The editing enzyme ADAR1 and the mRNA surveillance protein hUpf1 interact in the cell nucleus

被引:40
作者
Agranat, Lily [1 ]
Raitskin, Oleg [1 ]
Sperling, Joseph [2 ]
Sperling, Ruth [1 ]
机构
[1] Hebrew Univ Jerusalem, Dept Genet, IL-91904 Jerusalem, Israel
[2] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
关键词
RNAi; supraspliceosomes; posttranscriptional regulation; nuclear complexes; cross-linking;
D O I
10.1073/pnas.0710576105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Posttranscriptional regulation is an important step in the regulation of gene expression. In this article, we show an unexpected connection between two proteins that participate in different processes of posttranscriptional regulation that ensures the production of functional mRNA molecules. Specifically, we show that the A-to-I RNA editing protein adenosine deaminase that acts on RNA 1 (ADAR1) and the human Upf1 (hUpf1) protein involved in RNA surveillance are found associated within nuclear RNA-splicing complexes. A potential functional role for this association was revealed by RNAi-mediated down-regulation of ADAR1, which was accompanied by up-regulation of a number of genes previously shown to undergo A-to-I editing in A/u repeats and to be downregulated by hUpf1. This study suggests a regulatory pathway by a combination of ADAR1 A-to-I editing enzyme and RNA degradation presumably with the aid of hUpf1.
引用
收藏
页码:5028 / 5033
页数:6
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