4.8 Article

Technology Targeted pseudouridylation: An approach for suppressing nonsense mutations in disease genes

期刊

MOLECULAR CELL
卷 83, 期 4, 页码 637-+

出版社

CELL PRESS
DOI: 10.1016/j.molcel.2023.01.009

关键词

-

向作者/读者索取更多资源

This study presents a targeted PTC pseudouridylation method to suppress nonsense mutations. It can inhibit nonsense-mediated mRNA decay and promote PTC readthrough. It can also be used in combination with antibiotic treatment to improve the suppression effect. Transfection of a designer guide RNA gene can also achieve nonsense suppression in disease model cell lines carrying chromosomal PTC.
Nonsense mutations create premature termination codons (PTCs), activating the nonsense-mediated mRNA decay (NMD) pathway to degrade most PTC-containing mRNAs. The undegraded mRNA is translated, but translation terminates at the PTC, leading to no production of the full-length protein. This work presents targeted PTC pseudouridylation, an approach for nonsense suppression in human cells. Specifically, an artificial box H/ACA guide RNA designed to target the mRNA PTC can suppress both NMD and premature translation termination in various sequence contexts. Targeted pseudouridylation exhibits a level of suppression comparable with that of aminoglycoside antibiotic treatments. When targeted pseudouridylation is combined with antibiotic treatment, a much higher level of suppression is observed. Transfection of a disease model cell line (carrying a chromosomal PTC) with a designer guide RNA gene targeting the PTC also leads to nonsense suppression. Thus, targeted pseudouridylation is an RNA-directed gene-specific approach that suppresses NMD and concurrently promotes PTC readthrough.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据