...
首页> 外文期刊>Molecular cell >U1 snRNP Inhibits Pr-mRNA Polyadenylation through a Direct Interaction between U1 70K and Poly(A) Polymerase
【24h】

U1 snRNP Inhibits Pr-mRNA Polyadenylation through a Direct Interaction between U1 70K and Poly(A) Polymerase

机译:U1 snRNP通过U1 70K和Poly(A)聚合酶之间的直接相互作用抑制Pr-mRNA聚腺苷酸化

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

It has previously been shown in vivo that bovine papillomavirus represses its late gene expression via a 5' splice site sequence located upstream of the late poly-adenylation signal. Here, the mechanism of repression is determined by in vitro analysis. U1 snRNP binding to the 5' splice site results in inhibition of polyadenylation via a direct interaction with poly(A) polymerase (PAP). Although the inhibitory mechanism is similar to that used in U1A autoregulation, U1A within the U1 snRNP does not contribute to PAP inhibition. Instead the U1 70K protein, when bound to U1 snRNA, both interacts with and inhibits PAP. Conservation of the U1 70K inhibitory domains suggests that polyadenylation regulation via PAP inhibition may be more widespread than previously thought.
机译:先前已经在体内表明牛乳头瘤病毒通过位于晚期聚腺苷酸化信号上游的5'剪接位点序列抑制其晚期基因表达。在这里,抑制机制是通过体外分析确定的。 U1 snRNP绑定到5'剪接位点导致通过与聚(A)聚合酶(PAP)的直接相互作用抑制聚腺苷酸化。尽管抑制机制与U1A自动调节中使用的抑制机制相似,但U1 snRNP中的U1A不会导致PAP抑制。相反,当与U1 snRNA结合时,U1 70K蛋白既与PAP相互作用也抑制PAP。 U1 70K抑制域的保守表明通过PAP抑制的聚腺苷酸调节作用可能比以前认为的更为广泛。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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