Morris J K, Richards J S
Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
J Biol Chem. 1996 Jul 12;271(28):16633-43. doi: 10.1074/jbc.271.28.16633.
The prostaglandin endoperoxide synthase-2 (PGS-2) gene encodes an isoform of prostaglandin synthase that is transiently induced by protein kinase A (luteinizing hormone/cAMP) and protein kinase C (gonadotropin-releasing hormone) agonists in granulosa cells of ovulating follicles. The promoter of the rat PGS-2 gene contains a CAAT enhancer-binding protein consensus site (CAAT box) which can confer hormone inducibility to a PGS-2.CAT reporter gene, as well as a putative E-box region. To determine if the E-box region was involved in hormone induced trans-activation of the rat PGS-2 gene, constructs with the CAAT box and E-box regions (-192 PGS-2.CAT), only the putative E-box (-110 PGS-2.CAT), or neither region (-52 PGS-2.CAT) were transiently transfected into rat granulosa cell cultures. CAT activity was induced in both the -192 and -110 PGS-2*CAT vectors by luteinizing hormone (10-fold) and gonadotropin-releasing hormone (6-fold), whereas CAT activity of the -52 PGS-2.CAT construct did not differ from the promoterless vector (pCAT-Basic). Deletion of 1 base pair from the E-box within the -110 PGS-2.CAT construct, as well as point mutations within the CAAT box, E-box, or both regions of the -192 PGS-2.CAT construct, demonstrated that the E-box is critical for basal transcription, and that regions, in addition to the CAAT box, are involved in hormone induction of the PGS-2 gene. An oligonucleotide spanning the rat PGS-2 E-box bound two specific protein complexes which were supershifted in the presence of antibody specific for the upstream stimulatory factor. Thus, in rat granulosa cells, the PGS-2 E-box region appears to interact with upstream cis-acting elements other than the CAAT box to confer hormonal regulation of the gene. The E-box region of the rat PGS-2 promoter does not contain ATF/CRE activity found in the human and mouse PGS-2 promoters, but is critical for basal transcription of the PGS-2 gene in rat granulosa cells and binds the upstream stimulatory factor (as do E-box regions of other genes regulated in the ovary).
前列腺素内过氧化物合酶-2(PGS-2)基因编码前列腺素合酶的一种同工型,该同工型在排卵卵泡的颗粒细胞中由蛋白激酶A(促黄体生成素/cAMP)和蛋白激酶C(促性腺激素释放激素)激动剂短暂诱导。大鼠PGS-2基因的启动子包含一个CAAT增强子结合蛋白共有位点(CAAT盒),它可赋予PGS-2.CAT报告基因激素诱导性,以及一个假定的E盒区域。为了确定E盒区域是否参与大鼠PGS-2基因的激素诱导的反式激活,将含有CAAT盒和E盒区域(-192 PGS-2.CAT)、仅含有假定的E盒(-110 PGS-2.CAT)或两个区域都不含(-52 PGS-2.CAT)的构建体瞬时转染到大鼠颗粒细胞培养物中。促黄体生成素(10倍)和促性腺激素释放激素(6倍)在-192和-110 PGS-2*CAT载体中均诱导了CAT活性,而-52 PGS-2.CAT构建体的CAT活性与无启动子载体(pCAT-Basic)无差异。从-110 PGS-2.CAT构建体的E盒中缺失1个碱基对,以及-192 PGS-2.CAT构建体的CAAT盒、E盒或两个区域中的点突变,表明E盒对基础转录至关重要,并且除CAAT盒外的区域也参与PGS-2基因的激素诱导。跨越大鼠PGS-2 E盒的寡核苷酸结合了两种特异性蛋白复合物,它们在存在上游刺激因子特异性抗体时发生超迁移。因此,在大鼠颗粒细胞中,PGS-2 E盒区域似乎与CAAT盒以外的上游顺式作用元件相互作用,以赋予该基因激素调节。大鼠PGS-2启动子的E盒区域不包含在人和小鼠PGS-2启动子中发现的ATF/CRE活性,但对大鼠颗粒细胞中PGS-2基因 的基础转录至关重要,并结合上游刺激因子(卵巢中其他受调节基因的E盒区域也是如此)。