Scragg I, Celier C, Burchell B
FEBS Lett. 1985 Apr 8;183(1):37-42. doi: 10.1016/0014-5793(85)80949-2.
Three major UDP-glucuronyltransferase isoenzymes (50-54 kDa) have been identified by immunoblot analysis. Bilirubin UDP-glucuronyltransferase (54 kDa) was specially induced by treatment of the rats with clofibrate. This isoenzyme was not detectable in liver microsomal extracts from congenitally jaundiced Gunn rats and was not induced by treatment of these animals with clofibrate. Phenol UDP-glucuronyltransferase, the only isoenzyme determined to be present in foetal Wistar rat liver microsomes was not detected by enzyme assay or immunoblot analysis of foetal Gunn rat liver microsomal extracts. These results provide the first indication that bilirubin UDP-glucuronyltransferase and possible phenol UDP-glucuronyltransferase proteins are not present in the congenitally jaundiced Gunn rat.
通过免疫印迹分析已鉴定出三种主要的UDP-葡萄糖醛酸基转移酶同工酶(50 - 54 kDa)。胆红素UDP-葡萄糖醛酸基转移酶(54 kDa)经氯贝丁酯处理大鼠后被特异性诱导。在先天性黄疸的冈恩大鼠的肝微粒体提取物中未检测到这种同工酶,并且用氯贝丁酯处理这些动物后也不会诱导其产生。苯酚UDP-葡萄糖醛酸基转移酶是唯一在胎儿Wistar大鼠肝微粒体中检测到的同工酶,但通过酶测定或对胎儿冈恩大鼠肝微粒体提取物的免疫印迹分析均未检测到。这些结果首次表明先天性黄疸的冈恩大鼠中不存在胆红素UDP-葡萄糖醛酸基转移酶以及可能的苯酚UDP-葡萄糖醛酸基转移酶蛋白。