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 |
(c)American Society for Biochemistry and Molecular Biology (ASBMB) |
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 |