Young Joyce E, Vogt Todd, Gross Kenneth W, Khani Shahrokh C
Department of Ophthalmology and Biochemistry, State University of New York at Buffalo, New York 14215, USA.
Invest Ophthalmol Vis Sci. 2003 Sep;44(9):4076-85. doi: 10.1167/iovs.03-0197.
Rhodopsin kinase (Rk or GRK1) is a photoreceptor-specific enzyme that mediates adaptation of photoreceptors to light and protects these cells against light-induced injury. This study examined the transcriptional mechanisms that maintain physiologic levels of this essential enzyme in photoreceptors.
The 2.0-kb region flanking the 5' end of the human Rk gene was isolated, mapped, and sequenced. The sequence was fused upstream of the luciferase gene and was tested for promoter activity in retinoblastoma cells by transient transfection. Transcriptionally active segments were identified by deletion and site-directed mutagenesis. Transgenic mice were generated that carried the immediate 5' flanking segment linked upstream of the enhancerless green fluorescent protein (GFP) gene. GFP expression was analyzed by RT-PCR, fluorescence microscopy, and immunohistochemistry.
Mapping and sequence analysis uncovered a TATA-less promoter with several recognizable elements concentrated proximally. A conserved putative homeodomain response element H1 and a GC- and a GA-rich motif were noted within a 0.11-kb region. Another putative homeodomain binding site, H2, and a stretch of C-rich repeats were present distally. Mutagenesis in conjunction with transient transfection in retinoblastoma cells identified the 0.11-kb region and H1 sequence as the key active enhancer-promoter sequences. The distal sequences were inhibitory. Transgenic mice that carried the 0.11-kb DNA segment with the GFP gene linked downstream showed GFP transcript, fluorescence, and immunoreactivity that were restricted to photoreceptors.
The experiments defined a short, highly active photoreceptor-specific enhancer-promoter region upstream of the Rk gene. The H1 element contributed substantially but not exclusively to the transcriptional activity of the region. The findings support a transcriptional basis for photoreceptor-specific expression of Rk.
视紫红质激酶(Rk或GRK1)是一种光感受器特异性酶,介导光感受器对光的适应,并保护这些细胞免受光诱导的损伤。本研究探讨了维持光感受器中这种必需酶生理水平的转录机制。
分离、定位并测序了人Rk基因5'端侧翼的2.0 kb区域。该序列与荧光素酶基因上游融合,并通过瞬时转染在视网膜母细胞瘤细胞中检测其启动子活性。通过缺失和定点诱变鉴定转录活性片段。构建了转基因小鼠,其携带与无增强子绿色荧光蛋白(GFP)基因上游相连的紧邻5'侧翼片段。通过RT-PCR、荧光显微镜和免疫组织化学分析GFP表达。
定位和序列分析发现一个无TATA的启动子,几个可识别元件集中在近端。在0.11 kb区域内发现了一个保守的假定同源结构域反应元件H1以及一个富含GC和GA的基序。在远端存在另一个假定的同源结构域结合位点H2和一段富含C的重复序列。在视网膜母细胞瘤细胞中进行诱变并结合瞬时转染,确定0.11 kb区域和H1序列为关键的活性增强子-启动子序列。远端序列具有抑制作用。携带与GFP基因下游相连的0.11 kb DNA片段的转基因小鼠显示GFP转录本、荧光和免疫反应性仅限于光感受器。
实验确定了Rk基因上游一个短的、高活性的光感受器特异性增强子-启动子区域。H1元件对该区域的转录活性有很大贡献,但不是唯一的贡献。这些发现支持了Rk光感受器特异性表达的转录基础。