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Changes in histone modification and DNA methylation of the StAR and Cyp19a1 promoter regions in granulosa cells undergoing luteinization during ovulation in rats

机译:大鼠排卵过程中黄体化的颗粒细胞中StAR和Cyp19a1启动子区域的组蛋白修饰和DNA甲基化变化

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The ovulatory LH surge induces rapid up-regulation of steroidogenic acute regulatory (StAR) protein and rapid down-regulation of aromatase (Cyp19a1) in granulosa cells (GCs) undergoing luteinization during ovulation. This study investigated in vivo whether epigenetic mechanisms including histone modifications are involved in the rapid changes of StAR and Cyp19a1 gene expression. GCs were obtained from rats treated with equine chorionic gonadotropin (CG) before (0 h) and after human (h)CG injection. StAR mRNA levels rapidly increased after hCG injection, reached a peak at 4h, and then remained higher compared with 0 h until 12 h. Cyp19a1 mRNA levels gradually decreased after hCG injection and reached their lowest level at 12 h. A chromatin immunoprecipitation assay revealed that levels of histone-H4 acetylation (Ac-H4) and trimethylation of histone-H3 lysine-4 (H3K4me3) increased whereas H3K9me3 and H3K27me3 decreased in the StAR promoter after hCG injection. On the other hand, the levels of Ac-H3 and -H4 and H3K4me3 decreased, and H3K27me3 increased in the Cyp19a1 promoter after hCG injection. Chromatin condensation, which was analyzed using deoxyribonuclease I, decreased in the StAR promoter and increased in the Cyp19a1 promoter after hCG injection. A chromatin immunoprecipitation assay also showed that binding activities of CAATT/enhancer-binding protein β to the StAR promoter increased and binding activities of phosphorylated-cAMP response element binding protein to the Cyp19a1 promoter decreased after hCG injection. These results provide in vivo evidence that histone modifications are involved in the rapid changes of StAR and Cyp19a1 gene expression by altering chromatin structure of the promoters in GCs undergoing luteinization during ovulation.
机译:排卵期LH激增导致排卵过程中发生黄体化的颗粒细胞(GCs)中类固醇生成的急性调节(StAR)蛋白快速上调,而芳香化酶(Cyp19a1)迅速下调。这项研究在体内调查包括组蛋白修饰的表观遗传机制是否参与StAR和Cyp19a1基因表达的快速变化。 GCs是从注射人(h)CG之前(0 h)和使用马绒毛膜促性腺激素(CG)处理的大鼠中获得的。 hCG注射后,StAR mRNA水平迅速增加,在4h达到峰值,然后在0h至12h之前保持较高水平。注射hCG后Cyp19a1 mRNA水平逐渐下降,并在12h达到最低水平。染色质免疫沉淀试验显示,在注射hCG后,StAR启动子中组蛋白H4乙酰化(Ac-H4)和组蛋白H3赖氨酸4(H3K4me3)的三甲基化水平升高,而H3K9me3和H3K27me3降低。另一方面,hCG注射后,Cyp19a1启动子中Ac-H3和-H4和H3K4me3的水平降低,而H3K27me3的水平升高。注射hCG后,使用脱氧核糖核酸酶I分析的染色质凝聚在StAR启动子中减少,在Cyp19a1启动子中增加。染色质免疫沉淀试验还显示,hCG注射后,CAATT /增强子结合蛋白β与StAR启动子的结合活性增加,磷酸化cAMP反应元件结合蛋白与Cyp19a1启动子的结合活性降低。这些结果提供了体内证据,表明通过在排卵过程中发生黄体化的GC中,通过改变启动子的染色质结构,组蛋白修饰与StAR和Cyp19a1基因表达的快速变化有关。

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