Hashemain Zohreh, Amiri-Yekta Amir, Khosravifar Mona, Alvandian Faezeh, Shahhosseini Maryam, Hosseinkhani Saman, Afsharian Parvaneh
Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Human and Animal Cell Bank, Iranian Biological Resource Center (IBRC), ACECR, Tehran, Iran.
Cell J. 2022 Apr;24(4):170-175. doi: 10.22074/cellj.2022.7787. Epub 2022 Apr 27.
Estrogen, a female hormone maintaining several critical functions in women's physiology, e.g., folliculogenesis and fertility, is predominantly produced by ovarian granulosa cells where aromatase enzyme converts androgen to estrogen. The principal enzyme responsible for this catalytic reaction is encoded by the gene, with a long regulatory region. Abnormalities in this process cause metabolic disorders in women, one of the most common of which is polycystic ovary syndrome (PCOS). The main purpose of this research was to determine the effect of the promoters on aromatase expression in cells with normal and PCOS characteristics.
In this experimental study, four promoters of the gene, including PII, I.3, I.4, and PII/ I .3 promoter fragments, were cloned upstream of the luciferase gene and transfected into normal and PCOS granulosa cells. Subsequently, the effect of follicle-stimulating hormone (FSH) on the activity of these regulatory regions was examined in the presence and absence of FSH. Western blotting was used to confirm aromatase expression in all groups. Data analysis was performed using ANOVA and paired sample t test, compared by post-hoc least significant difference (LSD) test.
Luciferase results confirmed the intense activity of PII promoter in the presence of FSH. Moreover, the study demonstrated reduced activity of PII promoter in normal granulosa cells, possibly due to the regulatory region of I.3 next to PII.
FSH stimulates transcription of aromatase enzyme by affecting PII promoter, a process regulated by the inhibitory role of the I.3 region in PII activity in granulosa cells. Given the distinct role of these promoters in normal and PCOS granulosa cells, the importance of nuclear factors residing in these regions can be discerned.
雌激素是一种在女性生理过程中维持多种关键功能的女性激素,例如卵泡发生和生育能力,主要由卵巢颗粒细胞产生,在该细胞中芳香化酶将雄激素转化为雌激素。负责这种催化反应的主要酶由该基因编码,其具有一个长的调控区域。这一过程中的异常会导致女性代谢紊乱,其中最常见的一种是多囊卵巢综合征(PCOS)。本研究的主要目的是确定这些启动子对具有正常和PCOS特征的细胞中芳香化酶表达的影响。
在本实验研究中,该基因的四个启动子,包括PII、I.3、I.4以及PII/I.3启动子片段,被克隆到荧光素酶基因的上游,并转染到正常和PCOS颗粒细胞中。随后,在有和没有促卵泡激素(FSH)的情况下,检测FSH对这些调控区域活性的影响。采用蛋白质免疫印迹法来确认所有组中芳香化酶的表达。数据分析采用方差分析和配对样本t检验,并通过事后最小显著差异(LSD)检验进行比较。
荧光素酶结果证实了PII启动子在FSH存在时具有强烈活性。此外,该研究表明正常颗粒细胞中PII启动子的活性降低,这可能是由于紧邻PII的I.3调控区域所致。
FSH通过影响PII启动子来刺激芳香化酶的转录,这一过程受到颗粒细胞中I.3区域对PII活性的抑制作用的调控。鉴于这些启动子在正常和PCOS颗粒细胞中的不同作用,可以看出这些区域中核因子的重要性。