共查询到20条相似文献,搜索用时 62 毫秒
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Yan-Zhuo Yang Shuo Ding Xin-Yuan Liu Chunhui Xu Feng Sun Bao-Cai Tan 《植物学报(英文版)》2023,65(11):2456-2468
RNA helicases participate in nearly all aspects of RNA metabolism by rearranging RNAs or RNA–protein complexes in an adenosine triphosphatedependent manner. Due to the large RNA helicase families in plants, the precise roles of many RNA helicases in plant physiology and development remain to be clarified. Here, we show that mutations in maize(Zea mays) DEAD-box RNA helicase48(Zm RH48) impair the splicing of mitochondrial introns, mitochondrial complex biosynthesis,and seed development. Loss of Z... 相似文献
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AEF1/MPR25 is implicated in RNA editing of plastid atpF and mitochondrial nad5, and also promotes atpF splicing in Arabidopsis and rice 下载免费PDF全文
Aaron Yap Peter Kindgren Catherine Colas des Francs‐Small Tomohiko Kazama Sandra K. Tanz Kinya Toriyama Ian Small 《The Plant journal : for cell and molecular biology》2015,81(5):661-669
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Emp10 encodes a mitochondrial PPR protein that affects the cis‐splicing of nad2 intron 1 and seed development in maize 下载免费PDF全文
Manjun Cai Shuzhen Li Feng Sun Qin Sun Hailiang Zhao Xuemei Ren Yanxin Zhao Bao‐Cai Tan Zuxin Zhang Fazhan Qiu 《The Plant journal : for cell and molecular biology》2017,91(1):132-144
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Sosso D Mbelo S Vernoud V Gendrot G Dedieu A Chambrier P Dauzat M Heurtevin L Guyon V Takenaka M Rogowsky PM 《The Plant cell》2012,24(2):676-691
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Rüdinger M Szövényi P Rensing SA Knoop V 《The Plant journal : for cell and molecular biology》2011,67(2):370-380
The plant‐specific pentatricopeptide repeat (PPR) proteins with variable PPR repeat lengths (PLS‐type) and protein extensions up to the carboxyterminal DYW domain have received attention as specific recognition factors for the C‐to‐U type of RNA editing events in plant organelles. Here, we report a DYW‐protein knockout in the model plant Physcomitrella patens specifically affecting mitochondrial RNA editing positions cox1eU755SL and rps14eU137SL. Assignment of DYW proteins and RNA editing sites might best be corroborated by data from a taxon with a slightly different, yet similarly manageable low number of editing sites and DYW proteins. To this end we investigated the mitochondrial editing status of the related funariid moss Funaria hygrometrica. We find that: (i) Funaria lacks three mitochondrial RNA editing positions present in Physcomitrella, (ii) that F. hygrometrica cDNA sequence data identify nine DYW proteins as clear orthologues of their P. patens counterparts, and (iii) that the ‘missing’ 10th DYW protein in F. hygrometrica is responsible for two mitochondrial editing sites in P. patens lacking in F. hygrometrica (nad3eU230SL, nad4eU272SL). Interestingly, the third site of RNA editing missing in F. hygrometrica (rps14eU137SL) is addressed by the DYW protein characterized here and the presence of its orthologue in F. hygrometrica is explained through its simultaneous action on site cox1eU755SL conserved in both mosses. 相似文献
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Barbara Härtel Anja Zehrmann Daniil Verbitskiy Johannes A. van der Merwe Axel Brennicke Mizuki Takenaka 《Plant molecular biology》2013,81(4-5):337-346
A forwards genetic screen of a chemically mutated plant population identified mitochondrial RNA editing factor 10 (MEF10) in Arabidopsis thaliana. MEF10 is a trans-factor required specifically for the C to U editing of site nad2-842. The MEF10 protein is characterized by a stretch of pentatricopeptide repeats (PPR) and a C-terminal extension domain ending with the amino acids DYW. Editing is lost in mutant plants but is recovered by transgenic introduction of an intact MEF10 gene. The MEF10 protein interacts with multiple organellar RNA editing factor 8 (MORF8) but not with other mitochondrial MORF proteins in yeast two hybrid assays. These results support the model that specific combinations of MORF and MEF proteins are involved in RNA editing in plant mitochondria. 相似文献