Hoefsloot L H, Hoogeveen-Westerveld M, Reuser A J, Oostra B A
MGC-Department of Cell Biology and Genetics, Erasmus University, Rotterdam, The Netherlands.
Biochem J. 1990 Dec 1;272(2):493-7. doi: 10.1042/bj2720493.
The gene coding for human lysosomal alpha-glucosidase was cloned and its structure was determined. The gene is approx. 20 kb long, and contains 20 exons. The first exon is non-coding. The coding sequence of the putative catalytic site domain is interrupted in the middle by an intron of 101 bp. This intron is not conserved in the highly similar region of the human and rabbit isomaltase genes. The promoter region was defined by a CAT assay and the start of the mRNA was determined by primer extension. The promoter has features characteristic of a 'housekeeping' gene. The GC content is high (80%) and distinct TATA and CCAAT motifs are lacking. Two potential binding sites for the AP-2 transcription factor are present. Four potential Sp-1 binding sites are located downstream of the 5' end of the mRNA.
编码人溶酶体α-葡萄糖苷酶的基因被克隆并确定了其结构。该基因长度约为20kb,包含20个外显子。第一个外显子是非编码的。假定催化位点结构域的编码序列在中间被一个101bp的内含子打断。该内含子在人和兔异麦芽糖酶基因的高度相似区域中不保守。通过CAT分析确定了启动子区域,并通过引物延伸确定了mRNA的起始位置。该启动子具有“管家”基因的特征。GC含量高(80%),缺乏明显的TATA和CCAAT基序。存在两个AP-2转录因子的潜在结合位点。四个潜在的Sp-1结合位点位于mRNA 5'端下游。