Costanzi Egidia, Beccari Tommaso, Aisa Maria Cristina, Tiribuzi Roberto, Hopwood John J, Orlacchio Aldo
Dipartimento di Scienze Biochimiche e Biotecnologie Molecolari, Università degli Studi di Perugia, Via del Giochetto, 06012, Perugia, Italy.
Gene. 2003 May 22;310:143-9. doi: 10.1016/s0378-1119(03)00531-6.
Sulphamidase is a lysosomal enzyme necessary for the degradation of heparan sulphate. The deficiency of this hydrolase causes a disorder known as mucopolysaccharidosis type IIIA, characterized by a profound neurological deterioration. Human and mouse exon-intron structures were reported without any characterization of their promoter regions [DNA Res. 3 (1996) 269; Mamm. Genome 11 (2000) 436]. The promoter region was isolated and characterized to understand the factors affecting the expression of mouse sulphamidase. The 5'-flanking region was shown to contain a GC-rich region and putative binding sites for the transcription factors SRY, MZF1 and Nkx-2.5 with no TATA or CAAT boxes present. The 5' region had promoter activity to drive luciferase gene expression in transfected COS cells. The transcription initiation site of mouse sulphamidase was mapped to a single adenine residue 355 bases upstream of ATG codon. Northern blot analysis revealed differential expression of a major transcript of 4.5 kb in all tissues examined. Finally, the 3'-untranslated region of the mouse sulphamidase gene was isolated and found to be longer than the region identified in the human gene.
硫酸酰胺酶是一种降解硫酸乙酰肝素所必需的溶酶体酶。这种水解酶的缺乏会导致一种名为IIIA型黏多糖贮积症的疾病,其特征是严重的神经功能恶化。已报道了人和小鼠的外显子-内含子结构,但未对其启动子区域进行任何表征[《DNA研究》3 (1996) 269;《哺乳动物基因组》11 (2000) 436]。为了解影响小鼠硫酸酰胺酶表达的因素,对其启动子区域进行了分离和表征。结果表明,5'侧翼区域含有一个富含GC的区域以及转录因子SRY、MZF1和Nkx-2.5的假定结合位点,不存在TATA盒或CAAT盒。该5'区域具有启动子活性,可在转染的COS细胞中驱动荧光素酶基因表达。小鼠硫酸酰胺酶的转录起始位点被定位到ATG密码子上游355个碱基处的一个腺嘌呤残基。Northern印迹分析显示,在所检测的所有组织中,4.5 kb的主要转录本存在差异表达。最后,分离出了小鼠硫酸酰胺酶基因的3'非翻译区,发现其比人类基因中鉴定出的区域更长。