Kim S G, Kim Y H
Institute of Chemical Toxicology, Wayne State University, Detroit, Michigan 48201.
Mol Pharmacol. 1992 Jul;42(1):75-81.
Expression of microsomal epoxide hydrolase (mEH), levels of mEH mRNA, and the rate of mEH mRNA transcription were examined in hepatic and renal tissues at 4, 24, 44, and 56 weeks of age in male and 4, 14, 24, 34, and 44 weeks of age in female Sprague-Dawley rats. Immunoblot analyses revealed that hepatic mEH levels in males increased in an age-dependent manner, with a maximal increase (approximately 3-fold) being noted at 44 weeks of age, whereas the expression of hepatic mEH in females decreased significantly at 14 weeks of age or older, by approximately 70%s, compared with that of 4-week-old rats. Microsomes from kidney tissue failed to exhibit an age-dependent change in either sex. mEH mRNA levels were measured in total and poly(A)+ RNA isolated from hepatic and renal tissues. RNA blot hybridization analyses, probed with a 1.3-kilobase mEH cDNA, revealed that the levels of hepatic mEH mRNA in total RNA isolated from males were elevated approximately 1.5-, 2.8-, and 2.3-fold at 24, 44, and 56 weeks of age, respectively, relative to those at 4 weeks of age, whereas the levels of hepatic mEH mRNA in poly(A)+ RNA from males failed to change in an age-dependent manner. In contrast, the levels of hepatic mEH mRNA in either total or poly(A)+ RNA from female animals were dramatically decreased from 4 to 14 weeks of age, by approximately 90%. The suppressed levels of mEH mRNA in females were maintained at 24, 34, and 44 weeks of age (approximately 80%). However, the levels of renal mEH mRNA failed to change in an age-dependent manner in either sex, which was consistent with there being no change in the levels of mEH protein in kidney. In order to examine whether the gender-related maturational changes in hepatic mEH mRNA levels could result from transcriptional regulation, nuclear run-on assays were performed. The rate of hepatic mEH gene transcription failed to change in either males or females at the ages that exhibited significant changes in both mRNA levels and protein expression, suggesting that transcriptional regulation is not associated with the gender-dependent modulation of mEH mRNA levels during maturation.(ABSTRACT TRUNCATED AT 400 WORDS)
在雄性4周、24周、44周和56周龄以及雌性4周、14周、24周、34周和44周龄的Sprague-Dawley大鼠的肝脏和肾脏组织中,检测了微粒体环氧化物水解酶(mEH)的表达、mEH mRNA水平以及mEH mRNA转录速率。免疫印迹分析显示,雄性肝脏中mEH水平呈年龄依赖性增加,在44周龄时达到最大增幅(约3倍),而雌性肝脏中mEH的表达在14周龄及以上时显著下降,与4周龄大鼠相比,下降了约70%。肾脏组织的微粒体在两性中均未表现出年龄依赖性变化。从肝脏和肾脏组织中分离出总RNA和聚腺苷酸加尾(poly(A)+)RNA,测定mEH mRNA水平。用1.3千碱基的mEH cDNA进行RNA印迹杂交分析,结果显示,从雄性分离的总RNA中,肝脏mEH mRNA水平在24周、44周和56周龄时分别相对于4周龄时升高了约1.5倍、2.8倍和2.3倍,而雄性聚腺苷酸加尾RNA中肝脏mEH mRNA水平未呈年龄依赖性变化。相反,雌性动物总RNA或聚腺苷酸加尾RNA中肝脏mEH mRNA水平在4至14周龄时急剧下降,约90%。雌性中mEH mRNA的抑制水平在24周、34周和44周龄时维持在约80%。然而,肾脏mEH mRNA水平在两性中均未呈年龄依赖性变化,这与肾脏中mEH蛋白水平无变化一致。为了研究肝脏中mEH mRNA水平与性别相关的成熟变化是否由转录调控引起,进行了核转录分析。在mRNA水平和蛋白表达均有显著变化的年龄,雄性和雌性肝脏mEH基因转录速率均未改变,这表明转录调控与成熟过程中mEH mRNA水平的性别依赖性调节无关。(摘要截短至400字)