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雌二醇对大鼠子宫DNA依赖性RNA聚合酶的作用。对可溶性酶的研究。

Effect of estradiol on rat uterus DNA-dependent RNA polymerases. Studies on solubilized enzymes.

作者信息

Courvalin J C, Bouton M M, Baulieu E E, Nuret P, Chambon P

出版信息

J Biol Chem. 1976 Aug 25;251(16):4843-9.

PMID:956166
Abstract

DNA-dependent RNA polymerases of immature and castrated rat uteri were studied after estradiol administration. The enzymes were solubilized from either whole uterus homogenate or nuclei and their activities were measured on an exogenous DNA template. alpha-Amanitin was used to distinguish alpha-amanitin-resistant from alpha-amanitin-senitive forms of the enzyme. The number of alpha-amanitin-sensitive RNA polymerase molecules was measured by a binding assay using labeled amanitin. In the first series of experiments RNA polymerases were solubilized from whole uterus homogenate. alpha-Amanitin-sensitive and -resistant activities were constant during the first 6 hours after estradiol treatment, followed by a late and moderate increase in their activities (50% at 12 hours for the resistant form and 40% at 24 hours for the sensitive form). The number of sensitive polymerase molecules evolved in an identical manner to its activity (+40% at 24 hours), suggesting that the increase in activity is due to the synthesis of new enzyme molecules. For both forms, no diffusible stimulatory factor was detected in the uterus of hormone-treated animals. In the second series of experiments, disrupted nuclei were washed with 0.15 M (NH4)2SO4 in order to release only enzyme molecules which were not firmly bound to DNA in a transcription complex. The amount of the sensitive form of polymerase which remains firmly bound to chromatin, was constant for 6 hours after estradiol administration and was doubled by 24 hours. The firmly bound alpha-amanitin-resistant activity was solubilized and was measured in the presence of an exogenous template. There was a progressive increase in activity first detectable in 1 to 2 hours, amounting to 50% at 6 hours and 100% at 24 hours. The reported results show that during the first 6 hours of hormone treatment: (a) the total content of RNA polymerases remains unchanged in the uterus; (b) the number of alpha-amanitin resistant molecules tightly bound to DNA increases progressively while the alpha-amanitin sensitive remains constant. At a later time (24 hours), an increase is observed both for the total amount of enzymes and for their fraction engaged in a transcription complex.

摘要

在给予雌二醇后,对未成熟和阉割大鼠子宫的DNA依赖性RNA聚合酶进行了研究。这些酶从全子宫匀浆或细胞核中溶解出来,并在体外DNA模板上测定其活性。使用α-鹅膏蕈碱来区分对α-鹅膏蕈碱有抗性和敏感的酶形式。通过使用标记的鹅膏蕈碱的结合测定法来测量对α-鹅膏蕈碱敏感的RNA聚合酶分子的数量。在第一系列实验中,从全子宫匀浆中溶解RNA聚合酶。在雌二醇处理后的最初6小时内,对α-鹅膏蕈碱敏感和抗性的活性保持恒定,随后其活性出现后期适度增加(抗性形式在12小时时增加50%,敏感形式在24小时时增加40%)。敏感聚合酶分子的数量与其活性以相同方式变化(在24小时时增加40%),这表明活性增加是由于新酶分子的合成。对于这两种形式,在激素处理动物的子宫中均未检测到可扩散的刺激因子。在第二系列实验中,用0.15M硫酸铵洗涤破碎的细胞核,以便仅释放未牢固结合在转录复合物中的DNA上的酶分子。在给予雌二醇后6小时内,与染色质牢固结合的聚合酶敏感形式的量保持恒定,并在24小时时增加一倍。将牢固结合的对α-鹅膏蕈碱有抗性的活性溶解,并在存在体外模板的情况下进行测量。活性在1至2小时时首次可检测到逐渐增加,在6小时时达到50%,在24小时时达到100%。报告的结果表明,在激素处理的最初6小时内:(a)子宫中RNA聚合酶的总含量保持不变;(b)紧密结合在DNA上的对α-鹅膏蕈碱有抗性的分子数量逐渐增加,而对α-鹅膏蕈碱敏感的分子数量保持恒定。在稍后的时间(24小时),观察到酶的总量及其参与转录复合物的部分均增加。

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