Brown P, Mcneilly A S
MRC Reproductive Biology Unit, Centre for Reproductive Biology, Edinburgh, U.K.
Int J Biochem Cell Biol. 1997 Dec;29(12):1513-24. doi: 10.1016/s1357-2725(97)00082-4.
Luteinising hormone (LH) and follicle stimulating hormone (FSH) comprise a common alpha-subunit and hormone-specific beta-subunit, are expressed in gonadotroph cells of the anterior pituitary and during the sheep oestrous cycle, are regulated by gonadotrophin releasing hormone (GnRH), ovarian peptides and steroids. Transcription factor steroidogenic factor-1 (SF-1) transactivates the common alpha-subunit and LH beta subunit in other species. We investigated whether SF-1 regulates beta-subunit expression and the regulation of SF-1 expression in vivo in sheep. Immunocytochemistry co-localised SF-1, LH and FSH to sheep pituitary gonadotrophs and electrophoretic mobility shift assays (EMSA) demonstrated that SF-1 bound to the LH beta promoter in vitro. No SF-1 DNA binding site was found in the FSH beta promoter. No difference in mean levels of SF-1, FSH beta, LH beta and GnRHr mRNA was measured between the luteal and follicular phases of the oestrous cycle. However SF-1 mRNA levels were correlated to those of LH beta in individual luteal phase animals (r = 0.88, p < 0.05), when the transcription rate of LH beta was significantly higher (p < 0.01). GnRH antagonist treatment of luteal animals did not produce a significant reduction in mRNA levels of LH beta, SF-1 and FSH beta. Administering oestradiol benzoate with GnRH antagonist reduced levels of SF-1 and FSH beta mRNA from luteal values (p < 0.005). We conclude that: (1) expression of SF-1 is not solely dependent on GnRH and is downregulated by oestradiol; (2) the LH beta transcription rate is increased during the luteal phase but is not related to levels of LH beta or SF-1 mRNA; and (3) SF-1 does not appear to directly regulate expression of FSH beta, but may regulate expression indirectly.
促黄体生成素(LH)和促卵泡生成素(FSH)由一个共同的α亚基和激素特异性β亚基组成,在前脑垂体的促性腺细胞中表达,并且在绵羊发情周期中受促性腺激素释放激素(GnRH)、卵巢肽和类固醇的调节。转录因子类固醇生成因子-1(SF-1)可在其他物种中反式激活共同的α亚基和LHβ亚基。我们研究了SF-1是否在绵羊体内调节β亚基表达以及SF-1表达的调控。免疫细胞化学将SF-1、LH和FSH共定位于绵羊垂体促性腺细胞,电泳迁移率变动分析(EMSA)表明SF-1在体外与LHβ启动子结合。在FSHβ启动子中未发现SF-1 DNA结合位点。在发情周期的黄体期和卵泡期之间,未检测到SF-1、FSHβ、LHβ和GnRHr mRNA的平均水平存在差异。然而,在个体黄体期动物中,当LHβ的转录率显著更高时(p<0.01),SF-1 mRNA水平与LHβ的水平相关(r = 0.88,p<0.05)。对黄体期动物进行GnRH拮抗剂处理并未使LHβ、SF-1和FSHβ的mRNA水平显著降低。用GnRH拮抗剂给予苯甲酸雌二醇可使SF-1和FSHβ mRNA水平从黄体期值降低(p<0.005)。我们得出以下结论:(1)SF-1的表达不仅依赖于GnRH,且受雌二醇下调;(2)LHβ转录率在黄体期增加,但与LHβ或SF-1 mRNA水平无关;(3)SF-1似乎不直接调节FSHβ的表达,但可能间接调节表达。