TY - JOUR
T1 - Genomic organisation and chromosomal localisation of the gene encoding human beta adducin
AU - Tisminetzky, Sergio
AU - Devescovi, Giulia
AU - Tripodi, Grazia
AU - Muro, Andres
AU - Bianchi, Giuseppe
AU - Colombi, Marina
AU - Moro, Laura
AU - Barlati, Sergio
AU - Tuteja, Renu
AU - Baralle, Francisco E.
PY - 1995/12/29
Y1 - 1995/12/29
N2 - 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.
AB - 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.
KW - Alternative splicing
KW - chromosome 2
KW - cytoskeletal protein
KW - exon-intron organisation
KW - genomic library
KW - in situ hybridisation
UR - http://www.scopus.com/inward/record.url?scp=0029617975&partnerID=8YFLogxK
U2 - 10.1016/0378-1119(95)00591-9
DO - 10.1016/0378-1119(95)00591-9
M3 - Article
SN - 0378-1119
VL - 167
SP - 313
EP - 316
JO - Gene
JF - Gene
IS - 1-2
ER -