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Dek570-1是一种PPR-DYW蛋白,通过调节线粒体和叶绿体中的C到U RNA编辑,对玉米种子和植株发育至关重要。

Dek570-1, a PPR-DYW protein, is required for maize seed and plant development via modulation of C-to-U RNA editing in mitochondria and chloroplasts.

作者信息

Li Wenjie, Zhao Mengsha, Liu Baiyu, Liu Yecan, Deng Jiaying, Gu Yu, Liu Min, Cheng Wen, Ding Zhaohua, Li Kunpeng

机构信息

The Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, Qingdao, 266237, China.

Maize Institute of Shandong Academy of Agricultural Sciences, Jinan, 250100, China.

出版信息

Planta. 2025 Feb 22;261(4):64. doi: 10.1007/s00425-025-04634-z.

Abstract

Maize Dek570-1 affects the expression and function of organellar genes by performing cytidines-to-uridines RNA editing at specific sites of mitochondrial and chloroplast transcripts, thereby regulating seed and plant development. Cytidines-to-uridines (C-to-U) RNA editing at specific sites of mitochondrial and plastid transcripts is crucial for the expression and function of organellar genes, which requires PPR proteins. Here, we report the map-based cloning and characterization of Defective Kernel 570-1 (Dek570-1), which encodes a PPR-DYW protein and is an allele of Emp17. However, compared to the empty pericarp and embryonic lethality of emp17 (W22 background), dek570-1 (Zheng58 background) can produce small but viable seeds despite reducing the size of embryo and endosperm. dek570-1 plants are short and yellowed, but they can reproduce offspring. In mitochondria, loss-of-function of Dek570-1 abolishes the C-to-U editing at nad2-677 and ccmF-799 sites, and reduces the editing at ccmF-906 site, consistent with Emp17 deficiency. But unlike the reduced editing of the ccmF-966 site in emp17, the ccmF-966 site in dek570-1 is fully edited, and several other editing sites such as ccmF-87, ccmF-301, and ccmF-306 are also found. More noteworthy is that Dek570-1 is not only located in mitochondria like Emp17, but also in chloroplasts. Correspondingly, the editing at rpl20-308 site of dek570-1 chloroplasts was significantly reduced, affecting the expression of some rRNAs, plastid-encoded RNA polymerase (PEP)- and nuclear-encoded single-subunit RNA polymerase (NEP)-dependent genes, thereby reducing chlorophyll accumulation and photosynthetic rate. Together, these results indicate that Dek570-1 is essential for C-to-U editing at several sites in mitochondrial and chloroplast transcripts, as well as for seed and plant development, and that this locus (Zm00001d028422) may have generated some functional evolutionary divergence in maize with different genetic backgrounds.

摘要

玉米Dek570-1通过在线粒体和叶绿体转录本的特定位点进行胞嘧啶到尿嘧啶的RNA编辑,影响细胞器基因的表达和功能,从而调控种子和植株发育。线粒体和质体转录本特定位点的胞嘧啶到尿嘧啶(C-to-U)RNA编辑对于细胞器基因的表达和功能至关重要,这需要PPR蛋白。在此,我们报告了缺陷籽粒570-1(Dek570-1)的图位克隆和特征分析,它编码一个PPR-DYW蛋白,是Emp17的一个等位基因。然而,与emp17(W22背景)的空果皮和胚胎致死性相比,dek570-1(郑58背景)尽管减小了胚和胚乳的大小,但能产生小而有活力的种子。dek570-1植株矮小且发黄,但能繁殖后代。在线粒体中,Dek570-1功能丧失消除了nad2-677和ccmF-799位点的C-to-U编辑,并降低了ccmF-906位点的编辑,这与Emp17缺陷一致。但与emp17中ccmF-966位点编辑减少不同,dek570-1中的ccmF-966位点被完全编辑,并且还发现了其他几个编辑位点,如ccmF-87、ccmF-301和ccmF-306。更值得注意的是,Dek570-1不仅像Emp17一样定位于线粒体中,还定位于叶绿体中。相应地,dek570-1叶绿体rpl20-308位点的编辑显著减少,影响了一些rRNA、质体编码的RNA聚合酶(PEP)和核编码的单亚基RNA聚合酶(NEP)依赖性基因的表达,从而降低了叶绿素积累和光合速率。总之,这些结果表明Dek570-1对于线粒体和叶绿体转录本中几个位点的C-to-U编辑以及种子和植株发育至关重要,并且该基因座(Zm00001d028422)在具有不同遗传背景的玉米中可能产生了一些功能上的进化分歧。

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