Department of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
J Neurochem. 2011 Oct;119(1):6-17. doi: 10.1111/j.1471-4159.2011.07397.x. Epub 2011 Aug 22.
Arylalkylamine N-acetyltransferase (AANAT) is the key regulatory enzyme controlling the daily rhythm of melatonin biosynthesis. In chicken retinal photoreceptor cells, Aanat transcription and AANAT activity are regulated in part by cAMP-dependent mechanisms. The purpose of this study was to identify regulatory elements within the chicken Aanat promoter responsible for cAMP-dependent induction. Photoreceptor-enriched retinal cell cultures were transfected with a luciferase reporter construct containing up to 4 kb of 5'-flanking region and the first exon of Aanat. Forskolin treatment stimulated luciferase activity driven by the ∼4 kb promoter construct and by all 5'-deletion constructs except the smallest, Aanat (-217 to +120)luc. Maximal basal and forskolin-stimulated expression levels were generated by the Aanat (-484 to +120)luc construct. This construct lacks a canonical cyclic AMP-response element (CRE), but contains two other potentially important elements in its sequence: an eight times TTATT repeat (TTATT₈) and a CRE-like sequence. Electrophoretic mobility shift assays, luciferase reporter assays, chromatin immunoprecipitation, and siRNA experiments provide evidence that these elements bind c-Fos, JunD, and CREB to enhance basal and forskolin-stimulated Aanat transcription. We propose that the CRE-like sequence and TTATT₈ elements in the 484 bp proximal promoter interact to mediate cAMP-dependent transcriptional regulation of Aanat.
芳香族烷基胺 N-乙酰基转移酶(AANAT)是控制褪黑素生物合成日节律的关键调节酶。在鸡视网膜光感受器细胞中,Aanat 转录和 AANAT 活性部分受到 cAMP 依赖性机制的调节。本研究的目的是鉴定鸡 Aanat 启动子内负责 cAMP 依赖性诱导的调节元件。用包含多达 4kb5'-侧翼区和 Aanat 第一外显子的荧光素酶报告基因构建体转染富含光感受器的视网膜细胞培养物。forskolin 处理刺激由约 4kb 启动子构建体和所有 5'-缺失构建体(除最小的 Aanat(-217 至+120)luc 外)驱动的荧光素酶活性。Aanat(-484 至+120)luc 构建体产生最大的基础和 forskolin 刺激表达水平。该构建体缺乏规范的环 AMP 反应元件(CRE),但其序列中包含另外两个潜在重要的元件:八次 TTATT 重复(TTATT₈)和 CRE 样序列。电泳迁移率变动分析、荧光素酶报告基因分析、染色质免疫沉淀和 siRNA 实验提供的证据表明,这些元件结合 c-Fos、JunD 和 CREB,以增强基础和 forskolin 刺激的 Aanat 转录。我们提出,484bp 近端启动子中的 CRE 样序列和 TTATT₈ 元件相互作用,介导 Aanat 的 cAMP 依赖性转录调节。