Dodd J G, Kreis C, Sheppard P C, Hamel A, Matusik R J
Mol Cell Endocrinol. 1986 Oct;47(3):191-200. doi: 10.1016/0303-7207(86)90112-7.
The androgen dependence of a highly abundant mRNA found in the rat dorsolateral prostate and seminal vesicles has been investigated using a complementary DNA clone from a rat dorsal prostate library. The 1.5 kilobase (kb) mRNA codes for a 52 000 Da translation product which is processed to 49 000 Da in the presence of microsomal membranes. This product appears to correspond to the previously described SVS II protein secreted by rat seminal vesicles and can be immunoprecipitated with anti-SVS II antiserum. Dot hybridization assays indicated that the mRNA is abundant in the dorsal and lateral prostate glands and in seminal vesicles but not in the ventral prostate, coagulating gland or other non-accessory sex tissues. Castration of mature male rats reduces the 1.5 kb mRNA 10-fold in the seminal vesicles and 7-fold in the dorsolateral prostate in 9 days. Androgen administration to one-week castrates returned the mRNA level to normal in both tissues within 48 h. The levels of the 1.5 kb mRNA are very similar in the dorsolateral prostate and seminal vesicles at maturity but distinct patterns of developmental regulation of this gene exist in the two tissues. Between 3 and 6 weeks of age, the level of the 1.5 kb mRNA increases approximately 3-fold in the dorsolateral prostate while the increase in the seminal vesicles is more than 600-fold.
利用大鼠背侧前列腺文库中的互补DNA克隆,对在大鼠背外侧前列腺和精囊中发现的一种高丰度mRNA的雄激素依赖性进行了研究。这种1.5千碱基(kb)的mRNA编码一种52000道尔顿的翻译产物,在微粒体膜存在的情况下,该产物会被加工成49000道尔顿。该产物似乎对应于先前描述的由大鼠精囊分泌的SVS II蛋白,并且可以用抗SVS II抗血清进行免疫沉淀。斑点杂交分析表明,这种mRNA在背侧和外侧前列腺以及精囊中含量丰富,但在腹侧前列腺、凝固腺或其他非附属生殖组织中则没有。对成熟雄性大鼠进行去势手术,9天后精囊中1.5 kb的mRNA减少10倍,背外侧前列腺中减少7倍。对去势一周的大鼠给予雄激素,48小时内两个组织中的mRNA水平均恢复正常。成熟时,背外侧前列腺和精囊中1.5 kb mRNA的水平非常相似,但该基因在这两个组织中的发育调控模式不同。在3至6周龄之间,背外侧前列腺中1.5 kb mRNA的水平增加约3倍,而精囊中增加超过600倍。