Timms G P, Holmes R S
Biochem Genet. 1981 Dec;19(11-12):1223-36. doi: 10.1007/BF00484575.
Variation in the inducibility of the liver microsomal isozyme of aldehyde dehydrogenase (designated AHD-Cy) by phenobarbital administration was observed among inbred strains an linkage testing stocks of Mus musculus. The phenotypes were inherited in a normal Mendelian fashion with two alleles showing codominance at a proposed regulatory locus (designated Ahd-3r). Strain variation was also observed for the induction of liver AHD-Cy by 17 -Beta-oestradiol administration to ovarectimized female mice. Moreover, this enzyme was elevated in activity by the administration of high (nonphysiological) levels of progesterone. Development studies showed that the liver and kidney AHD-Cy isozyme exhibited low activities in late-stage fetal and neonatal mice and reached adult levels by approximately 6 weeks of age.
在小家鼠的近交系和连锁测试群体中,观察到通过给予苯巴比妥诱导肝脏微粒体醛脱氢酶同工酶(称为AHD-Cy)的能力存在差异。这些表型以正常孟德尔方式遗传,两个等位基因在一个假定的调控位点(称为Ahd-3r)表现为共显性。对卵巢切除的雌性小鼠给予17-β-雌二醇后,肝脏AHD-Cy的诱导也存在品系差异。此外,给予高(非生理)水平的孕酮会使该酶的活性升高。发育研究表明,肝脏和肾脏的AHD-Cy同工酶在晚期胎儿和新生小鼠中活性较低,大约在6周龄时达到成年水平。