Inase N, Fushimi K, Ishibashi K, Uchida S, Ichioka M, Sasaki S, Marumo F
Second Department of Internal Medicine, Tokyo Medical and Dental University, Japan.
J Biol Chem. 1995 Jul 28;270(30):17913-6. doi: 10.1074/jbc.270.30.17913.
Human aquaporin 3 (AQP3) gene was isolated, and its structural organization was characterized. The gene appeared to exist as a single copy in the human genome and to comprise six exons distributing over 7 kilobases. The sizes of the exons are 171, 127, 138, 119, 218, and 1035 base pairs, and those of introns are approximately 3530, 300, 350, 330, and 90 base pairs, respectively. The initiation site of transcription was identified to locate 64 base pairs upstream of the first ATG codon by primer extension analysis and ribonuclease protection assay. The 5'-flanking region has a TATA box, two Sp1 sequences, and some consensus sequences including AP2 sites. With luciferase assay, the 5'-flanking region was demonstrated to have a promoter activity, which is up-regulated 4-fold by phorbol ester. These findings about the genomic clone of human AQP3 will contribute to elucidate the molecular mechanism of transcriptional regulation of AQP3.
人类水通道蛋白3(AQP3)基因被分离出来,并对其结构组织进行了表征。该基因在人类基因组中似乎以单拷贝形式存在,由分布在7千碱基上的六个外显子组成。外显子的大小分别为171、127、138、119、218和1035个碱基对,内含子的大小分别约为3530、300、350、330和90个碱基对。通过引物延伸分析和核糖核酸酶保护试验确定转录起始位点位于第一个ATG密码子上游64个碱基对处。5'侧翼区域有一个TATA盒、两个Sp1序列以及一些包括AP2位点在内的共有序列。通过荧光素酶测定,证明5'侧翼区域具有启动子活性,佛波酯可使其上调4倍。关于人类AQP3基因组克隆的这些发现将有助于阐明AQP3转录调控的分子机制。