4.8 Article

2,4-Dichlorophenol Increases Primordial Germ Cell Numbers via ESR2a-Dependent Pathway in Zebrafish Larvae

期刊

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c05212

关键词

2; 4-DCP; Sex differentiation; Estrogen receptor signaling; Molecular docking; Estrogenic effects

资金

  1. Second Tibetan Plateau Scientific Expedition and Research Program (STEP) [2021QZKK0204]
  2. National Natural Science Foundation of China [31670517]
  3. Natural Science Foundation of Gansu Province, China [1606RJZA080]
  4. Fundamental Research Funds for the Central Universities [lzujbky-2019-73]
  5. Double First-Class Research Start-up Funds of Lanzhou University [561119206]

向作者/读者索取更多资源

This study investigates the effects of 2,4-dichlorophenol (2,4-DCP) on the number of primordial germ cells (PGCs) in zebrafish. The results show that 2,4-DCP exposure increases PGC numbers and upregulates the expression of PGC marker genes. It is also found that 2,4-DCP interacts with estrogen receptor 2a (ESR2a) and the ESR2a signaling pathway plays a role in mediating the increase in PGC numbers.
Previous studies have reported the feminizing effects of 2,4-dichlorophenol (2,4-DCP) on zebrafish (Danio rerio). However, the effect of 2,4-DCP on the number of primordial germ cells (PGCs), an indicator for early sex differentiation, remains elusive. In the present study, Tg (piwil1:egfp-UTR nanos3) zebrafish (GFP-labeled PGCs) were treated with 2,4-DCP (10, 20, and 40 mu g/ L) from 5 to 15 days postfertilization to explore the effect on PGC numbers and to elucidate associated molecular mechanisms. The results showed that 2,4-DCP exposure increased PGC numbers, as evidenced by larger GFP fluorescent areas, upregulated expressions of PGC marker genes (vasa and dnd), and raised the female ratio. Notably, the mRNA level of estrogen receptor 2a (esr2a) was also increased subsequently. Moreover, docking studies revealed stable 2,4-DCP interactions with ESR2a, speculating a role of ESR2a signaling pathway in 2,4-DCP toxicity. Furthermore, in esr2a knockout (esr2a-/-) zebrafish, the effects of 2,4-DCP were considerably minimized, proving the involvement of the ESR2a signaling pathway in the 2,4-DCP-mediated increase in PGC numbers. Dual-luciferase reporter gene assay and point mutation studies demonstrated that 2,4-DCP-stimulated promoter activity was mediated by estrogen response element (ERE) located in -686/-674 of the vasa promoter and -731/-719 of the dnd promoter. Overall, 2,4-DCP can potentially enhance the expression of vasa and dnd by binding to zebrafish ESR2a, thus leading to increased PGC numbers and subsequent female-biased sex differentiation.

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