Vollrath D, Nathans J, Davis R W
Department of Biochemistry, Stanford University School of Medicine, CA 94305.
Science. 1988 Jun 17;240(4859):1669-72. doi: 10.1126/science.2837827.
Unequal crossing-over within a head-to-tail tandem array of the homologous red and green visual pigment genes has been proposed to explain the observed variation in green-pigment gene number among individuals and the prevalence of red-green fusion genes among color-blind subjects. This model was tested by probing the structure of the red and green pigment loci with long-range physical mapping techniques. The loci were found to constitute a gene array with an approximately 39-kilobase repeat length. The position of the red pigment gene at the 5' edge of the array explains its lack of variation in copy number. Restriction maps of the array in four individuals who differ in gene number are consistent with a head-to-tail configuration of the genes. These results provide physical evidence in support of the model and help to explain the high incidence of color blindness in the human population.
有人提出,同源的红色和绿色视觉色素基因的头对头串联阵列内的不等交换,可解释个体间观察到的绿色色素基因数量变化以及色盲受试者中红绿融合基因的普遍存在。通过使用长程物理图谱技术探测红色和绿色色素基因座的结构,对该模型进行了测试。发现这些基因座构成了一个重复长度约为39千碱基的基因阵列。红色色素基因在阵列5'边缘的位置解释了其拷贝数缺乏变化的原因。在基因数量不同的四个人中,该阵列的限制性图谱与基因的头对头排列一致。这些结果提供了支持该模型的物理证据,并有助于解释人群中色盲的高发病率。