Abstract
Adducin (ADD) is a heterodimeric protein of the membrane skeleton with subunits of 103 (α) and 97 kDa (β). It promotes the assembly of the spectrin-actin network. We have previously shown that one point mutation in each of the α and β rat ADD-encoding genes is associated with blood pressure variation in an animal model for hypertension, the Milan hypertensive strain of rats, probably due to a change in the phosphorylation pattern. In fact, the rat mutations, Y to F for α and R to Q for β, are located, respectively, in a tyrosine kinase and a protein kinase A phosphorylation site. We have now determined, for the human β-ADD-encoding gene, its chromosomal localisation, exon-intron organisation and alternative splicing patterns. We report here that human β-ADD is localised on chromosome 2 and we also show a characteristic 3′ end alternative splicing of the β-ADD RNA that generates two distinct β-ADD families, namely ADD 63 and 97; both of them in turn present a very complex differential splicing pattern in the internal exons.
| Original language | English |
|---|---|
| Pages (from-to) | 313-316 |
| Number of pages | 4 |
| Journal | Gene |
| Volume | 167 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 29 Dec 1995 |
| Externally published | Yes |
Keywords
- Alternative splicing
- chromosome 2
- cytoskeletal protein
- exon-intron organisation
- genomic library
- in situ hybridisation
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