Lin C S, Chow S, Lau A, Tu R, Lue T F
Knuppe Molecular Urology Laboratory, Department of Urology, School of Medicine, University of California, San Francisco, California 94143-1695, USA.
Biochem Biophys Res Commun. 2001 Jan 26;280(3):684-92. doi: 10.1006/bbrc.2000.4220.
PDE5A gene encodes type 5 phosphodiesterase (PDE5), the principal cGMP-catalyzing enzyme in the penis and the primary target of sildenafil (Viagra). We have isolated a 3.7-kb DNA fragment that contains the human PDE5A gene promoter. The DNA fragment contains a sequence of 234 nucleotides at its 3' end that corresponds to most of the untranslated region of the PDE5A1 mRNA. The remaining 3.5-kb upstream flanking sequence contains no apparent TATA box but has several sequences that resemble binding sequences for transcription factors such as androgen receptor (AR), AP1, AP2, AP4, Sp1, MyoD, Myc, and CArG. In search of promoter activities, we used a luciferase reporter system to examine 10 DNA fragments that cover various regions of the 3.7-kb fragment. We found that a full basal promoter activity was confined to a 139-bp region that includes 78 bp of the PDE5A1-specific first exon. A lesser basal promoter activity was still detectable in a 94-bp fragment that contains the same 78-bp PDE5A1-specific exon plus 16 bp of upstream sequence. Either the 139-bp or the 94-bp promoter fragment responded minimally to cAMP or cGMP (2 mM) stimulation. Longer fragments that contain either a 308-bp 5' extension (from the 138-bp fragment) or a 156-bp 3' extension (all exon sequence) responded at higher levels to cAMP and cGMP stimulation. The 5' and 3' extensions cooperated with each other to provide the highest level of responses to cAMP and cGMP stimulation. DNase I footprint analysis identified four AP2- and two Sp1-binding sites in the 5' extension and four Sp1-binding sites in the 3' extensions. Cyclic AMP and cGMP had similar stimulatory effects on the PDE5A promoter.
PDE5A基因编码5型磷酸二酯酶(PDE5),它是阴茎中主要的催化环磷酸鸟苷(cGMP)的酶,也是西地那非(伟哥)的主要作用靶点。我们分离出了一个包含人PDE5A基因启动子的3.7kb DNA片段。该DNA片段在其3'端含有一段234个核苷酸的序列,对应于PDE5A1 mRNA的大部分非翻译区。其余3.5kb的上游侧翼序列没有明显的TATA盒,但有几个序列类似于雄激素受体(AR)、AP1、AP2、AP4、Sp1、肌细胞增强因子2(MyoD)、原癌基因(Myc)和血清反应元件(CArG)等转录因子的结合序列。为了寻找启动子活性,我们使用荧光素酶报告系统检测了覆盖3.7kb片段各个区域的10个DNA片段。我们发现完整的基础启动子活性局限于一个139bp的区域,该区域包括PDE5A1特异性第一外显子的78bp。在一个94bp的片段中仍可检测到较低的基础启动子活性,该片段包含相同的78bp PDE5A1特异性外显子加上16bp的上游序列。139bp或94bp的启动子片段对环磷酸腺苷(cAMP)或cGMP(2mM)刺激的反应最小。包含308bp 5'延伸(来自138bp片段)或156bp 3'延伸(所有外显子序列)的较长片段对cAMP和cGMP刺激的反应水平更高。5'和3'延伸相互协作,对cAMP和cGMP刺激提供最高水平的反应。DNA酶I足迹分析在5'延伸中鉴定出四个AP2结合位点和两个Sp1结合位点,在3'延伸中鉴定出四个Sp1结合位点。环磷酸腺苷和环磷酸鸟苷对PDE5A启动子具有相似的刺激作用。