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Nuclear binding of oestradiol-17β and induction of protein synthesis in the rat uterus during postnatal development

机译:产后发育期大鼠子宫中雌二醇-17β的核结合及蛋白合成的诱导

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摘要

1. The uterine response to a single injection of oestradiol-17β during postnatal development of the rat was studied with respect to (i) nuclear binding of oestradiol-17β; (ii) induction of the synthesis of a specific cytoplasmic protein (`induced protein' of Gorski); (iii) rate of incorporation of 3H-labelled amino acids into total protein and into nuclear acid-soluble and acid-insoluble protein; and (iv) rate of [3H]thymidine incorporation into DNA. 2. Specific nuclear binding of oestradiol-17β could be demonstrated even at birth. Administration of oestradiol-17β in vivo caused a significant increase in the number of nuclear binding sites in rats aged 10 days or older. 3. A rapid method is described for the detection of the `induced protein', based on cellulose acetate electrophoresis. Induction of this protein could be demonstrated at the age of 10, 15 and 20 days, but not in 5-day-old rats. 4. In 20-day-old rats the rate of 3H-labelled amino acid incorporation into protein increased by 3h after oestradiol administration. Incorporation into the different protein fractions reached peak values asynchronously: at 3–4h for acid-insoluble nuclear protein, at 6h for total protein and at about 12h for acid-soluble protein. 5. Treatment with oestradiol failed to stimulate amino acid incorporation into protein in 5- or 10-day-old rats; at the age of 15 to 30 days the hormone caused a significant increase in incorporation into total protein and into both types of nuclear protein. 6. Since the capacity for nuclear binding of oestradiol and for synthesis of the induced protein is demonstrable in the rat uterus before it acquires the ability to respond to the hormone with enhanced general protein synthesis and DNA synthesis, it appears that nuclear binding and the synthesis of the induced protein may be necessary but not sufficient conditions for the trophic action of oestradiol.
机译:1.研究大鼠在出生后发育过程中单次注射雌二醇17β的子宫反应,其中(i)雌二醇17β的核结合; (ii)诱导特定胞质蛋白(Gorski的“诱导蛋白”)的合成; (iii) 3 H标记的氨基酸掺入总蛋白以及可溶于核酸和不溶于酸的蛋白的比率; (iv)[ 3 H]胸苷掺入DNA的速率。 2.即使在出生时,也可以证明oestradiol-17β的特异性核结合。体内施用雌二醇-17β导致10天或更老的大鼠的核结合位点数量显着增加。 3.描述了一种基于醋酸纤维素电泳的快速检测“诱导蛋白”的方法。可以在10、15和20天的年龄证明这种蛋白的诱导,但在5天大的大鼠中则没有。 4.在雌二醇给药3小时后,在20日龄大鼠中, 3 H标记的氨基酸掺入蛋白质的速率增加。掺入不同蛋白质部分的过程异步达到峰值:酸不溶性核蛋白在3-4小时,总蛋白在6h和酸溶性蛋白在12h左右。 5.用雌二醇治疗未能刺激5日龄或10日龄大鼠中的氨基酸掺入蛋白质。在15至30天的年龄时,激素会导致总蛋白和两种核蛋白的掺入量显着增加。 6.由于在大鼠子宫内可证明雌二醇的核结合能力和诱导蛋白的合成能力,在其获得对激素反应的能力之前,具有增强的一般蛋白质合成和DNA合成能力,因此看来核结合和合成对于雌二醇的营养作用,诱导蛋白的制备可能是必要的,但不是充分的条件。

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