Porvari K, Kurkela R, Kivinen A, Vihko P
Biocenter Oulu, University of Oulu, Finland.
Biochem Biophys Res Commun. 1995 Aug 24;213(3):861-8. doi: 10.1006/bbrc.1995.2208.
Steady-state levels of the mRNAs encoding rat prostatic acid phosphatase (rPAP) were measured from the ventral prostate of rats after castration and testosterone replacement. The longest and the most abundant mRNA molecule (4.9 kb) of the rPAP gene was quite resistant to the hormonal status of the prostate, whereas its medium-sized transcript (2.3 kb) and the shortest one (1.5 kb) were up-regulated by androgens. For comparison, we also analyzed the prostatic mRNA levels of rat lysosomal acid phosphatase (rLAP), whose gene expression is not considered to be hormonally dependent. Only modest variation was observed in the rLAP transcript after androgen withdrawal and replacement. Corresponding protein level investigations are analogous with our regulation studies, particularly in the case of 1.5-kb rPAP mRNA.
在大鼠去势及睾酮替代后,从大鼠腹侧前列腺中测量了编码大鼠前列腺酸性磷酸酶(rPAP)的mRNA的稳态水平。rPAP基因最长且最丰富的mRNA分子(4.9 kb)对前列腺的激素状态相当不敏感,而其中等大小的转录本(2.3 kb)和最短的转录本(1.5 kb)则受雄激素上调。为作比较,我们还分析了大鼠溶酶体酸性磷酸酶(rLAP)的前列腺mRNA水平,其基因表达不被认为依赖激素。在雄激素撤除及替代后,rLAP转录本仅观察到适度变化。相应的蛋白质水平研究与我们的调控研究相似,特别是在1.5 kb rPAP mRNA的情况下。