Pfister K, Chapman V, Watson G, Paigen K
J Biol Chem. 1985 Sep 25;260(21):11588-94.
Two new haplotypes of the [Gus] gene complex have been characterized following their transfer from Mus musculus castaneus, where they were found, to a C57BL/6J genetic background. The [GUS]CS haplotype carries a new structural allele, Gus-scs, coding for enzyme with decreased thermolability and lacking an antigenic site present in other beta-glucuronidase allozymes. The [Gus]CL haplotype carries another new structural allele, Gus-scl, that codes for enzyme with increased thermolability and possessing the antigenic site. Both CS and CL beta-glucuronidase have the same catalytic activity/molecule as the standard B allozyme from C57BL/6J mice. Mice carrying either the [Gus]CS or [Gus]CL haplotype have reduced enzyme activity in all tissues examined at all stages of development. The reduced enzyme activity is partially accounted for by reduced rates of enzyme synthesis, and the remainder probably results from increased rates of enzyme turnover. beta-Glucuronidase mRNA levels in these mice were not reduced suggesting that the observed reduction in enzyme synthesis is due to a decreased efficiency of translation for CS and CL mRNA.
在将[Gus]基因复合体从发现它们的小家鼠栗色亚种转移到C57BL/6J遗传背景后,已对两种新的单倍型进行了表征。[GUS]CS单倍型携带一个新的结构等位基因Gus-scs,它编码的酶热稳定性降低,并且缺乏其他β-葡萄糖醛酸酶同工酶中存在的一个抗原位点。[Gus]CL单倍型携带另一个新的结构等位基因Gus-scl,它编码的酶热稳定性增加且具有该抗原位点。CS和CLβ-葡萄糖醛酸酶与来自C57BL/6J小鼠的标准B同工酶具有相同的催化活性/分子。携带[Gus]CS或[Gus]CL单倍型的小鼠在发育的所有阶段,在所检查的所有组织中酶活性均降低。酶活性降低部分是由于酶合成速率降低,其余可能是由于酶周转速率增加。这些小鼠中的β-葡萄糖醛酸酶mRNA水平未降低,这表明观察到的酶合成减少是由于CS和CL mRNA的翻译效率降低所致。