School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju, 500-712, Korea.
Mol Biol Rep. 2013 Feb;40(2):787-96. doi: 10.1007/s11033-012-2116-8. Epub 2012 Oct 12.
ADAM2, a member of the 'a disintegrin and metalloprotease' (ADAM) family, is a key protein in mammalian fertilization that is specifically expressed in testicular germ cells. Here, we investigated the transcriptional regulation of the mouse Adam2 gene. An in silico analysis identified two conserved non-coding sequences located upstream of the mouse and human ADAM2 genes. The upstream region of the mouse Adam2 gene was found to lack typical TATA and CAAT boxes, and to have a high GC content. Our in vitro transient transfection-reporter analysis identified a promoter in this region of the mouse Adam2 gene, along with regulatory regions that inhibit the activity of this promoter in somatic cells. Site-directed mutagenesis revealed that the caudal-type homeobox 1 and CCTC-binding factor motifs are responsible for the inhibitory activities of the repressor regions. Finally, electrophoretic mobility shift assays showed putative transcription factor-promoter DNA complexes, and DNA-affinity chromatography and proteomic analyses identified myelin gene regulatory factor as a binding partner of the Adam2 promoter. This provides the first identification and characterization of promoter and repressor regions that regulate the transcription of the mouse Adam2 gene, and offers insights into the regulation of this germ-cell-specific gene.
ADAM2 是“解整合素金属蛋白酶”(ADAM)家族的成员,是哺乳动物受精过程中的关键蛋白,特异性表达于睾丸生殖细胞。在这里,我们研究了小鼠 Adam2 基因的转录调控。计算机分析鉴定了位于小鼠和人 ADAM2 基因上游的两个保守非编码序列。发现小鼠 Adam2 基因的上游区域缺乏典型的 TATA 和 CAAT 盒,且 GC 含量较高。我们的体外瞬时转染报告分析鉴定了小鼠 Adam2 基因上游区域的启动子,以及在体细胞中抑制该启动子活性的调节区域。定点诱变揭示了尾型同源盒 1 和 CCTC 结合因子基序负责抑制区域的抑制活性。最后,电泳迁移率变动分析显示了假定的转录因子-启动子 DNA 复合物,DNA 亲和层析和蛋白质组学分析鉴定了髓鞘基因调控因子是 Adam2 启动子的结合伙伴。这首次鉴定和表征了调控小鼠 Adam2 基因转录的启动子和阻遏子区域,为研究这种生殖细胞特异性基因的调控提供了线索。