The identification of an endonuclease that cleaves within an HuR binding site in mRNA

被引:35
作者
Zhao, ZQ [1 ]
Chang, FC [1 ]
Furneaux, HM [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Program Mol Pharmacol & Therapeut, New York, NY 10021 USA
关键词
D O I
10.1093/nar/28.14.2695
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Messenger RNAs (mRNAs) that contain U-rich elements are targeted for rapid decay. Selective inhibition of this decay results in a rapid increase in steady state level. Thus, this is an important regulatory step in gene expression. Previously, we have found that these mRNAs are selectively stabilized by a specific mRNA binding protein called HuR. The mechanism of action of HuR is not well understood. It has been postulated that HuR stabilizes mRNA by the displacement or inhibition of factors that specifically cleave or deadenylate these mRNAs. In this paper, we report the identification and characterization of a novel endonuclease that cleaves within an HuR binding site in p27kip1 mRNA. The specificity of this endonuclease and its inhibition by HuR argue for it playing a role in the postranscriptional regulation of gene expression.
引用
收藏
页码:2695 / 2701
页数:7
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