Incorporation of pseudouridine into mRNA enhances translation by diminishing PKR activation

被引:501
作者
Anderson, Bart R. [2 ]
Muramatsu, Hiromi [1 ]
Nallagatla, Subba R. [3 ]
Bevilacqua, Philip C. [3 ]
Sansing, Lauren H. [4 ]
Weissman, Drew [2 ]
Kariko, Katalin [1 ]
机构
[1] Univ Penn, Dept Neurosurg, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[3] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[4] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-KINASE PKR; DOUBLE-STRANDED-RNA; TOLL-LIKE RECEPTORS; TREATED HELA-CELLS; 2'; 5'-OLIGO(A); POLYMERASE; INTERFERON INDUCTION; THERMAL-STABILITY; BINDING DOMAIN; INHIBITION; DUPLEXES;
D O I
10.1093/nar/gkq347
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Previous studies have shown that the translation level of in vitro transcribed messenger RNA (mRNA) is enhanced when its uridines are replaced with pseudouridines; however, the reason for this enhancement has not been identified. Here, we demonstrate that in vitro transcripts containing uridine activate RNA-dependent protein kinase (PKR), which then phosphorylates translation initiation factor 2-alpha (eIF-2 alpha), and inhibits translation. In contrast, in vitro transcribed mRNAs containing pseudouridine activate PKR to a lesser degree, and translation of pseudouridine-containing mRNAs is not repressed. RNA pull-down assays demonstrate that mRNA containing uridine is bound by PKR more efficiently than mRNA with pseudouridine. Finally, the role of PKR is validated by showing that pseudouridine- and uridine-containing RNAs were translated equally in PKR knockout cells. These results indicate that the enhanced translation of mRNAs containing pseudouridine, compared to those containing uridine, is mediated by decreased activation of PKR.
引用
收藏
页码:5884 / 5892
页数:9
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