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Tytuł pozycji:

Functional Analysis of Steroidogenic Factor 1 (sf-1) and 17α-Hydroxylase/Lyase (cyp17α) Promoters in Yellow Catfish Pelteobagrus fulvidraco .

Tytuł:
Functional Analysis of Steroidogenic Factor 1 (sf-1) and 17α-Hydroxylase/Lyase (cyp17α) Promoters in Yellow Catfish Pelteobagrus fulvidraco .
Autorzy:
Lv WH; Key Laboratory of Freshwater Animal Breeding, Ministry of Agriculture, Fishery College, Huazhong Agricultural University, Wuhan 430070, China.
Chen GH; Key Laboratory of Freshwater Animal Breeding, Ministry of Agriculture, Fishery College, Huazhong Agricultural University, Wuhan 430070, China.
Zhuo MQ; Key Laboratory of Freshwater Animal Breeding, Ministry of Agriculture, Fishery College, Huazhong Agricultural University, Wuhan 430070, China.
Xu YH; Key Laboratory of Freshwater Animal Breeding, Ministry of Agriculture, Fishery College, Huazhong Agricultural University, Wuhan 430070, China.
Xu YC; Key Laboratory of Freshwater Animal Breeding, Ministry of Agriculture, Fishery College, Huazhong Agricultural University, Wuhan 430070, China.
Tan XY; Key Laboratory of Freshwater Animal Breeding, Ministry of Agriculture, Fishery College, Huazhong Agricultural University, Wuhan 430070, China.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2020 Dec 27; Vol. 22 (1). Date of Electronic Publication: 2020 Dec 27.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Basel, Switzerland : MDPI, [2000-
MeSH Terms:
Promoter Regions, Genetic*
Catfishes/*genetics
Gene Expression Regulation/*genetics
Steroid 17-alpha-Hydroxylase/*genetics
Steroidogenic Factor 1/*genetics
Animals ; Binding Sites ; Catfishes/metabolism ; Cloning, Molecular ; Genes, Reporter ; HEK293 Cells ; Humans ; Leptin/metabolism ; Luciferases/metabolism ; Mutation ; PPAR alpha/genetics ; PPAR alpha/metabolism ; PPAR gamma/genetics ; PPAR gamma/metabolism ; Protein Binding ; STAT3 Transcription Factor/genetics ; STAT3 Transcription Factor/metabolism ; Steroid 17-alpha-Hydroxylase/metabolism ; Steroidogenic Factor 1/metabolism ; Up-Regulation
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Grant Information:
31422056 National Natural Science Foundation of China; 2018YFD0900400 National Key R&D Program of China
Contributed Indexing:
Keywords: Pelteobagrus fulvidraco; cyp17α; sf-1; steroidogenesis; transcriptional regulation
Substance Nomenclature:
0 (Leptin)
0 (PPAR alpha)
0 (PPAR gamma)
0 (STAT3 Transcription Factor)
0 (Steroidogenic Factor 1)
EC 1.13.12.- (Luciferases)
EC 1.14.14.19 (Steroid 17-alpha-Hydroxylase)
Entry Date(s):
Date Created: 20201230 Date Completed: 20210331 Latest Revision: 20210331
Update Code:
20240105
PubMed Central ID:
PMC7795741
DOI:
10.3390/ijms22010195
PMID:
33375507
Czasopismo naukowe
The present study was performed to clone and characterize the structures and functions of steroidogenic factor 1 (sf-1) and 17α-hydroxylase/lyase (cyp17α) promoters in yellow catfish Pelteobagrus fulvidraco , a widely distributed freshwater teleost. We successfully obtained 1981 and 2034 bp sequences of sf-1 and cyp17α promoters, and predicted the putative binding sites of several transcription factors, such as Peroxisome proliferator-activated receptor alpha (PPARα), Peroxisome proliferator-activated receptor gamma (PPARγ) and Signal transducer and activator of transcription 3 (STAT3), on sf-1 and cyp17α promoter regions, respectively. Overexpression of PPARγ significantly increased the activities of sf-1 and cyp17α promoters, but overexpression of PPARα significantly decreased the promoter activities of sf-1 and cyp17α. Overexpression of STAT3 reduced the activity of the sf-1 promoter but increased the activity of the cyp17α promoter. The analysis of site-mutation and electrophoretic mobility shift assay suggested that the sf-1 promoter possessed the STAT3 binding site, but did not the PPARα or PPARγ binding sites. In contrast, only the PPARγ site, not PPARα or STAT3 sites, was functional with the cyp17α promoter. Leptin significantly increased sf-1 promoter activity, but the mutation of STAT3 and PPARγ sites decreased leptin-induced activation of sf-1 promoter. Our findings offered the novel insights into the transcriptional regulation of sf-1 and cyp17α and suggested leptin regulated sf-1 promoter activity through STAT3 site in yellow catfish.
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