Evidence map›Paper›PMID 40932566›Full record

ArticleMarine biotechnology (New York, N.Y.)2025

Comparative Transcriptomic Analysis Reveals Key Growth-Related Genes and Alternative Splicing Events in Siniperca scherzeri.

Hao Xu, Jian Jin, Yang Li, Yannian Wu, Zhiqiang Cheng, Maoyuan Wang, Xiaojun Ye, Mingyong Lai, Dongling Zhang

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Article in Marine biotechnology (New York, N.Y.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

9 authors.

Hao XuKey Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China.
Jian JinKey Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China.
Yang LiKey Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China.
Yannian WuKey Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China.
Zhiqiang ChengKey Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China.
Maoyuan WangFreshwater Fisheries Research Institute of Fujian Province, Fuzhou, China.
Xiaojun YeFreshwater Fisheries Research Institute of Fujian Province, Fuzhou, China.
Mingyong LaiFreshwater Fisheries Research Institute of Fujian Province, Fuzhou, China.
Dongling ZhangKey Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China. zhangdongling@jmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Siniperca scherzeri is an important aquaculture species in China with good disease resistance, but its growth rate is relatively slow. To uncover the molecular mechanisms underlying growth trait differences, this study employed RNA-seq technology to analyze the liver tissues of fast-growing (FG) and slow-growing (SG) individuals of S. scherzeri. A total of 875 differentially expressed genes (DEGs) and 622 differentially alternatively spliced genes (DSGs) were identified. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses revealed that the DEGs were mainly involved in skeletal development, extracellular matrix remodeling, signal transduction, and cell growth and apoptosis, whereas the DSGs were significantly enriched in processes such as RNA splicing and processing, protein degradation, ribosome biogenesis, muscle structure and contraction, and were associated with multiple energy metabolism and signaling pathways. Alternative splicing analysis revealed that, compared with the slow-growth group, the fast-growth group exhibited a higher abundance of alternative splicing events. These results suggest that the growth differences in S. scherzeri may stem from the coordinated regulation at both the transcriptional and splicing levels, thereby contributing to enhanced growth rates. These findings provide important insights into the molecular basis underlying growth differences in S. scherzeri and offer valuable resources for the identification of potential molecular markers and key functional genes for aquaculture breeding.

Indexed as

Alternative SplicingTranscriptomeAnimalsGene Expression ProfilingGene OntologyLiverAlternative splicingGrowthRNA-seqSiniperca scherzeri

Identifiers

PMID40932566

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