Evidence map›Paper›PMID 41146024›Full record

ArticleBMC genomics2025

Genome-wide identification, expression analysis of taars (trace amine-associated receptors) and response to cadaverine and putrescine in Mandarin fish (Siniperca chuatsi).

Xiaoru Dong, Maolin Lv, Qiyao Luo, Xiao Jiang, Xu-Fang Liang

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Article in BMC genomics, 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xiaoru DongCollege of Fisheries, Chinese Perch Research Center, Huazhong Agricultural University, Wuhan , 430070, China.
Maolin LvHubei Hongshan Laboratory, College of Fisheries, Huazhong Agricultural University, Wuhan, 430070, China.
Qiyao LuoCollege of Fisheries, Chinese Perch Research Center, Huazhong Agricultural University, Wuhan , 430070, China.
Xiao JiangCollege of Fisheries, Chinese Perch Research Center, Huazhong Agricultural University, Wuhan , 430070, China.
Xu-Fang LiangCollege of Fisheries, Chinese Perch Research Center, Huazhong Agricultural University, Wuhan , 430070, China.

Funding

National Key Research and Development Program of China 2024YFD2401502
6 · The paper itself

Abstract

backgroundThe unique feeding behavior of Siniperca chuatsi (S. chuatsi), which exclusively consumes live fry and rejects dead fry, severely limits the development of its aquaculture industry. This rejection of dead fry likely stems from an aversion to necromones (death-associated odors). Although a subset of trace amine-associated receptors (TAARs) containing key conserved residues (Asp

resultsIn this study, we found that the aversion of S. chuatsi to dead prey is associated with necromones. Furthermore, we identified 68 taar family members in the S. chuatsi genome, distributed across six chromosomes, with 36 tandem duplication events generating 54 duplicated genes. Phylogenetic analysis classified taars into two classes, Class I and Class III, with a total of eight subfamilies. Synteny analysis revealed low synteny between the taars of S. chuatsi and Dicentrarchus labrax, with only 12 pairs of genes showing syntenic relationships. Protein sequence analysis demonstrated that taars contain amine recognition sites, N-glycosylation, and conserved cysteine structures, with high conservation and purifying selection observed within subfamilies. Subcellular localization revealed that TAARs are localized to the cell membrane and nucleus. Transcriptome data indicated that 61 taars are expressed in the olfactory epithelium, while only 19 are expressed in the brain. The response of representative taars to putrescine and cadaverine was divergent when comparing olfactory and brain tissues.

conclusionsThis study systematically identified the taar gene family in S. chuatsi, analyzing their evolutionary relationships, protein structures, subcellular localization, expression profiles in olfactory and brain tissues, and the response of selected TAARs to necromones (cadaverine and putrescine). This work establishes a foundation for further investigation into TAAR-mediated death odor recognition in S. chuatsi.

Indexed as

FishesFish ProteinsPerciformesPutrescineReceptors, G-Protein-CoupledAnimalsGene Expression ProfilingPhylogenySyntenyTrace Amine-Associated ReceptorsFish ProteinsPutrescineReceptors, G-Protein-CoupledTrace Amine-Associated ReceptorsExpression profilingNecromone detectionPurifying selectionSiniperca chuatsiSubcellular localizationTrace amine-associaed receptor (TAAR)

Identifiers

PMID41146024
PMCPMC12560584

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