| First Author | Lecanda J | Year | 2000 |
| Journal | Biochem Biophys Res Commun | Volume | 276 |
| Issue | 1 | Pages | 117-24 |
| PubMed ID | 11006093 | Mgi Jnum | J:64830 |
| Mgi Id | MGI:1890024 | Doi | 10.1006/bbrc.2000.3439 |
| Citation | Lecanda J, et al. (2000) Molecular cloning and genomic organization of the mouse AE2 anion exchanger gene. Biochem Biophys Res Commun 276(1):117-24 |
| abstractText | The molecular organization of the AE2 (SLC4A2) gene, a member of the multigene family encoding sodium-independent chloride/bicarbonate anion exchangers, has previously been described in both humans and rats. In these two species, AE2 shows alternate promoter usages and tissue-specific expression of isoforms in a similar, but not identical, fashion. Here we report the molecular cloning and organization of the entire mouse AE2 gene. The gene consists of 23 exons and 22 introns and spans about 17 kb. Moreover, it drives transcription of N-terminal truncated isoforms from alternate promoter sequences in a way analogous to that described for rat and/or human orthologs. Thus, sequences within intron 2 function as overlapping alternate promoters for truncated isoforms AE2b(1) and AE2b(2), and sequences of intron 5 drive transcription of isoforms AE2c(1) and AE2c(2). Each of these variants has a specific alternative first exon, while remaining exons are common to the complete form of the message AE2a, the diversity at 5' leading to different N-termini in corresponding encoded proteins. As expected, mouse AE2 promoter sequences and the patterns of tissue expression of AE2 isoforms resemble rat counterparts more closely than human ones. Copyright 2000 Academic Press. |
