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Transcriptional regulation of IAG by dsx and foxl-2 in mud crab (Scylla paramamosain)
被引:5
|作者:
Liao, Jiaqian
[1
,2
]
Wan, Haifu
[1
,2
]
Zhang, Ziping
[3
]
Sheng, Yinshen
[1
,2
]
Jia, Xiwei
[1
,2
]
Wang, Yilei
[1
,2
]
机构:
[1] Jimei Univ, Fisheries Coll, Key Lab Hlth Mariculture East China Sea, Minist Agr & Rural Affairs, Xiamen 361021, Peoples R China
[2] Fujian Engn Res Ctr Aquat Breeding & Hlth Aquacult, Xiamen 361021, Peoples R China
[3] Fujian Agr & Forestry Univ, Coll Marine Sci, Fuzhou 350002, Peoples R China
关键词:
IAG;
Dsx;
Foxl-2;
Transcriptional regulation;
Scylla paramamosain;
ANDROGENIC GLAND HORMONE;
INSULIN-LIKE GENE;
MOLECULAR-IDENTIFICATION;
DOUBLESEX GENE;
EXPRESSION;
DIFFERENTIATION;
VARIANTS;
GENDER;
SHRIMP;
D O I:
10.1016/j.ygcen.2023.114396
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Scylla paramamosain is an important cultured crab species on the southeast coast of China. However, the mo-lecular regulation mechanism of its gonadal development still has not been thoroughly studied. Dsx (doublesex) and foxl-2 (forkhead transcription factor gene 2) are important transcription factors involved in gonadal development. So far, studies on the functions of dsx and foxl-2 in crustaceans are very limited. Insulin-like androgenic gland hormone (IAG) is an effector molecule that regulates the differentiation, development and sex maintenance of testes in crustaceans. In this study, the promoter region of Sp-IAG was predicted, and several potential binding sites of dsx and foxl-2 were found. Site-directed mutagenesis was performed on the predicted potential binding sites, and their promoter activity was analyzed. The results showed that there was a dsx and a foxl-2 binding site, respectively, that could regulate the expression of Sp-IAG. In order to verify the regulatory effect of these two transcription factors on Sp-IAG, we constructed the expression plasmids of dsx and foxl-2 and co-transfected them into HEK293T cell lines with the promoter of Sp-IAG, respectively. The results showed that dsx could significantly promote the expression of Sp-IAG, while foxl-2 could inhibit its expression substantially. Then we carried out in vivo RNA interference experiment on mud crabs. The expression of dsx and foxl-2 in crabs was interfered respectively. The results of qRT-PCR showed that the expression of Sp-IAG was significantly inhibited after interfering with dsx, while significantly increased after interfering with foxl-2, which was consistent with the cell experiment. In conclusion, dsx and foxl-2 transcription factors play opposite roles in regulating the expression of Sp-IAG.
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页数:10
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