Brilliant M H, Gondo Y
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Pigment Cell Res. 1992 Nov;5(5 Pt 2):271-3. doi: 10.1111/j.1600-0749.1992.tb00548.x.
The mouse pink-eyed dilution locus, p, located on chromosome 7, mediates coat and eye color. The human correlate of this gene may underlie some forms of tyrosinase-positive oculocutaneous albinism. Mutations at the p locus result in a reduction in pigmentation of the eyes and coat. Although most mutant p alleles (including all spontaneous mutations) affect only pigmentation, several mutant alleles (all radiation induced) are also associated with a variety of other phenotypes. We have focused our attention on the p(un) mutant allele, a spontaneous mutation, exhibiting one of the highest reversion frequencies reported for a mammalian mutation. Using a new technique, genome scanning, we have cloned fragments of genomic DNA from the p locus that are associated with a DNA duplication in p(un) DNA. These fragments can now be used to locate the p gene-encoding sequences and aid in the molecular characterization of complex mutant p alleles.
小鼠的粉红眼稀释基因座p位于7号染色体上,介导被毛和眼睛的颜色。该基因在人类中的对应基因可能是某些类型的酪氨酸酶阳性眼皮肤白化病的基础。p基因座的突变会导致眼睛和被毛色素沉着减少。虽然大多数突变的p等位基因(包括所有自发突变)仅影响色素沉着,但有几个突变等位基因(均由辐射诱导)也与多种其他表型相关。我们将注意力集中在p(un)突变等位基因上,这是一种自发突变,表现出哺乳动物突变中报道的最高回复频率之一。使用一种新技术——基因组扫描,我们从p基因座克隆了与p(un) DNA中的DNA重复相关的基因组DNA片段。这些片段现在可用于定位p基因的编码序列,并有助于对复杂的突变p等位基因进行分子表征。