Watson G, Jaussi R, Tabron D, Paigen K
Jackson Laboratory, Bar Harbor, Maine 04609.
Biochem Genet. 1993 Apr;31(3-4):155-66. doi: 10.1007/BF02399922.
Both enzyme activity and mRNA concentration of beta-glucuronidase were measured in kidneys of mice treated with testosterone and the synthetic estrogen, diethylstilbestrol. Six congenic strains, all having a C57BL6/J genetic background but each having a different haplotype of the beta-glucuronidase gene complex, were compared. In each strain the induction caused by androgen was partially repressed by estrogen. The extent of this antagonism varied among the six haplotypes and was not coordinate with the extent of induction by androgen alone. Antagonism appears to be regulated by at least two alleles of a new locus, Gus-e, within the beta-glucuronidase gene complex. Repression by estrogen, like induction by androgen, appears to take place primarily at the transcriptional level. Kinetic studies revealed that estrogen causes the androgen response curve to plateau earlier and at a lower level. This suggests that estrogen increases the rate of gene deactivation rather than decreasing the rate of gene activation. Isoelectric focusing of beta-glucuronidase from Gus-ea and Gus-eb mice and their F1 progeny revealed that the genes are regulated in cis. Together, these findings support a model in which both sex hormones exert their effects on separate DNA response elements located in close proximity to the gene or within the gene itself.
在接受睾酮和合成雌激素己烯雌酚处理的小鼠肾脏中,测量了β-葡萄糖醛酸酶的酶活性和mRNA浓度。比较了六个同源近交系,它们均具有C57BL6/J遗传背景,但每个品系的β-葡萄糖醛酸酶基因复合体具有不同的单倍型。在每个品系中,雄激素引起的诱导作用都被雌激素部分抑制。这种拮抗作用的程度在六种单倍型中各不相同,并且与单独雄激素诱导的程度不相关。拮抗作用似乎受β-葡萄糖醛酸酶基因复合体内一个新位点Gus-e的至少两个等位基因调控。与雄激素诱导一样,雌激素的抑制作用似乎主要发生在转录水平。动力学研究表明,雌激素使雄激素反应曲线更早且在更低水平达到平稳。这表明雌激素增加了基因失活的速率,而不是降低了基因激活的速率。对来自Gus-ea和Gus-eb小鼠及其F1后代的β-葡萄糖醛酸酶进行等电聚焦分析,结果显示这些基因是顺式调控的。这些发现共同支持了一个模型,即两种性激素都对位于基因附近或基因本身内的不同DNA反应元件发挥作用。