Tetrapyrrole biosynthesis pathway regulates plastid-to-nucleus signaling by controlling plastid gene expression in plants

文献类型: 外文期刊

第一作者: Wang, Yunlong

作者: Wang, Yunlong;Wang, Yihua;Zhu, Xiaopin;Dong, Hui;Duan, Erchao;Teng, Xuan;Zhao, Huanhuan;Chen, Rongbo;Chen, Xiaoli;Lei, Jie;Yang, Hang;Tian, Yunlu;Chen, Liangming;Liu, Xi;Liu, Shijia;Jiang, Ling;Wan, Jianmin;Ren, Yulong;Wang, Haiyang;Wan, Jianmin

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关键词: tetrapyrrole biosynthesis; plastid gene expression; plastid retrograde signal

期刊名称:PLANT COMMUNICATIONS ( 影响因子:10.5; 五年影响因子:10.5 )

ISSN: 2590-3462

年卷期: 2023 年 4 卷 1 期

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收录情况: SCI

摘要: Plastid-to-nucleus retrograde signaling coordinates nuclear gene expression with chloroplast developmental status and is essential for the photoautotrophic lifestyle of plants. Previous studies have established that tetrapyrrole biosynthesis (TPB) and plastid gene expression (PGE) play essential roles in plastid retrograde signaling during early chloroplast biogenesis; however, their functional relationship remains unknown. In this study, we generated a series of rice TPB-related gun (genome uncoupled) mutants and systematically analyzed their effects on nuclear and plastid gene expression under normal conditions or when subjected to treatments with norflurazon (NF; a noncompetitive inhibitor of carotenoid biosynthesis) and/or lincomycin (Lin; a specific inhibitor of plastid translation). We show that under NF treatment, expression of plastid-encoded polymerase (PEP)-transcribed genes is significantly reduced in the wild type but is derepressed in the TPB-related gun mutants. We further demonstrate that the derepressed expression of PEPtranscribed genes may be caused by increased expression of the PEP core subunit and nuclear-encoded sigma factors and by elevated copy numbers of plastid genome per haploid genome. In addition, we show that expression of photosynthesis-associated nuclear genes (PhANGs) and PEP-transcribed genes is correlated in the rice TPB-related gun mutants, with or without NF or Lin treatment. A similar correlation between PhANGs and PGE is also observed in the Arabidopsis gun4 and gun5 mutants. Moreover, we show that increased expression of PEP-transcribed plastid genes is necessary for the gun phenotype in NF-treated TPB-related gun mutants. Further, we provide evidence that these TPB-related GUN genes act upstream of GUN1 in the regulation of retrograde signaling. Taken together, our results suggest that the TPB-related GUN genes control retrograde plastid signaling by regulating the PGE-dependent retrograde signaling pathway.

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