Synthetic PPR proteins as tools for sequence-specific targeting of RNA

被引:9
|
作者
McDowell, Rose [1 ]
Small, Ian [1 ]
Bond, Charles S. [2 ]
机构
[1] Univ Western Australia, Australian Res Council Ctr Excellence Plant Energ, Sch Mol Sci, 35 Stirling Highway, Crawley, WA 6009, Australia
[2] Univ Western Australia, Sch Mol Sci, 35 Stirling Highway, Crawley, WA 6009, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
PENTATRICOPEPTIDE REPEAT PROTEINS; BINDING PROTEINS; FLUORESCENCE COMPLEMENTATION; MODULAR RECOGNITION; EDITING FACTORS; MALE-STERILITY; IDENTIFICATION; DESIGN; PLANTS; DOMAIN;
D O I
10.1016/j.ymeth.2022.10.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In native systems, gene expression is regulated by RNA binding proteins. Such proteins have been the target of a great deal of recent research interest, due to the potential for harnessing these regulatory effects for the construction of new biotechnological tools. In particular, focus has been targeted on building synthetic RNA binding proteins for sequence-specific targeting of new RNA transcripts. Pentatricopeptide repeat (PPR) proteins make compelling candidates as synthetic RNA binding proteins to target and bind RNA transcripts of interest, due to their defined RNA binding "code ", modular structure, and native capability to deliver catalytic C-terminal domains. In this review, we present a summary of up-to-date understanding of RNA site recognition by PPR proteins, progress towards the design of synthetic PPR proteins for RNA targeting in vitro and in vivo, highlight key areas for further research around these proteins and present an outlook for future applications for synthetic PPR proteins as biotechnological tools.
引用
收藏
页码:19 / 26
页数:8
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