首页> 美国卫生研究院文献>Nucleic Acids Research >The adenovirus L4-22K protein regulates transcription and RNA splicing via a sequence-specific single-stranded RNA binding
【2h】

The adenovirus L4-22K protein regulates transcription and RNA splicing via a sequence-specific single-stranded RNA binding

机译:腺病毒L4-22K蛋白通过序列特异性单链RNA结合调节转录和RNA剪接

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 adenovirus L4-22K protein both activates and suppresses transcription from the adenovirus major late promoter (MLP) by binding to DNA elements located downstream of the MLP transcriptional start site: the so-called DE element (positive) and the R1 region (negative). Here we show that L4-22K preferentially binds to the RNA form of the R1 region, both to the double-stranded RNA and the single-stranded RNA of the same polarity as the nascent MLP transcript. Further, L4-22K binds to a 5΄-CAAA-3΄ motif in the single-stranded RNA, which is identical to the sequence motif characterized for L4-22K DNA binding. L4-22K binding to single-stranded RNA results in an enhancement of U1 snRNA recruitment to the major late first leader 5΄ splice site. This increase in U1 snRNA binding results in a suppression of MLP transcription and a concurrent stimulation of major late first intron splicing.
机译:腺病毒L4-22K蛋白通过与位于MLP转录起始位点下游的DNA元件结合而激活和抑制从腺病毒主要晚期启动子(MLP)转录:所谓的DE元件(正)和R1区域(负) 。在这里,我们显示L4-22K优先结合R1区域的RNA形式,与新生MLP转录物具有相同极性的双链RNA和单链RNA都结合。此外,L4-22K与单链RNA中的5′-CAAA-3′基序结合,其与表征L4-22K DNA结合的序列基序相同。 L4-22K与单链RNA的结合导致U1 snRNA募集到主要的晚期第一个前导5'剪接位点。 U1 snRNA结合的这种增加导致MLP转录的抑制和主要晚期第一内含子剪接的同时刺激。

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