Pentatricopeptide Repeat Proteins with the DYW Motif Have Distinct Molecular Functions in RNA Editing and RNA Cleavage in Arabidopsis Chloroplasts

被引:196
作者
Okuda, Kenji [1 ]
Chateigner-Boutin, Anne-Laure [2 ]
Nakamura, Takahiro [3 ,4 ]
Delannoy, Etienne [2 ]
Sugita, Mamoru [5 ]
Myouga, Fumiyoshi [6 ]
Motohashi, Reiko [7 ]
Shinozaki, Kazuo [6 ]
Small, Ian [2 ]
Shikanaia, Toshiharu [1 ]
机构
[1] Kyoto Univ, Grad Sch Sci, Dept Bot, Kyoto 6068502, Japan
[2] Univ Western Australia, Australian Res Council, Ctr Excellence Plant Energy Biol, Perth, WA 6009, Australia
[3] Kyushu Univ, Grad Sch Agr, Org Promot Adv Res, Fukuoka 8128151, Japan
[4] PRESTO, Kawaguchi, Saitama 3320012, Japan
[5] Nagoya Univ, Ctr Gene Res, Nagoya, Aichi 4648602, Japan
[6] RIKEN, Plant Sci Ctr, Plant Genome Network Res Team, Yokohama, Kanagawa 2030045, Japan
[7] Shizuoka Univ, Fac Agr, Shizuoka 4228529, Japan
基金
澳大利亚研究理事会;
关键词
NUCLEUS-ENCODED FACTOR; CYTIDINE DEAMINASE; MESSENGER-RNA; PPR PROTEINS; MITOCHONDRIAL; REVEALS; SITE; EXPRESSION; ENZYME; DOMAIN;
D O I
10.1105/tpc.108.064667
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
The plant-specific DYW subclass of pentatricopeptide repeat proteins has been postulated to be involved in RNA editing of organelle transcripts. We discovered that the DYW proteins CHLORORESPIRATORY REDUCTION22 (CRR22) and CRR28 are required for editing of multiple plastid transcripts but that their DYW motifs are dispensable for editing activity in vivo. Replacement of the DYW motifs of CRR22 and CRR28 by that of CRR2, which has been shown to be capable of endonucleolytic cleavage, blocks the editing activity of both proteins. In return, the DYW motifs of neither CRR22 nor CRR28 can functionally replace that of CRR2. We propose that different DYW family members have acquired distinct functions in the divergent processes of RNA maturation, including RNA cleavage and RNA editing.
引用
收藏
页码:146 / 156
页数:11
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