Takahashi Shigeru, Dohi Naoki, Takahashi Yuji, Miura Takashi
Laboratory of Environmental Molecular Physiology, School of Life Science, Tokyo University of Pharmacy and Life Science, 1432-1, Horinouchi, Hachioji, 192-0392, Tokyo, Japan.
Biochim Biophys Acta. 2002 Apr 12;1574(3):354-8. doi: 10.1016/s0167-4781(01)00360-8.
Prolyl 4-hydroxylase (P4H), an alpha(2)beta(2) tetramer, plays a crucial role in collagen synthesis. It catalyzes the hydroxylation of proline residues in X-Pro-Gly sequences to form 4-hydroxyproline. We isolated a genomic clone of the rat P4Halpha(I) gene. Approx. 0.6 kb of the fragment, which contained the 5'-flanking region, exon 1, and intron 1, was sequenced. Computer analysis revealed several motifs that may act as binding sites for basal transcription factors. To elucidate the regulation of the rat P4Halpha(I) gene expression, we assessed the 0.6 kb 5'-flanking region of the P4Halpha(I) gene for basal promoter activity. A series of deletion mutants of the 5'-flanking region linked to the luciferase gene was constructed. The basal expression level of these constructs was determined in fetal rat lung fibroblasts and Hepa-1 hepatoma cells. By measuring the luciferase activity, we found a positive-regulatory region at positions -246 to -165 bp.
脯氨酰4-羟化酶(P4H)是一种α(2)β(2)四聚体,在胶原蛋白合成中起关键作用。它催化X-Pro-Gly序列中脯氨酸残基的羟化反应,形成4-羟脯氨酸。我们分离出了大鼠P4Hα(I)基因的一个基因组克隆。对包含5'-侧翼区、外显子1和内含子1的约0.6 kb片段进行了测序。计算机分析揭示了几个可能作为基础转录因子结合位点的基序。为了阐明大鼠P4Hα(I)基因表达的调控机制,我们评估了P4Hα(I)基因0.6 kb的5'-侧翼区的基础启动子活性。构建了一系列与荧光素酶基因相连的5'-侧翼区缺失突变体。在胎鼠肺成纤维细胞和Hepa-1肝癌细胞中测定了这些构建体的基础表达水平。通过测量荧光素酶活性,我们在-246至-165 bp位置发现了一个正调控区域。