McGowan M H, Neubauer J A, Stolle C A
National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Gene. 1997 Feb 28;186(2):181-8. doi: 10.1016/s0378-1119(96)00700-7.
The rat carbonic anhydrase II gene was characterized and found to be approximately 15.5 kb in length and to contain 7 exons and 6 introns. All intron/exon junction and branch point sequences conform to consensus sequences, and the overall rat CA II genomic structure appears to be conserved upon comparison with mouse, human, and chicken CA II genes. The putative cis-acting elements within the analyzed 1014 bp 5' flanking region include: TATA box, 4 Sp1 binding sites, 2 AP2 sites and putative tissue-specific beta-globin-like repeat elements. A CpG island of approximately 800 bp was identified that begins about 600 bp upstream of exon 1 and extends about 200 bp into intron 1. In the 3' UTR, two polyadenylation signals (AATAAA) are present, the second of which is believed to be utilized. Northern blot analysis reveals that the 1.7 kb rat CA II mRNA is abundantly expressed in adult male brain and kidney, while negligible amounts are detected in heart and liver.
大鼠碳酸酐酶II基因经鉴定,发现其长度约为15.5 kb,包含7个外显子和6个内含子。所有内含子/外显子连接序列和分支点序列均符合共有序列,与小鼠、人类和鸡的碳酸酐酶II基因相比,大鼠碳酸酐酶II的整体基因组结构似乎是保守的。在所分析的1014 bp 5'侧翼区域内的假定顺式作用元件包括:TATA盒、4个Sp1结合位点、2个AP2位点以及假定的组织特异性β-珠蛋白样重复元件。鉴定出一个约800 bp的CpG岛,其起始于外显子1上游约600 bp处,并延伸至内含子1中约200 bp处。在3'非翻译区,存在两个聚腺苷酸化信号(AATAAA),据信使用的是第二个信号。Northern印迹分析显示,1.7 kb的大鼠碳酸酐酶II mRNA在成年雄性大鼠的脑和肾中大量表达,而在心脏和肝脏中检测到的量可忽略不计。