| Publication Type | journal article |
| School or College | School of Medicine |
| Department | Internal Medicine; Ophthalmology |
| Creator | Baehr, Wolfgang; Rao, Narayanam V. |
| Other Author | Haeseleer, F; Sokal, I; Li, N; Pettenati, M; Bronson, D; Wechter, R; Palczewski, K |
| Title | Molecular characterization of a third member of the guanylyl cyclase-activating protein subfamily |
| Date | 1999 |
| Description | The mammalian retina contains at least two guanylyl cyclases (GC1 and GC2) and two guanylyl cyclase-activating proteins (GCAP1 and GCAP2). Here we present evidence of the presence of a new photoreceptor-specific GCAP, termed GCAP3, which is closely related to GCAP1. The sequence similarity of GCAP3 with GCAP1 and GCAP2 is 57 and 49%, respectively. Recombinant GCAP3 and GCAP2 stimulate GC1 and GC2 in low [Ca2+]free and inhibit GCs when [Ca2+]free is elevated, unlike GCAP1, which only stimulates GC1. GCAP3 is encoded by a distinct gene present in other mammalian species but could not be detected by genomic Southern blotting in rodents, amphibians, and lower vertebrates. The intron/exon arrangement of the GCAP3 gene is identical to that of the other GCAP genes. While the GCAP1 and GCAP2 genes are arranged in a tail-to-tail array on chromosome 6p in human, the GCAP3 gene is located on 3q13.1, suggesting an ancestral gene duplication/translocation event. The identification of multiple Ca2+-binding proteins that interact with GC is suggestive of complex regulatory mechanisms for photoreceptor GC. |
| Type | Text |
| Publisher | American Society for Biochemistry and Molecular Biology (ASBMB) |
| Volume | 274 |
| Issue | 10 |
| First Page | 6526 |
| Last Page | 6535 |
| Subject | Amino Acid Sequence; Cloning, Molecular; Gene Expression Regulation |
| Subject MESH | Calcium-Binding Proteins; Guanylate Cyclase; Photoreceptors |
| Language | eng |
| Bibliographic Citation | Haeseleer F, Sokal I, Li N, Pettenati M, Rao N, Bronson D, Wechter R, Baehr W, Palczewski K. (1999). Molecular characterization of a third member of the guanylyl cyclase-activating protein subfamily. J Biol Chem, 274(10), 6526-35 |
| Rights Management | ©American Society for Biochemistry and Molecular Biology |
| Format Medium | application/pdf |
| Identifier | ir-main,1724 |
| ARK | ark:/87278/s6j10mvg |
| Setname | ir_uspace |
| ID | 707420 |
| Reference URL | https://collections.lib.utah.edu/ark:/87278/s6j10mvg |