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Runt-Related Transcription Factor 1 Regulates Luteinized Hormone-Induced Prostaglandin-Endoperoxide Synthase 2 Expression in Rat Periovulatory Granulosa Cells

机译:矮子相关转录因子1调节黄素化激素诱导的前列腺素内过氧化物合酶2在大鼠排卵性颗粒细胞中的表达。

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摘要

Runt-related transcription factor 1 (RUNX1), a transcription factor, is transiently induced by the LH surge and regulates gene expression in periovulatory granulosa cells. Potential binding sites for RUNX are present in the 5′-flanking region of the Ptgs2 (prostaglandin-endoperoxide synthase 2) gene. Periovulatory Ptgs2 expression is essential for ovulation. In the present study, we investigated the role of RUNX1 in mediating the LH-induced expression of Ptgs2 in periovulatory granulosa cells. We first determined whether the suppression of Runx1 expression or activity affects Ptgs2 expression using cultured preovulatory granulosa cells isolated from immature rat ovaries primed with pregnant mare serum gonadotropin for 48 h. Knockdown of human chorionic gonadotropin-induced Runx1 expression by small interfering RNA or inhibition of endogenous RUNX activities by dominant-negative RUNX decreased human chorionic gonadotropin or agonist-stimulated Ptgs2 expression and transcriptional activity of Ptgs2 promoter reporter constructs. Results from chromatin immunoprecipitation assays revealed in vivo binding of endogenous RUNX1 to the Ptgs2 promoter region in rat periovulatory granulosa cells. Direct binding of RUNX1 to two RUNX-binding motifs in the Ptgs2 promoter region was confirmed by EMSA. The mutation of these two binding motifs resulted in decreased transcriptional activity of Ptgs2 promoter reporter constructs in preovulatory granulosa cells. Taken together, these findings provide experimental evidence that the LH-dependent induction of Ptgs2 expression results, in part, from RUNX1-mediated transactivation of the Ptgs2 promoter. The results of the present study assign potential significance for LH-induced RUNX1 in the ovulatory process via regulating Ptgs2 gene expression.
机译:矮小相关转录因子1(RUNX1)是一种转录因子,由LH激增短暂诱导,并调节排卵性颗粒细胞中的基因表达。 RUNX的潜在结合位点存在于Ptgs2(前列腺素-内过氧化物合酶2)基因的5'侧翼区域。围排卵期Ptgs2表达对于排卵至关重要。在本研究中,我们调查了RUNX1在介导LH诱导的排卵性颗粒细胞中Ptgs2表达中的作用。我们首先确定了Runx1表达或活性的抑制是否影响Ptgs2表达,使用培养的排卵前颗粒细胞从孕母马血清促性腺激素引发的未成熟大鼠卵巢中分离48 h。通过小的干扰RNA抑制人绒毛膜促性腺激素诱导的Runx1表达或通过显性负性RUNX抑制内源性RUNX活性降低了人绒毛膜促性腺激素或激动剂刺激的Ptgs2表达和Ptgs2启动子报告基因构建体的转录活性。染色质免疫沉淀试验的结果表明,内源性RUNX1与大鼠排卵性颗粒细胞中Ptgs2启动子区域的体内结合。 EMSA证实了RUNX1与Ptgs2启动子区域中两个RUNX结合基序的直接结合。这两个结合基序的突变导致排卵前颗粒细胞中Ptgs2启动子报告基因构建体的转录活性降低。综上所述,这些发现提供了实验证据,即LH依赖的Ptgs2表达的诱导部分是由RUNX1介导的Ptgs2启动子的反式激活引起的。本研究的结果通过调节Ptgs2基因表达为排卵过程中LH诱导的RUNX1赋予了潜在的意义。

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