Vanselow J, Selimyan R, Fürbass R
Forschungsinstitut für die Biologie landwirtschaftlicher Nutztiere, Wilhelm-Stahl-Allee 2, Dummerstorf, Germany.
Exp Clin Endocrinol Diabetes. 2008 Jul;116(7):437-42. doi: 10.1055/s-2008-1058083. Epub 2008 Apr 1.
Locally produced estrogens are important paracrine regulators of placental growth and differentiation in cattle and sheep. The key enzyme of estrogen biosynthesis, aromatase cytochrome P450, is encoded by CYP19. Transcription of this gene in fetal cotyledons is the first regulatory step of placental estrogen production. The aim of the present study was to comparatively investigate if epigenetic mechanisms as tissue- and differentiation-specific DNA methylation might be involved in the regulation of placental CYP19 expression. Earlier investigations demonstrated that cattle and sheep use different promoters, P1.1 and P1.5 for placental CYP19 expression, respectively. During the present investigation, methylation of individual CpG dinucleotides within these promoter regions was analyzed with bisulfite direct sequencing in placental and luteal tissue. Transcript abundance in sheep was determined with qPCR. Both promoters contain only few CpGs and can therefore be classified as "low CpG densitiy regions". The average methylation levels of both promoter regions were significantly reduced in cotyledons compared to caruncles and corpus luteum of both species, which inversely coincides with high and low expression levels, respectively. It was evident however that even neighbouring CpGs can show very different, individual methylation levels. From the data we conclude that (1) CYP19 promoters are differentially methylated in ovine and bovine placental tissues of foetal and maternal origin; (2) DNA methylation is suggestively involved in the regulation of CYP19 expression; (3) the DNA methylation status on its own is not sufficient for the selection of tissue-and species-specific CYP19 promoters.
局部产生的雌激素是牛和羊胎盘生长与分化的重要旁分泌调节因子。雌激素生物合成的关键酶——芳香化酶细胞色素P450,由CYP19编码。该基因在胎儿子叶中的转录是胎盘雌激素产生的首个调节步骤。本研究的目的是比较研究表观遗传机制,如组织和分化特异性DNA甲基化,是否参与胎盘CYP19表达的调控。早期研究表明,牛和羊分别使用不同的启动子P1.1和P1.5来进行胎盘CYP19的表达。在本研究中,通过亚硫酸氢盐直接测序分析了这些启动子区域内单个CpG二核苷酸在胎盘和黄体组织中的甲基化情况。用qPCR测定绵羊中的转录本丰度。两个启动子仅含有少量CpG,因此可归类为“低CpG密度区域”。与两个物种的肉阜和黄体相比,子叶中两个启动子区域的平均甲基化水平均显著降低,这分别与高表达水平和低表达水平呈负相关。然而,很明显,即使是相邻的CpG也可能表现出非常不同的个体甲基化水平。从数据中我们得出结论:(1)CYP19启动子在胎儿和母体来源的绵羊和牛胎盘组织中存在差异甲基化;(2)DNA甲基化可能参与CYP19表达的调控;(3)DNA甲基化状态本身不足以选择组织和物种特异性的CYP19启动子。