CHROMOSOMAL LOCALIZATION AND GENOMIC ORGANIZATION OF GENES ENCODING GUANYLYL CYCLASE RECEPTORS EXPRESSED IN OLFACTORY SENSORY NEURONS AND RETINA

Citation
Rb. Yang et al., CHROMOSOMAL LOCALIZATION AND GENOMIC ORGANIZATION OF GENES ENCODING GUANYLYL CYCLASE RECEPTORS EXPRESSED IN OLFACTORY SENSORY NEURONS AND RETINA, Genomics, 31(3), 1996, pp. 367-372
Citations number
39
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
08887543
Volume
31
Issue
3
Year of publication
1996
Pages
367 - 372
Database
ISI
SICI code
0888-7543(1996)31:3<367:CLAGOO>2.0.ZU;2-D
Abstract
We recently cloned three membrane guanylyl cyclases, designated GC-D, GC-E, and GC-F, from rat olfactory tissue and eye. Amino acid sequence homology suggests that they may compose a new gene subfamily of guany lyl cyclase receptors specifically expressed in sensory tissues. Their chromosomal localization was determined by mouse interspecific backcr oss analysis. The GC-D, GC-E, and GC-F genes (Gucy2d, Gucy2e, and Gucy 2f) are dispersed through the mouse genome in that they map to chromos omes 7, 11, and X, respectively. Close proximity of the mouse GC-D gen e to Omp (olfactory marker protein) and Hbb (hemoglobin beta-chain com plex) suggests that the human homolog gene maps to 11p15.4 or 11q13.4- q14.1. The human GC-F gene was localized to the long arm of chromosome Xq22 by fluorescence in situ hybridization. The genomic organization of the mouse GC-E gene was determined and compared to other guanylyl c yclase genes. The mouse GC-D, GC-E, and GC-F genomic clones contain id entical exon-intron boundaries within their extracellular and cytoplas mic domains, demonstrating the conservation of the gene structures. Wi th respect to human genetic diseases, GC-E mapped to mouse chromosome 11 within a syntenic region on human chromosome 17p13 that has been li nked with loci for autosomal dominant retinitis pigmentosa and Leber c ongenital amaurosis. No apparent disease loci have been yet linked to the locations of the GC-D or GC-F genes. (C) 1996 Academic Press, Inc.