De Luca L M
Laboratory of Cellular Carcinogenesis and Tumor Promotion, National Cancer Institute, Bethesda, Maryland 20892.
FASEB J. 1991 Nov;5(14):2924-33.
The crucial role of retinoids in controlling differentiation processes has become evident from studies conducted in a variety of in vivo and in vitro systems. Most striking is the role of retinoic acid as a morphogenic substance in vertebrate limb development, but equally important is its role in the maintenance of epithelial integrity in most superficial linings of the body. The similarity of the mode of action of retinoids to that of the steroid and thyroid hormones has recently been demonstrated with the discovery of the nuclear receptors for retinoic acid, which belong to the steroid/thyroid hormone receptor superfamily. These receptors act as transcriptional activators by binding as heterodimers to specific nucleotide sequences in the response elements of target genes. Response elements for retinoic acid have so far been identified for the rat growth hormone and phosphoenolpyruvate carboxykinase, the mouse complement H and laminin B1, the human and mouse retinoic acid receptor beta, the human osteocalcin, and the human alcohol dehydrogenase genes. The retinoic acid response element (RARE) for the rat growth hormone gene is also a thyroid hormone response element (TRE), and the AP-1 binding site of the human osteocalcin promoter is also a vitamin D response element (VDRE) and a RARE. Both these elements are palindromic. Other RAREs have a direct repeat configuration of the half-site motif AGGTCA separated by five nucleotides (AGGTCA xxxxx AGGTCA). The direct repeat arrangement of the same core motif AGGTCA separated by three or four nucleotides becomes a VDRE or TRE, respectively. A point mutation has been identified in the RAR alpha gene of embryonal carcinoma cells resistant to retinoic acid. In addition to the three retinoic acid receptors (alpha, beta, gamma) belonging to the steroid/thyroid hormone receptor superfamily, a second class of retinoid receptors (RXR) alpha, beta, gamma has also been characterized and its relatedness to a gene, XR2C, of the locus ultraspiracle required for pattern formation in Drosophila has been established. That would suggest that both vertebrates and invertebrates may require similar transcriptional activators during morphogenesis. An RXRE has been identified in the CRBPII gene promoter and it contains five repeats of the canonical sequence AGGTCA separated by one nucleotide. The importance of retinoids, both as chemopreventive agents of tumorigenesis and potent differentiation inducers of neoplastic cells, can only be emphasized by the recent finding that the t(15;17) (q21- q11-22) translocation, specifically associated with acute promyelocytic leukemia, also causes translocation of the retinoic acid receptor alpha gene and its fusion with with a new locus, myl, of unknown function.(ABSTRACT TRUNCATED AT 250 WORDS)
视黄酸在控制分化过程中的关键作用已在多种体内和体外系统的研究中得以显现。最显著的是视黄酸在脊椎动物肢体发育中作为形态发生物质的作用,但其在维持身体大多数表层上皮完整性方面的作用同样重要。随着视黄酸核受体的发现,视黄酸的作用模式与类固醇和甲状腺激素的作用模式相似性得以证实,视黄酸核受体属于类固醇/甲状腺激素受体超家族。这些受体通过以异二聚体形式结合到靶基因反应元件中的特定核苷酸序列上,充当转录激活剂。到目前为止,已鉴定出大鼠生长激素和磷酸烯醇丙酮酸羧激酶、小鼠补体H和层粘连蛋白B1、人和小鼠视黄酸受体β、人骨钙素以及人乙醇脱氢酶基因的视黄酸反应元件。大鼠生长激素基因的视黄酸反应元件(RARE)也是甲状腺激素反应元件(TRE),人骨钙素启动子的AP - 1结合位点也是维生素D反应元件(VDRE)和RARE。这两个元件都是回文结构。其他RARE具有由五个核苷酸隔开的半位点基序AGGTCA 的直接重复结构(AGGTCA xxxxx AGGTCA)。由三个或四个核苷酸隔开的相同核心基序AGGTCA的直接重复排列分别成为VDRE或TRE。在对视黄酸耐药的胚胎癌细胞的RARα基因中已鉴定出一个点突变。除了属于类固醇/甲状腺激素受体超家族的三种视黄酸受体(α、β、γ)外,第二类视黄酸受体(RXR)α、β、γ也已被鉴定,并且已确定其与果蝇模式形成所需的超气门基因座的一个基因XR2C的相关性。这表明脊椎动物和无脊椎动物在形态发生过程中可能需要相似的转录激活剂。在CRBPII基因启动子中已鉴定出一个RXRE,它包含由一个核苷酸隔开的规范序列AGGTCA的五个重复。视黄酸作为肿瘤发生的化学预防剂和肿瘤细胞的有效分化诱导剂的重要性,只能通过最近的一项发现来强调,即与急性早幼粒细胞白血病特异性相关的t(15;17) (q21 - q11 - 22)易位,也导致视黄酸受体α基因易位并与一个功能未知的新基因座myl融合。(摘要截短至250字)