Schofield A E, Martin P G, Spillett D, Tanner M J
Department of Biochemistry, School of Medical Sciences, University of Bristol, UK.
Blood. 1994 Sep 15;84(6):2000-12.
The structure and sequence of the human red blood cell anion exchanger (EPB3, AE1, band 3) gene was determined by analysis of genomic and cDNA clones. The gene extends over 18 kb and consists of 20 exons. The cDNA sequence comprises 4,906 nucleotides [excluding the poly(A) tail]. There is extensive similarity between the human and mouse AE1 gene, although the latter covers 17 kb. The additional sequence present within the human AE1 gene compared with the mouse gene is mainly caused by the presence of 6 Alu repetitive units in the human gene between intron 13 and exon 20, one of which is within the 3' noncoding region of the cDNA. Two potential promoter regions within the human AE1 gene are located so that they could give rise to the different transcripts found in erythroid cells and in the kidney. The kidney transcript would lack exons 1 through 3 of the erythroid transcript. The translation initiator downstream to the human kidney promoter would give rise to a protein with a 20 amino acid section at the N-terminus that is not present in the erythroid human AE1 protein or the rodent kidney AE1 proteins.
通过对基因组和cDNA克隆进行分析,确定了人类红细胞阴离子交换蛋白(EPB3、AE1、带3蛋白)基因的结构和序列。该基因跨度超过18kb,由20个外显子组成。cDNA序列包含4906个核苷酸[不包括聚腺苷酸尾]。人类和小鼠的AE1基因之间存在广泛的相似性,尽管后者覆盖17kb。与小鼠基因相比,人类AE1基因中存在的额外序列主要是由于人类基因在内含子13和外显子20之间存在6个Alu重复单元,其中一个位于cDNA的3'非编码区内。人类AE1基因内的两个潜在启动子区域的位置,使得它们可能产生在红细胞和肾脏中发现的不同转录本。肾脏转录本将缺少红细胞转录本的外显子1至3。人类肾脏启动子下游的翻译起始位点将产生一种在N端有20个氨基酸片段的蛋白质,该片段在人类红细胞AE1蛋白或啮齿动物肾脏AE1蛋白中不存在。