Nagai F, Homma H, Tanase H, Matsui M
Kyoritsu College of Pharmacy, Tokyo, Japan.
Biochem J. 1988 Jun 15;252(3):897-900. doi: 10.1042/bj2520897.
Gunn rats, which have defects in bilirubin and 4-nitrophenol UDP-glucuronyltransferases (GT), were crossed with LA Wistar rats with a defect in androsterone GT. The F1 hybrids showed normal GT activities towards androsterone, bilirubin and 4-nitrophenol, demonstrating that Gunn and LA ('low activity') Wistar rats inherit a homozygous dominant trait for androsterone GT and bilirubin GT respectively. The F2 progeny showed four different combinations of bilirubin and androsterone GT activities: defects in both GT activities, a single defect in bilirubin GT activity, a single defect in androsterone GT activity and two normal GT activities. They were segregated in the approximate ratio of 1:3:3:9, which is compatible with Mendel's Principle of Independent Assortment. These results provide evidence that androsterone GT and bilirubin GT are located on different chromosomes. In the F2 generation, defective bilirubin and 4-nitrophenol GT activities were not segregated, indicating that these two mutant genes are closely linked on the same chromosome.
冈恩大鼠在胆红素和4-硝基苯酚UDP-葡萄糖醛酸基转移酶(GT)方面存在缺陷,将其与雄酮GT有缺陷的LA Wistar大鼠杂交。F1杂种对雄酮、胆红素和4-硝基苯酚表现出正常的GT活性,这表明冈恩大鼠和LA(“低活性”)Wistar大鼠分别继承了雄酮GT和胆红素GT的纯合显性性状。F2后代表现出胆红素和雄酮GT活性的四种不同组合:两种GT活性均有缺陷、胆红素GT活性单一缺陷、雄酮GT活性单一缺陷以及两种GT活性均正常。它们以近似1:3:3:9的比例分离,这与孟德尔独立分配定律相符。这些结果证明雄酮GT和胆红素GT位于不同的染色体上。在F2代中,有缺陷的胆红素和4-硝基苯酚GT活性没有分离,表明这两个突变基因在同一染色体上紧密连锁。