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The molecular basis of the inherited deficiency of androsterone UDP‐glucuronyltransferase in Wistar rats

机译:Wistar大鼠雄性激素UDP-葡萄糖醛酸转移酶遗传缺陷的分子基础

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>A major UDP-glucurnoyltransferase isoenzyme in rat liver (51 kDa), corresponding to androsterone glucuronidating activity, has been identified by immunoblot analysis. This isoenzyme is absent from Wistar rats exhibiting the low androsterone (LA) UDP-glucuronyltransferase activity phenotype. Northern blot analysis of total RNA from normal and androsterone glucuronidation deficient Wistar rats demonstrated that the mRNA encoding this protein was not synthesised. Differences in restriction fragment length observed on Southern blotting of genomic DNA from LA Wistar rats indicate that this inherited deficiency is the result of a deletion in the androsterone UDP-glucuronyltransferase gene.
机译:通过免疫印迹分析已鉴定出大鼠肝脏中的主要UDP-葡萄糖醛酸转移酶同工酶(51 kDa),与雄甾酮葡萄糖醛酸化活性相对应。 Wistar大鼠缺少这种同工酶,表现出低的雄甾酮(LA)UDP-葡萄糖醛酸转移酶活性表型。来自正常和雄甾酮葡萄糖醛酸缺乏症Wistar大鼠的总RNA的RNA印迹分析表明,编码该蛋白的mRNA没有合成。在对来自LA Wistar大鼠的基因组DNA的Southern印迹中观察到的限制性片段长度的差异表明,这种遗传缺陷是雄甾酮UDP-葡萄糖醛酸转移酶基因缺失的结果。

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