Suppr超能文献

大鼠碳酸酐酶II基因结构的表征:5'侧翼区和3'非翻译区的序列分析

Characterization of the rat carbonic anhydrase II gene structure: sequence analysis of the 5' flanking region and 3' UTR.

作者信息

McGowan M H, Neubauer J A, Stolle C A

机构信息

National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Gene. 1997 Feb 28;186(2):181-8. doi: 10.1016/s0378-1119(96)00700-7.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验