Reyniers E, Van Thienen M N, Meire F, De Boulle K, Devries K, Kestelijn P, Willems P J
Department of Medical Genetics, University of Antwerp, Belgium.
Genomics. 1995 Sep 20;29(2):323-8. doi: 10.1006/geno.1995.9998.
Blue cone monochromacy is an X-linked condition in which the function of both the red pigment gene (RCP) and the green pigment gene (GCP) is impaired. Blue cone monochromacy can be due to a red/green gene array rearrangement existing of a single red/green hybrid gene and an inactivating C203R point mutation in GCP. We describe here a family with blue cone monochromacy due to the presence of the C203R mutation in both RCP and GCP. The flanking sequences of the C203R mutation in exon 4 of RCP were characteristic for GCP, indicating that this mutation was transferred from GCP into RCP by gene conversion.
蓝色视锥细胞单色症是一种X连锁疾病,其中红色色素基因(RCP)和绿色色素基因(GCP)的功能均受损。蓝色视锥细胞单色症可能是由于存在由单个红/绿杂交基因和GCP中一个失活的C203R点突变组成的红/绿基因阵列重排。我们在此描述一个因RCP和GCP中均存在C203R突变而患有蓝色视锥细胞单色症的家族。RCP第4外显子中C203R突变的侧翼序列具有GCP的特征,表明该突变是通过基因转换从GCP转移到RCP的。