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Molecular mechanism of feedback regulation of 17β‐estradiol on two kiss genes in the protogynous orange‐spotted grouper ( Epinephelus coioides )
Author(s) -
Guo Yin,
Wang Qingqing,
Li Gaofei,
He Meng,
Tang Haipei,
Zhang Haifa,
Yang Xiaoli,
Liu Xiaochun,
Lin Haoran
Publication year - 2017
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/mrd.22800
Subject(s) - biology , grouper , kisspeptin , promoter , medicine , endocrinology , microbiology and biotechnology , estrogen receptor , genetics , gene , gene expression , hypothalamus , fishery , cancer , breast cancer , fish <actinopterygii>
Kisspeptins are considered critical regulators in the hypothalamic‐pituitary‐gonadal axis because they can stimulate secretion of Gonadotropin‐releasing hormone in mammals, and may also mediate the feedback regulation of sex steroids in the hypothalamus. Two kiss1 paralogues ( kiss1 and kiss2 ) were identified in teleosts, hinting at their increased complexity of signaling for sex‐steroid feedback regulation. In the present study, molecular pathways by which 17β‐estradiol (E 2 ) exerted feedback regulation on two kiss genes, via three types of estrogen receptors, were investigated in the protogynous orange‐spotted grouper ( Epinephelus coioides ). kiss2 expression in the brain significantly increased in ovariectomized orange‐spotted groupers, while E 2 replacement in ovariectomized fish reversed these changes to levels in the sham‐surgery group; conversely, kiss1 expression did not change. Dual‐label in situ hybridization showed that kiss1 and kiss2 neurons express erα , erβ1 , and erβ2 , indicating that E 2 may directly regulate kiss1 and kiss2 . Indeed, E 2 treatment of transiently transfected HEK293T cells decreased the activity of both kiss promoters in the presence of erβ1 and erβ2 rather than erα . Further deletion and site‐directed mutagenesis of the kiss promoters indicated that kiss1 is regulated by E 2 via an estrogen‐responsive element (ERE)‐dependent, classical pathway utilized by Erβ1, as well as via an Activator protein 1 (Ap1)‐dependent, non‐classical pathway utilized by Erβ2. kiss2 was also differently regulated by E 2 through the Creb transcription factor, utilized by Erβ1 as well as a half‐ERE‐dependent, classical pathway utilized by Erβ2. Taken together, multiple signaling pathways in orange‐spotted grouper are clearly involved in the feedback regulation of E 2 on kiss genes via different estrogen receptors.