首页> 美国卫生研究院文献>Molecular and Cellular Biology >Modulation of novel-length DOPA decarboxylase transcripts by 20-OH-ecdysone in a Drosophila melanogaster Kc cell subline.
【2h】

Modulation of novel-length DOPA decarboxylase transcripts by 20-OH-ecdysone in a Drosophila melanogaster Kc cell subline.

机译:果蝇黑果Kc细胞亚系中20-OH-蜕皮激素对新型长度DOPA脱羧酶转录产物的调节。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The induction of DOPA decarboxylase (DDC) activity by 20-OH-ecdysone (20-OHE) in a subline of Drosophila melanogaster Kc cells was investigated. Cells cultured in the continuous presence of the steroid hormone exhibited a 96-h temporal lag prior to a peak of DDC enzyme activity while arrested in the G2 phase of the cell cycle. The concentration of Ddc RNA increased sixfold between 72 and 96 h after initial exposure to hormone. Similarly, this increase was correlated temporally with a 26-fold increase in DDC enzyme activity. The Kc Ddc primary transcript, processing intermediate, and mature mRNA all were approximately 500 nucleotides longer than the corresponding transcripts observed for newly eclosed adult D. melanogaster. In vitro translation of poly(A)+ RNA from Kc cells resulted in an immunoprecipitable polypeptide which exhibited similar mobility on sodium dodecyl sulfate gels to that of DDC synthesized in vitro by larval epidermal poly(A)+ RNA.
机译:研究了果蝇Kc细胞亚系中20-OH-蜕皮激素(20-OHE)对DOPA脱羧酶(DDC)活性的诱导作用。在类固醇激素持续存在下培养的细胞在DDC酶活性达到峰值之前表现出96小时的时间滞后,同时停滞在细胞周期的G2期。最初接触激素后72至96小时,Ddc RNA的浓度增加了六倍。同样,这种增加在时间上与DDC酶活性的26倍增加相关。 Kc Ddc初级转录本,加工中间产物和成熟mRNA均比新封闭的成年D. melanogaster观察到的相应转录本长约500个核苷酸。来自Kc细胞的poly(A)+ RNA的体外翻译产生了一种可免疫沉淀的多肽,该多肽在十二烷基硫酸钠凝胶上显示出与幼虫表皮poly(A)+ RNA体外合成的DDC相似的迁移率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号