The potential for manipulating RNA with pentatricopeptide repeat proteins

被引:58
作者
Yagi, Yusuke [1 ]
Nakamura, Takahiro [1 ]
Small, Ian [2 ]
机构
[1] Kyushu Univ, Fac Agr, Fukuoka 8128581, Japan
[2] Univ Western Australia, Australian Res Council Ctr Excellence Plant Energ, Crawley 6009, Australia
基金
澳大利亚研究理事会;
关键词
PPR proteins; PUF proteins; transcription activator-like effectors; RNA binding; sequence-specific; synthetic biology; CYTOPLASMIC MALE-STERILITY; GENOME-WIDE ANALYSIS; MESSENGER-RNA; BINDING PROTEINS; PPR PROTEINS; MODULAR RECOGNITION; GENE-EXPRESSION; PLANT ORGANELLES; SPLICING FACTORS; EDITING FACTORS;
D O I
10.1111/tpj.12377
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The pentatricopeptide repeat (PPR) protein family, which is particularly prevalent in plants, includes many sequence-specific RNA-binding proteins involved in all aspects of organelle RNA metabolism, including RNA stability, processing, editing and translation. PPR proteins consist of a tandem array of 2-30 PPR motifs, each of which aligns to one nucleotide in the RNA target. The amino acid side chains at two or three specific positions in each motif confer nucleotide specificity in a predictable and programmable manner. Thus, PPR proteins appear to provide an extremely promising opportunity to create custom RNA-binding proteins with tailored specificity. We summarize recent progress in understanding RNA recognition by PPR proteins, with a particular focus on potential applications of PPR-based tools for manipulating RNA, and on the challenges that remain to be overcome before these tools may be routinely used by the scientific community.
引用
收藏
页码:772 / 782
页数:11
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