Dussault I, Giguère V
Department of Medicine, McGill University, Montréal, Québec, Canada.
Mol Cell Biol. 1997 Apr;17(4):1860-7. doi: 10.1128/MCB.17.4.1860.
ROR alpha1 and RVR are orphan members of the superfamily of nuclear hormone receptors which constitutively activate and repress, respectively, gene transcription by binding to a common DNA sequence. In an attempt to understand the physiological functions of these two transcription factors, we aimed to identify target genes. We have identified a consensus binding site for ROR alpha1 and RVR in the first intron of the N-myc gene that we designated N-myc RORE (ROR response element). Unlike most of the intronic sequence, the region encompassing the N-myc RORE is highly conserved between human and mouse, underscoring its importance. Our studies revealed that ROR alpha1 and RVR specifically bind to the human and mouse N-myc ROREs and transactivate and transrepress, respectively, reporter constructs containing the ROREs. Moreover, Northern blot analysis demonstrated a direct modulation of an exogenously introduced N-myc gene by ROR alpha1 and RVR in COS-1 cells. This effect is mediated through the N-myc RORE, since mutation of this site abolished the regulatory effects of both receptors. While transfection of ROR alpha1 in P19 embryonic carcinoma cells had no effect on the levels of endogenous N-myc mRNA, RVR down-regulated its expression. The regulatory function of the N-myc RORE was further demonstrated by the rat embryonic fibroblast (REF) transformation assay. Mutation of the RORE increased the oncogenic potential of the N-myc gene in the REF assay. The foci were more numerous and significantly larger with the mutated than with the wild-type N-myc gene, regardless of ROR alpha1 or RVR expression. Moreover, concomitant expression of ROR alpha1 and wild-type N-myc resulted in a twofold increase in the number of transformed foci. In contrast, RVR expression resulted in the formation of foci that could be established as permanent clones with a very low frequency compared to foci transformed in its absence. These observations show that ablation of the RORE results in a more oncogenic form of N-myc and suggest that deregulation of the activity of the ROR alpha1 and RVR could contribute to the initiation and progression of certain neoplasias.
RORα1和RVR是核激素受体超家族的孤儿成员,它们分别通过与共同的DNA序列结合来组成性地激活和抑制基因转录。为了了解这两种转录因子的生理功能,我们旨在鉴定靶基因。我们在N - myc基因的第一个内含子中鉴定出了一个RORα1和RVR的共有结合位点,我们将其命名为N - myc RORE(ROR反应元件)。与大多数内含子序列不同,包含N - myc RORE的区域在人和小鼠之间高度保守,这突出了其重要性。我们的研究表明,RORα1和RVR特异性地结合人和小鼠的N - myc RORE,并分别激活和抑制含有RORE的报告基因构建体。此外,Northern印迹分析表明,RORα1和RVR在COS - 1细胞中对外源引入的N - myc基因有直接调节作用。这种效应是通过N - myc RORE介导的,因为该位点的突变消除了两种受体的调节作用。虽然在P19胚胎癌细胞中转染RORα1对内源N - myc mRNA水平没有影响,但RVR下调了其表达。大鼠胚胎成纤维细胞(REF)转化试验进一步证明了N - myc RORE的调节功能。RORE的突变增加了N - myc基因在REF试验中的致癌潜力。无论RORα1或RVR的表达如何,与野生型N - myc基因相比,突变型N - myc基因形成的病灶更多且明显更大。此外,RORα1和野生型N - myc的共表达导致转化病灶数量增加两倍。相比之下,RVR的表达导致形成的病灶能够以极低的频率建立为永久克隆,而在没有RVR表达的情况下转化的病灶则不然。这些观察结果表明,RORE的缺失导致N - myc形成更具致癌性的形式,并表明RORα1和RVR活性的失调可能有助于某些肿瘤的发生和发展。