2022
DOI: 10.1093/plcell/koac082
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A mitochondrial RNA processing protein mediates plant immunity to a broad spectrum of pathogens by modulating the mitochondrial oxidative burst

Abstract: Mitochondrial function depends on the RNA processing of mitochondrial gene transcripts by nucleus-encoded proteins. This post-transcriptional processing involves the large group of nuclear-encoded pentatricopeptide repeat (PPR) proteins. Mitochondrial processes represent a crucial part in animal immunity, but whether mitochondria play similar roles in plants remains unclear. Here, we report the identification of RESISTANCE TO PHYTOPHTHORA PARASITICA 7 (AtRTP7), a P-type PPR protein, in Arabidopsis thaliana and… Show more

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Cited by 23 publications
(8 citation statements)
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“…PPR proteins have been demonstrated to be a regulator of resistance to pathogen infection in plants [2]. AtRTP7, a P-type PPR protein, mediates plant immunity to a broad spectrum of pathogens by modulating the mitochondrial oxidative burst in Arabidopsis [49]. OsNBL3, a rice mitochondrion-localized PPR protein, regulated enhanced resistance to the fungal and bacterial pathogens [24].…”
Section: Discussionmentioning
confidence: 99%
“…PPR proteins have been demonstrated to be a regulator of resistance to pathogen infection in plants [2]. AtRTP7, a P-type PPR protein, mediates plant immunity to a broad spectrum of pathogens by modulating the mitochondrial oxidative burst in Arabidopsis [49]. OsNBL3, a rice mitochondrion-localized PPR protein, regulated enhanced resistance to the fungal and bacterial pathogens [24].…”
Section: Discussionmentioning
confidence: 99%
“…P‐type PPR proteins are often involved in RNA splicing of mitochondrial group II introns, 5′ end processing, and translation (Manavski et al ., 2012 ; Wang et al ., 2021 ; Yang et al ., 2022c ; Zhang et al ., 2017 ). The restorer gene ZmRf5 identified in this study encodes a canonical P‐type PPR protein without direct contacting with atp6c (Figure S3 ).…”
Section: Discussionmentioning
confidence: 99%
“…After the control GFP was removed, the remaining proteins were the candidate target proteins. For CM-H2DCFDA staining assay, TRV-GFP and TRV-NbRBP3 silenced plants treated with 10 μM flg22 for 0.5 h were stained with 10 μM CM-H 2 DCFDA for 0.5-1 h to detect ROS, then washed twice before imaging (Yang et al, 2022). CM-H 2 DCFDA was excited at 488 nm with emission collected at 500-540 nm.…”
Section: Co-immunoprecipitationmentioning
confidence: 99%