1. ¹Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Seta, Otsu 520-2192, Japan
2. ²Institute of Vision Research, 12-23 Sanbonmatsu-cho, Atsuta-ku, Nagoya 456-0032, Japan
3. ³Department of Ophthalmology, Shiga University of Medical Science, Seta, Otsu 520-2192, Japan

Correspondence: Hisao Ueyama, Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Seta, Otsu 520-2192, Japan. E-mail: datt@belle.shiga-med.ac.jp

Received 5 March 2006; Accepted 2 May 2006; Published online 28 July 2006.

Abstract

Normal visual pigment gene arrays on the human X chromosome have a red gene at the first and a green gene at the second positions. More than half of the arrays have additional green genes downstream, but only the first two genes of the array are likely to be expressed in the retina. An array consisting of four genes in two Japanese participants, A121 and A447, was detected either by pulsed field gel electrophoresis and subsequent Southern hybridization or by single nucleotide primer extension reaction. In both participants, the first gene of the array was green, downstream genes were red and green, and the fourth gene was green. The red gene was determined to be at the second position by comparison of polymorphic sites among the intergenic regions that had been amplified by long-range PCR. Such an array with a reverse normal order of pigment genes, green-red as the first two, has never been reported before. They were expected to have normal color vision but showed protan deficiency (protanomaly), a phenotype lacking the red pigment. The red gene had no mutations in the exons and exon/intron boundaries, but had an A-71C substitution in the promoter in both participants.