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Hexafluoropropylene oxide trimer acid (HFPO-TA) disrupts sex differentiation of zebrafish (Danio rerio) via an epigenetic mechanism of DNA methylation.
Yang, Dan; Li, Fanghua; Zhao, Xiaohui; Dong, Shasha; Song, Guobin; Wang, Haonan; Li, Xiaoying; Ding, Guanghui.
Afiliación
  • Yang D; College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, China.
  • Li F; College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, China.
  • Zhao X; College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, China.
  • Dong S; College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, China.
  • Song G; College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, China.
  • Wang H; College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, China.
  • Li X; College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, China.
  • Ding G; College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, China. Electronic address: guanghuiding@dlmu.edu.cn.
Aquat Toxicol ; 275: 107077, 2024 Oct.
Article en En | MEDLINE | ID: mdl-39236549
ABSTRACT
Hexafluoropropylene oxide trimer acid (HFPO-TA), an alternative to perfluorooctanoic acid, has been shown to have estrogenic effects. However, its potential to disrupt fish sex differentiation during gonadal development remains unknown. Therefore, this study exposed zebrafish to HFPO-TA from approximately 2 hours post fertilization (hpf) to 60 days post fertilization (dpf) to investigate its effects on sex differentiation. Results indicated that HFPO-TA disrupted steroid hormone homeostasis, delayed gonadal development in both sexes, and resulted in a female-skewed sex ratio in zebrafish. HFPO-TA exposure up-regulated gene expressions of cyp19a1a, esr1, vtg1 and foxl2, while down-regulated those of amh, sox9a and dmrt1. These suggested that HFPO-TA dysregulated the expressions of key genes related to sex differentiation of zebrafish, promoted the production and activation of estrogen, and further induced the feminization. Interestingly, we observed promoter hypomethylation of cyp19a1a and promoter hypermethylation of amh in male zebrafish, which were negatively associated with their gene expressions. These suggested that HFPO-TA dysregulated these key genes through DNA methylation in their promoters. Therefore, the HFPO-TA disrupted the sex differentiation of zebrafish through an epigenetic mechanism involving DNA methylation, ultimately skewing the sex ratio towards females. Overall, this study demonstrated adverse effects of HFPO-TA on fish sex differentiation and provided novel insights into the underlying epigenetic mechanism.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Diferenciación Sexual / Contaminantes Químicos del Agua / Pez Cebra / Metilación de ADN / Epigénesis Genética Límite: Animals Idioma: En Revista: Aquat Toxicol Asunto de la revista: BIOLOGIA / TOXICOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Diferenciación Sexual / Contaminantes Químicos del Agua / Pez Cebra / Metilación de ADN / Epigénesis Genética Límite: Animals Idioma: En Revista: Aquat Toxicol Asunto de la revista: BIOLOGIA / TOXICOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China