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果蝇细胞系中的蜕皮类固醇诱导多肽

Ecdysteroid-inducible polypeptides in a Drosophila cell line.

作者信息

Savakis C, Demetri G, Cherbas P

出版信息

Cell. 1980 Dec;22(3):665-74. doi: 10.1016/0092-8674(80)90542-5.

Abstract

In the Drosophila melanogaster cell line Kc-H, ecdysteroid hormone treatment causes increased relative synthesis of three ecdysteroid-inducible polypeptides (EIPs), named according to their molecular weights (in kilodaltons) EIP 40, EIP 29 and EIP 28. Increased synthesis of the EIPs is detectable within 45 min (EIP 28) or 75 min (EIPs 40 and 29), is maximal at 4-8 hr and continues for almost 2 days. During this period no other major changes in protein synthesis are discernible using one-dimensional gels. At maximum, EIP 28 synthesis is elevated at least 10 fold above its basal level, and EIPs 40 and 29 somewhat less. EIP induction is ecdysteroid-specific and is detectable in the presence of 10(-8) M 20-hydroxyecdysone. It does not occur in hormone-resistant cells. Apparently identical polypeptides are inducible in another ecdysteroid-responsive cell line, Schneider's line 3. Because EIP synthesis is an early and substantial response to ecdysteroids, this is a promising system for the study of steroid hormone action.

摘要

在果蝇细胞系Kc-H中,蜕皮甾体激素处理会导致三种蜕皮甾体诱导多肽(EIPs)的相对合成增加,这三种多肽根据其分子量(千道尔顿)分别命名为EIP 40、EIP 29和EIP 28。EIPs合成增加在45分钟(EIP 28)或75分钟(EIP 40和EIP 29)内即可检测到,在4 - 8小时达到最大值,并持续近2天。在此期间,使用一维凝胶无法看出蛋白质合成有其他主要变化。在最大值时,EIP 28的合成比其基础水平至少提高了10倍,EIP 40和EIP 29的提高幅度稍小。EIP诱导具有蜕皮甾体特异性,在存在10^(-8) M 20-羟基蜕皮酮的情况下即可检测到。在激素抗性细胞中不会发生这种情况。在另一种蜕皮甾体反应性细胞系施耐德3号线中可诱导出明显相同的多肽。由于EIP合成是对蜕皮甾体的早期且显著的反应,这是一个研究甾体激素作用的有前景的系统。

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