Seth P, Leibach F H, Ganapathy V
Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta 30912-2100, USA.
Biochem Biophys Res Commun. 1997 Dec 18;241(2):535-40. doi: 10.1006/bbrc.1997.7840.
We have isolated a mouse cDNA which codes for a functional type 1 sigma receptor. The functional identity of the cDNA was established by expressing the cDNA in mammalian cells and measuring the cDNA-induced binding of haloperidol. Using this cDNA as the probe, we have isolated a murine genomic clone which contains the type 1 sigma receptor gene in its entirety. We have sequenced the gene completely, deduced the exon-intron organization and analyzed the promoter region sequence for transcription factor binding sites. The gene (approximately 7 kbp) is TATA-less but contains CCAATC and GC boxes immediately upstream of the transcription start site. The gene consists of 4 exons and 3 introns. The 5'-flanking region contains putative binding sites for AP-1, AP-2, GATA-1 and steroid receptors.
我们分离出了一个编码功能性1型西格玛受体的小鼠cDNA。通过在哺乳动物细胞中表达该cDNA并测量其诱导的氟哌啶醇结合,确定了该cDNA的功能特性。以这个cDNA为探针,我们分离出了一个完整包含1型西格玛受体基因的小鼠基因组克隆。我们对该基因进行了完全测序,推导了外显子-内含子结构,并分析了启动子区域序列中的转录因子结合位点。该基因(约7kbp)没有TATA盒,但在转录起始位点上游紧邻处含有CCAATC和GC盒。该基因由4个外显子和3个内含子组成。5'侧翼区域含有AP-1、AP-2、GATA-1和类固醇受体的假定结合位点。