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The rice PPR756 coordinates with MORFs for multiple RNA editing in mitochondria

biorxiv. 2019; 
Qiannan Zhang, View Yanghong Xu, Jishuai Huang, Kai Zhang, Haijun Xiao, Xiaojian Qin, Linlin Zhu, Yingguo Zhu, Jun Hu
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Recombinant Proteins The recombinant protein was created with a fusion of MBP in the PPR75641-756 517 518 N-terminus and 6 x His in the C-terminus which was purified across two columns author/funder. It is made available under a CC-BY-NC-ND 4.0 International license. bioRxiv preprint doi: https://doi.org/10.1101/844241. The copyright holder for this preprint (which was not peer-reviewed) is the 26 equipped with Ni2+ 519 affinity resin (Ni-NTA Resin, GenScript) and MBP (PurKine 520 MBP-Tag Dextrin Resin 6FF, Abbkine) in turn as well as another control fusion 521 protein containing only MBP and His tags. Get A Quote

摘要

In land plants, the pentatricopeptide repeat (PPR) proteins form a large family accounting for post-transcriptional process in mitochondria and chloroplasts. Although studies showed a number of PPR proteins generally influence the editing of organellar genes acting as a member of editing complex, few of them were characterized detailed in rice. Here, we reported a PLS-E subclass PPR protein in rice, PPR756, loss function of which lead to the abolishment of RNA editing events among three sites in mitochondrial genes including atp6 (ATP synthase F0 subunit 6), ccmC (cytochrome c biogenesis C) and nad7 (NADH dehydrogenase subunit 7). The defective C-to-U transformation of atp6-368, ccmC-236 and nad7-83 resulted in... More

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