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芳香化酶抑制剂对暗纹东方鲀CYP19A、DMRT1基因表达及性腺分化的影响
引用本文:黄波,杨小玉,戴奇,汪奇,云丹,周忠良.芳香化酶抑制剂对暗纹东方鲀CYP19A、DMRT1基因表达及性腺分化的影响[J].中国水产科学,2013,20(1):68-74.
作者姓名:黄波  杨小玉  戴奇  汪奇  云丹  周忠良
作者单位:1. 华东师范大学 生命科学学院, 上海 200062
2. 江苏中润农业发展有限公司, 江苏 南通 226634
基金项目:上海自然科学基金(08ZR1407300)
摘    要:采用组织学和分子生物学方法,研究了投喂芳香化酶抑制剂来曲唑(LE)后暗纹东方鲀(Takifugu obscures)初孵仔鱼CYP19A、DMRT1基因表达以及性腺的组织学变化,以期进一步了解P450芳香化酶(P450arom)在鱼类早期性别分化过程中的作用。RT-PCR结果显示,对照组样品CYP19A和DMRT1表达显示性二态,雌性表达CYP19A基因,雄性表达DMRT1基因。LE处理组在性别分化期间,雄性样品单一表达DMRT1,雌性样品则同时表达CYP19A和DMRT1。qRT-PCR结果显示:LE处理组雌性仔鱼CYP19A基因表达被显著抑;虽然在仔鱼出膜后22d(dph)的表达水平高于9 dph,但仅为同日对照组的2.11%。LE处理组雌性样品22 dph时DMRT1基因表达量上调,至150 dph时达对照组雄性水平。55 dph的性腺组织学结果表明,LE处理可导致暗纹东方鲀稚鱼原始卵巢退化,并向功能性精巢发育。150 dph的LE处理组性腺均为精巢,并与对照组精巢发育同步。结论认为,暗纹东方鲀性腺分化期间P450arom是卵巢形成和维持发育所必须的,抑制P450arom活性可导致雌性暗纹东方鲀发生雄性化逆转。

关 键 词:暗纹东方鲀  性别分化  芳香化酶抑制剂(AI)  CYP19A  DMRT1
修稿时间:2013/2/20 0:00:00

Effect of aromatase inhibitor on expression of CYP19A, DMRT1, and gonadal sex differentiation in Takifugu obscures
HUANG Bo,YANG Xiaoyu,DAI Qi,WANG Qi,YUN Dan,ZHOU Zhongliang.Effect of aromatase inhibitor on expression of CYP19A, DMRT1, and gonadal sex differentiation in Takifugu obscures[J].Journal of Fishery Sciences of China,2013,20(1):68-74.
Authors:HUANG Bo  YANG Xiaoyu  DAI Qi  WANG Qi  YUN Dan  ZHOU Zhongliang
Institution:1.School of Life Science,East China Normal University,Shanghai 200062,China; 2.Jang Su Zhong Run Agricultural Development Co.,Ltd.,Nantong 226634,China
Abstract:As in all other lower vertebrates, sex differentiation in fish is susceptible to environmental and steroidogenic stimulation or inhibition. Alteration of the sex differentiation process is possible in many fishes through the manipulation of the environment and steroid function. Some chemicals, which have androgenic or estrogenic function, are known to alter the gonadal sex in fish from female to male or vice versa if administered during the period of gonadal sex differentiation. Other than direct androgenic or estrogenic effects, there are chemicals which are capable of disrupting the enzymatic pathway of natural androgenic-estrogenic balance in fish. Among the non-steroidal aromatase inhibitors (AI), letrozole is typically used as an effective human drug in the treatment of estrogen-dependent disease, including breast cancer, and was found to be effective in suppression of all estrogens after oral administration. )]. Gonadal development was observed histologically using a microscope, and the expression of CYP19A and CYP19A was expressed in female, and A quantitative real-time PCR analysis revealed that the expression of the gene in female was significantly inhibited after treatment with LE. Though expression of was higher at 22 days post hatch (dph) than at 9 dph, it was only 2.11 the level of the control female. gene expression was up-regulated gradually in LE treated female fry during sex differentiation, and reached the same level as control males at 150 dph. In LE treated female fry, degeneration of the ovarian cavity and primary spermatocytes were observed in sections of the gonad. The functional testes were developed at 150 dph. Our research demonstrates that aromatase activity is necessary for ovarian formation and development during sex differentiation in T. obscures during sex differentiation.
Keywords:Takifugu obscures  sex differentiation  aromatase inhibitor AI  CYP19A  DMRT1
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