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对脱氧核糖核酸具有高亲和力的前列腺蛋白的雄激素调节。前列腺脱氧核糖核酸解旋蛋白的证据。

The androgenic regulation of prostate proteins with a high affinity for deoxyribonucleic acid. Evidence for a prostate deoxyribonucleic acid-unwinding protein.

作者信息

Mainwaring W I, Rennie P S, Keen J

出版信息

Biochem J. 1976 May 15;156(2):253-64. doi: 10.1042/bj1560253.

Abstract
  1. When testosterone is injected into castrated rats in vivo, a significant increase in the incorporation of [35S]methionine into prostate proteins may be detected under conditions in vitro. 2. Studies based on DNA-cellulose chromatography show that the synthesis of prostate proteins with a high affinity for DNA is particularly enhanced by androgenic stimulation. 3. These changes in protein synthesis are negated when the anti-androgen, cyproterone acetate, is administered concomitantly with testosterone in vivo. 4. Two assays were developed for measuring the strand separation of prostate DNA; first, the retention of 3H-labelled native DNA on nitrocellulose membranes, and second, the activation of native DNA as a template for 9S prostate DNA polymerase. On the basis of these criteria, DNA-unwinding activity is present in the prostate gland and it is regulated by androgens in a steroid-and tissue-specific manner. 5. The results are discussed in the context of the mechanism of action of androgens, particularly since the changes provoked in DNA-unwinding activity by androgens precede the onset of DNA replication and mitosis.
摘要
  1. 当在体内给去势大鼠注射睾酮时,在体外条件下可检测到[35S]甲硫氨酸掺入前列腺蛋白的量显著增加。2. 基于DNA - 纤维素色谱法的研究表明,对DNA具有高亲和力的前列腺蛋白的合成特别受到雄激素刺激的增强。3. 当在体内将抗雄激素药物醋酸环丙孕酮与睾酮同时给药时,蛋白质合成的这些变化被消除。4. 开发了两种测定前列腺DNA链分离的方法;第一种是3H标记的天然DNA在硝酸纤维素膜上的保留,第二种是天然DNA作为9S前列腺DNA聚合酶模板的活化。基于这些标准,前列腺中存在DNA解旋活性,并且它以类固醇和组织特异性方式受雄激素调节。5. 在雄激素作用机制的背景下讨论了这些结果,特别是因为雄激素引起的DNA解旋活性变化先于DNA复制和有丝分裂的开始。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1edc/1163744/097f2211498e/biochemj00533-0081-a.jpg

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