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Endocrine Disruption in Freshwater Cladocerans: Transcriptomic Network Perspectives on TBOEP and PFECHS Impacts in Daphnia magnaopen access

Authors
Kim, Hyun WooYun, Seok-GyuPark, Ju YeonLee, JunHan, Jun PyoShin, Dong YeopLee, Jong HunCho, Eun-MinSeo, Young Rok
Issue Date
Dec-2025
Publisher
MDPI
Keywords
<italic>Daphnia magna</italic>; endocrine disruption; TBOEP; PFECHS; transcriptomic analysis; adverse outcome pathway (AOP)
Citation
International Journal of Molecular Sciences, v.26, no.24, pp 1 - 17
Pages
17
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Molecular Sciences
Volume
26
Number
24
Start Page
1
End Page
17
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/62714
DOI
10.3390/ijms262412146
ISSN
1661-6596
1422-0067
Abstract
Freshwater cladocerans such as Daphnia magna (D. magna) are keystone grazers whose hormone-regulated life history traits make them sensitive sentinels of endocrine-disrupting chemicals (EDCs). The organophosphate flame-retardant tris(2-butoxyethyl) phosphate (TBOEP) and perfluoroethylcyclohexane sulfonate (PFECHS) now co-occur at ng L-1-mu g L-1 in surface waters, yet their chronic sub-lethal impacts on invertebrate endocrine networks remain unclear. We analysed two publicly available 21-day microarray datasets (TBOEP: GSE55132; PFECHS: GSE75607) using gene ontology enrichment, STRING protein interaction networks, Drosophila phenotype mapping, and KEGG (Kyoto Encyclopaedia of Genes and Genomes)-anchored frameworks to build putative adverse outcome pathways (AOPs) for D. magna. Differentially expressed genes were clustered into functional modules and hub nodes were ranked by degree and betweenness. TBOEP suppressed moulting and growth, altering 1157 genes enriched for metabolism and membrane processes; hubs VRK1, MIB2, and adenylosuccinate synthetase formed a muscle anatomical development sub-network. PFECHS down-regulated vitellogenin and shifted 879 genes dominated by oxidative-stress and glutathione-metabolism signatures; central nodes UBC9, eIF4A-III, Tra-2 alpha, and HDAC1 linked meiotic-cycle, oogenesis, and cyclic-compound binding. Despite chemical dissimilarity, both compounds converged on Wnt-signalling nodes-TBOEP via presenilin-1, and PFECHS via CK1 epsilon/CK2-thereby reducing TCF/LEF-dependent transcription. Predicted outcomes include impaired oocyte maturation, reduced fecundity, and stunted body size, consistent with observed decreases in length and vitellogenin protein. Our network analysis, based on high-dose, sub-lethal exposures used in the underlying microarray studies, indicates that TBOEP- and PFECHS-induced perturbations can destabilise endocrine, developmental, and metabolic pathways in D. magna without overt lethality, and highlights Wnt-centred key events and hub genes as candidate biomarkers to be evaluated in future low-dose studies that use environmentally realistic exposure scenarios. Hub genes and Wnt-mediated key events emerge as sensitive biomarkers for monitoring mixed EDC exposure.
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