Feminization of channel catfish with 17β-oestradiol involves methylation and expression of a specific set of genes independent of the sex determination region

被引:6
作者
Wang, Wenwen [1 ]
Tan, Suxu [1 ]
Yang, Yujia [1 ]
Zhou, Tao [1 ,2 ]
Xing, De [1 ]
Su, Baofeng [1 ]
Wang, Jinhai [1 ]
Li, Shangjia [1 ]
Shang, Mei [1 ]
Gao, Dongya [3 ]
Dunham, Rex [1 ]
Liu, Zhanjiang [3 ]
机构
[1] Auburn Univ, Sch Fisheries Aquaculture & Aquat Sci, Auburn, AL 36849 USA
[2] Xiamen Univ, Coll Ocean & Earth Sci, Fujian Key Lab Genet & Breeding Marine Organisms, Xiamen, Fujian, Peoples R China
[3] Syracuse Univ, Dept Biol, Coll Arts & Sci, Syracuse, NY 13244 USA
基金
美国食品与农业研究所;
关键词
Sex reversal; methylation; oestrogen; transcription; sex differentiation; teleost; ZEBRAFISH DANIO-RERIO; DMRT1; EXPRESSION; DNA METHYLATION; SIGNAL-TRANSDUCTION; HORMONAL INDUCTION; GONADAL EXPRESSION; RAINBOW-TROUT; FOXL2; DIFFERENTIATION; AROMATASE;
D O I
10.1080/15592294.2022.2086725
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Exogenous oestrogen 17 beta-oestradiol (E2) has been shown to effectively induce feminization in teleosts. However, the molecular mechanisms underlying the process remain unclear. Here, we determined global DNA methylation and gene expression profiles of channel catfish (Ictalurus punctatus) during early sex differentiation after E2 treatment. Overall, the levels of global DNA methylation after E2 treatment were not significantly different from those of controls. However, a specific set of genes were differentially methylated, which included many sex differentiation-related pathways, such as MARK signalling, adrenergic signalling, Wnt signalling, GnRH signalling, ErbB signalling, and ECM-receptor interactions. Many genes involved in these pathways were also differentially expressed after E2 treatment. Specifically, E2 treatments resulted in upregulation of female-related genes and downregulation of male-related genes in genetic males during sex reversal. However, E2-induced sex reversal did not cause sex-specific changes in methylation profiles or gene expression within the sex determination region (SDR) on chromosome 4, suggesting that E2-induced sex reversal was a downstream process independent of the sex determination process that was regulated by sex-specific methylation within the SDR.
引用
收藏
页码:1820 / 1837
页数:18
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