首页> 美国卫生研究院文献>Cancer Science >Activation of the Mouse Proliferating Cell Nuclear Antigen Gene Promoter by Adenovirus Type 12 E1A Proteins
【2h】

Activation of the Mouse Proliferating Cell Nuclear Antigen Gene Promoter by Adenovirus Type 12 E1A Proteins

机译:腺病毒12型E1A蛋白激活小鼠增殖细胞核抗原基因启动子。

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

A plasmid carrying the 5′‐flanking region (– 1584 to + 47 with respect to the transcription initiation site) of the mouse proliferating cell nuclear antigen (PCNA) gene was fused with the chloramphenicol acetyltransferase (CAT) gene, and then cotransfected into mouse N18TG2 cells with expression plasmids for the adenovirus type 12 E1 genes. Expression of E1A gene products elevated the CAT expression by 5‐ to 9‐fold, but expression of the E1B gene product did not. RNase protection analysis revealed that the activation of the PCNA gene promoter by E1A was at the transcription step. Both the 13S E1A and the 12S E1A activated the PCNA gene promoter, indicating that the activation domain of El A resides in a common region(s) of 13S and 12S El A products. The major target region of El A was mapped within the 68 base‐pair region (‐21 to +47) of the PCNA gene, which includes consensus sequences for transcription factors PEA3 and E2P, although the upstream region (–83 to – 21) including ATF(CREB)‐binding consensus had an additional effect in the transactivation.
机译:将带有小鼠增殖细胞核抗原(PCNA)基因5'侧翼区域(相对于转录起始位点为– 1584至+ 47)的质粒与氯霉素乙酰转移酶(CAT)基因融合,然后共转染到小鼠体内N18TG2细胞,带有用于12型腺病毒E1基因的表达质粒。 E1A基因产物的表达使CAT表达提高了5到9倍,但E1B基因产物的表达却没有。 RNase保护分析表明,E1A对PCNA基因启动子的激活处于转录步骤。 13S E1A和12S E1A均激活了PCNA基因启动子,表明El A的激活域位于13S和12S El A产物的公共区域。 El A的主要靶标区域位于PCNA基因的68个碱基对区域(–21至+47)内,其中包括转录因子PEA3和E2P的共有序列,尽管上游区域(–83至– 21)包括与ATF(CREB)结合的共识在反式激活中具有附加作用。

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