited distinct tissue-specific expression patterns in both mRNA and long non-coding RNA (lncRNA) profiles across three salinity conditions. The hepatopancreas and striated muscle were identified as tissues specifically sensitive to hyper- and hypo-saline stress, respectively, based on the number, expression pattern, and plasticity of differentially expressed genes (DEGs). We established lncRNA-mRNA regulatory relationships that environmentally responsive lncRNAs enhanced DEGs' expression and underpinning tissue-specific responses. Under moderate stress, the hepatopancreas and striated muscle initiated positive responses related to water transport and shell closure, respectively. Under severe stress, the hepatopancreas activated cellular resistance pathways, while the striated muscle experienced significant cell death. Our findings provide insights into lncRNA-mediated, tissue-specific environmental responses and lay the foundation for further research into the adaptive evolution of tissue-specific regulation.

International Journal of Molecular SciencesVol. 26(10)
Qingdao Agricultural University (CN), Chinese Academy of Sciences (CN), Institute of Oceanology (CN), Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (CN), Qingdao National Laboratory for Marine Science and Technology (CN), Zhanjiang Experimental Station (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Youth Innovation Promotion Association of the Chinese Academy of Sciences, Shanghai Ocean University, National Key Research and Development Program of China, Guangxi Key Research and Development Program
Life below water
Openalex Percentile: Top 6%
Physiological and biochemical adaptations
5.15
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