Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11

• Published in: Genomics (San Diego, Calif.) Vol. 51; no. 3; pp. 325 - 331
• Main Authors: Wissinger, Bernd, Jägle, Herbert, Kohl, Susanne, Broghammer, Martina, Baumann, Britta, Hanna, David B, Hedels, Christian, Apfelstedt-Sylla, Eckhard, Randazzo, Giorgio, Jacobson, Samuel G, Zrenner, Eberhart, Sharpe, Lindsay T
• Format: Journal Article
• Language: English
• Published: San Diego, CA Elsevier Inc 01.08.1998; Elsevier
• Subjects: Biological and medical sciences; Chromosome Breakage - genetics; Chromosome Mapping; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 2 - genetics; Cloning, Molecular; Color Vision Defects - genetics; Cyclic Nucleotide-Gated Cation Channels; Genes, Recessive; Genetic Linkage - genetics; Homozygote; Humans; Ion Channels - genetics; Ion Channels - physiology; Lod Score; Medical sciences; Meiosis - genetics; Microsatellite Repeats - genetics; Ophthalmology; Pedigree; Retinal Cone Photoreceptor Cells - physiopathology; Retinal Rod Photoreceptor Cells - physiopathology; Vision disorders; Genetic mapping; Human; Rod monochromatism; Cone; Linkage; Vision disorder; Rod; Photoreceptor; Critical region; Chromosome A2; Retina; Genetic disease; Eye disease; Gene; Dyschromatopsia; Physical map
• ISSN: 0888-7543; 1089-8646
• DOI: 10.1006/geno.1998.5390

We have performed linkage analysis in eight families with rod monochromacy, an autosomal recessively inherited condition with complete color blindness. Significant linkage was found with markers located at the pericentromeric region of chromosome 2. A maximum lod score of 5.36 was obtained for marker D2S2333 at θ = 0.00. Mapping of meiotic breakpoints localized the disease gene between markers D2S2187 and D2S2229. Homozygosity for a number of subsequent markers indicating identity by descent was found in two families and provides evidence for a further refinement of the locus proximal to D2S373. This defines an interval of ≈3 cM covering theACHM2locus for rod monochromacy. Radiation hybrid mapping of theCNGA3gene encoding the α-subunit of the cGMP gated cation channel in human cone photoreceptors resulted in a maximum lod score of 16.1 with marker D2S2311 combined with a calculated physical distance of 6.19cR10,000. Screening of the CEPH YAC library and subsequent STS mapping indicated the physical order cen–D2S2222–D2S2175–(D2S2187/D2S2311)–qtel ofmarkers on 2q11 and showed that theCNGA3gene maps most closely to D2S2187 and D2S2311. These data indicate that theCNGA3gene maps within the critical interval of theACHM2locus for rod monochromacy and thus is a candidate gene for this disease.