Tissue-specific promoters regulate the transcription of cyp19a1 in the brain-pituitary-gonad axis of Japanese eel (Anguilla japonica).


Journal

The Journal of steroid biochemistry and molecular biology
ISSN: 1879-1220
Titre abrégé: J Steroid Biochem Mol Biol
Pays: England
ID NLM: 9015483

Informations de publication

Date de publication:
09 2023
Historique:
received: 13 02 2023
revised: 16 05 2023
accepted: 22 05 2023
medline: 25 8 2023
pubmed: 27 5 2023
entrez: 26 5 2023
Statut: ppublish

Résumé

Aromatase is a key enzyme that catalyzes the biosynthesis of estrogens. Previous study indicated that putative tissue-specific promoters of the one aromatase gene (cyp19a1) may drive the differential regulatory mechanisms of cyp19a1 expression in Anguilla japonica. In the present study, for elucidating the transcription characteristics and the function of putative tissue-specific promoters of cyp19a1 in the brain-pituitary-gonad (BPG) axis during vitellogenesis, we investigated the transcriptional regulation of cyp19a1 by 17β-estrogen (E2), testosterone (T), or human chorionic gonadotropin (HCG) in A. japonica. The expression of estrogen receptor (esra), androgen receptor (ara), or luteinizing hormone receptor (lhr) was up-regulated as cyp19a1 in response to E2, T, or HCG, respectively in the telencephalon, diencephalon, and pituitary. The expression of cyp19a1 was also upregulated in the ovary by HCG or T in a dose-dependent manner. Unlike in the brain and pituitary, the expression of esra and lhr, rather than ara, was upregulated by T in the ovary. Subsequently, four primary subtypes of 5'-untranslated terminal regions of cyp19a1 transcripts and the corresponding two 5' flanking regions (promoter P.I and P.II) were identified. The P.II existed in all BPG axis tissues, whereas the P.I with strong transcriptional activity was brain- and pituitary-specific. Furthermore, the transcriptional activity of promoters, the core promoter region, and the three putative hormone receptor response elements were validated. The transcriptional activity did not change when the HEK291T cells co-transfected with P.II and ar vector were exposed to T. These results suggested that the expression of cyp19a1 was upregulated indirectly through esra and lhr rather than ara by T in the ovary, whereas the expression of cyp19a1 was upregulated directly through androgen receptor and the downstream androgen response element of tissue-specific P.I in the brain and pituitary. The results of the study reveal the regulatory mechanisms of estrogen biosynthesis and provide a reference for optimizing the technology of artificially induced maturation in eels.

Identifiants

pubmed: 37236374
pii: S0960-0760(23)00089-4
doi: 10.1016/j.jsbmb.2023.106334
pii:
doi:

Substances chimiques

Aromatase EC 1.14.14.1
Receptors, Androgen 0
Cytochrome P-450 CYP1A1 EC 1.14.14.1
Estrogens 0
Receptors, Estrogen 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106334

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that there is no conflict of competing interest.

Auteurs

Xiaojian Lai (X)

Fisheries College, Jimei University, Xiamen 361021, China; Engineering Research Center of the Modern Technology for Eel Industry, Ministry of Education P. R. China, Xiamen 361021, China. Electronic address: laixj@jmu.edu.cn.

Shuai Peng (S)

Fisheries College, Jimei University, Xiamen 361021, China.

Liping Liu (L)

College of Fisheries and Life Science, Shanghai Ocean University, Shanghai 201306, China.

Zhihua Zou (Z)

Fisheries College, Jimei University, Xiamen 361021, China.

Le Cao (L)

Fisheries College, Jimei University, Xiamen 361021, China; Engineering Research Center of the Modern Technology for Eel Industry, Ministry of Education P. R. China, Xiamen 361021, China.

Yilei Wang (Y)

Fisheries College, Jimei University, Xiamen 361021, China. Electronic address: ylwang@jmu.edu.cn.

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Classifications MeSH