The structure and organization of the human erythroid anion exchanger (AE1) gene

• Published in: Genomics (San Diego, Calif.) Vol. 24; no. 3; p. 491
• Main Authors: Sahr, K E, Taylor, W M, Daniels, B P, Rubin, H L, Jarolim, P
• Format: Journal Article
• Language: English
• Published: United States 01-12-1994
• Subjects: Amino Acid Sequence; Animals; Anion Exchange Protein 1, Erythrocyte - genetics; Base Sequence; Biological Evolution; Chromosome Mapping; Cloning, Molecular; DNA Primers - genetics; DNA, Complementary - genetics; Erythrocytes - metabolism; Exons; Gene Library; Humans; Introns; Kidney - metabolism; Mice; Molecular Sequence Data; Promoter Regions, Genetic; Repetitive Sequences, Nucleic Acid; Sequence Homology, Nucleic Acid
• ISSN: 0888-7543
• DOI: 10.1006/geno.1994.1658

The AE1 (anion exchanger, band 3) protein is expressed in erythrocytes and in the A-type intercalated cells of the kidney distal collecting tubule. In both cell types it mediates the electroneutral transport of chloride and bicarbonate ions across the lipid bilayer, and, in erythrocytes, it also serves as the critical attachment site of the peripheral membrane skeleton. We have characterized the human AE1 gene using overlapping clones isolated from a phage library of human genomic DNA. The gene spans approximately 20 kb and consists of 20 exons separated by 19 introns. The structure of the human AE1 gene corresponds closely with that of the previously characterized mouse AE1 gene, with a high degree of conservation of exon/intron junctions, as well as exon and intron nucleotide sequences. The putative upstream and internal promoter sequences of the human AE1 gene used in erythroid and kidney cells, respectively, are described. We also report the nucleotide sequence of the entire 3' noncoding region of exon 20, which was lacking in the published cDNA sequences. In addition, we have characterized 9 Alu repeat elements found within the body of the human AE1 gene that are members of 4 related subfamilies that appear to have entered the genome at different times during primate evolution.