NPR1 Translocation from Chloroplast to Nucleus Activates Plant Tolerance to Salt Stress

被引:7
|
作者
Seo, Soyeon [1 ]
Kim, Yumi [1 ]
Park, Kyyoung [1 ]
机构
[1] Sunchon Natl Univ, Dept Biomed Sci, Sunchon 57922, Jeollanam Do, South Korea
基金
新加坡国家研究基金会;
关键词
stress tolerance; retrograde signaling; NPR1; transcription coactivator; chloroplast; redox; Nicotiana tabacum; SALICYLIC-ACID; BREFELDIN-A; BINDING; PROTEIN; BIOSYNTHESIS; WHIRLY1; GOLGI;
D O I
10.3390/antiox12051118
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
Chloroplasts play crucial roles in biotic and abiotic stress responses, regulated by nuclear gene expression through changes in the cellular redox state. Despite lacking the N-terminal chloroplast transit peptide (cTP), nonexpressor of pathogenesis-related genes 1 (NPR1), a redox-sensitive transcriptional coactivator was consistently found in the tobacco chloroplasts. Under salt stress and after exogenous application of H2O2 or aminocyclopropane-1-carboxylic acid, an ethylene precursor, transgenic tobacco plants expressing green fluorescent protein (GFP)-tagged NPR1 (NPR1-GFP) showed significant accumulation of monomeric nuclear NPR1, irrespective of the presence of cTP. Immunoblotting and fluorescence image analyses indicated that NPR1-GFP, with and without cTP, had similar molecular weights, suggesting that the chloroplast-targeted NPR1-GFP is likely translocated from the chloroplasts to the nucleus after processing in the stroma. Translation in the chloroplast is essential for nuclear NPR1 accumulation and stress-related expression of nuclear genes. An overexpression of chloroplast-targeted NPR1 enhanced stress tolerance and photosynthetic capacity. In addition, compared to the wild-type lines, several genes encoding retrograde signaling-related proteins were severely impaired in the Arabidopsis npr1-1 mutant, but were enhanced in NPR1 overexpression (NPR1-Ox) transgenic tobacco line. Taken together, chloroplast NPR1 acts as a retrograding signal that enhances the adaptability of plants to adverse environments.
引用
收藏
页数:23
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