Wirkner U, Voss H, Ansorge W, Pyerin W
Deutsches Krebsforschungszentrum, Heidelberg, Germany.
Genomics. 1998 Feb 15;48(1):71-8. doi: 10.1006/geno.1997.5136.
The isolation and characterization of the complete gene coding for human protein kinase CK2 catalytic subunit alpha is described. The gene spans 70 kb and consists of 13 exons, and the exon/intron boundaries conform to the gt/ag rule. Exons range in size from 51 to 2960 bp, introns from 527 to around 34000 bp. The translation start site is located in Exon 2, the stop codon in Exon 13. Two transcription start sites were identified by primer extension analysis: The further 5'-located site defines position 1 of the gene, the second site is located at position 50. The 5' region of the CK2 alpha gene shows features of a housekeeping promoter, such as lack of a TATA box and presence of a CpG island and GC boxes. The region was analyzed by reporter gene assay, and promoter activity was detected within the region ranging from position -256 to 144. Six potential polyadenylation signals were identified in the 3' noncoding region of the CK2 alpha gene. As indicated by comparison with expressed sequence tags from the EMBL databank and by Northern-blot analysis, the most 3' located, active polyadenylation signal seems to be the fourth signal, defining the end of the gene.
本文描述了编码人蛋白激酶CK2催化亚基α的完整基因的分离与特性。该基因跨度为70kb,由13个外显子组成,外显子/内含子边界符合gt/ag规则。外显子大小从51bp到2960bp不等,内含子从527bp到约34000bp。翻译起始位点位于外显子2中,终止密码子位于外显子13中。通过引物延伸分析确定了两个转录起始位点:位于5'端更远的位点定义为基因的第1位,第二个位点位于第50位。CK2α基因的5'区域显示出管家启动子的特征,如缺乏TATA盒、存在CpG岛和GC盒。通过报告基因检测对该区域进行了分析,在-256至144位的区域内检测到了启动子活性。在CK2α基因的3'非编码区域鉴定出六个潜在的聚腺苷酸化信号。与EMBL数据库中的表达序列标签比较以及Northern印迹分析表明,最靠近3'端的活性聚腺苷酸化信号似乎是第四个信号,它定义了基因的末端。