Molecular cloning, genomic characterization and expression of novel human alpha1A-adrenoceptor isoforms.
Chang DJ,
Chang TK,
Yamanishi SS,
Salazar FH,
Kosaka AH,
Khare R,
Bhakta S,
Jasper JR,
Shieh IS,
Lesnick JD,
Ford AP,
Daniels DV,
Eglen RM,
Clarke DE,
Bach C,
Chan HW.
Center for Biological Research, Neurobiology Unit, Roche Bioscience, Palo Alto, CA 94304, USA. david-j.chang@roche.com
We have isolated and characterized from human prostate novel splice variants of the human alpha1A-adrenoceptor, several of which generate truncated products and one isoform, alpha(1A-4), which has the identical splice site as the three previously described isoforms. Long-PCR on human genomic DNA showed that the alpha(1A-4) exon is located between those encoding the alpha(1A-1) and alpha(1A-3) variants. CHO-K1 cells stably expressing alpha(1A-4) showed ligand binding properties similar to those of the other functional isoforms as well as agonist-stimulated inositol phosphate accumulation. Quantitative PCR analyses revealed that alpha(1A-4) is the most abundant isoform expressed in the prostate with high levels also detected in liver and heart.
PMID: 9490024 [PubMed - indexed for MEDLINE]