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小核仁1编码一种五肽重复蛋白,该蛋白是玉米(Zea mays)和水稻(Oryza sativa)线粒体nad7转录本编辑和种子发育所必需的。

Small kernel 1 encodes a pentatricopeptide repeat protein required for mitochondrial nad7 transcript editing and seed development in maize (Zea mays) and rice (Oryza sativa).

作者信息

Li Xiao-Jie, Zhang Ya-Feng, Hou Mingming, Sun Feng, Shen Yun, Xiu Zhi-Hui, Wang Xiaomin, Chen Zong-Liang, Sun Samuel S M, Small Ian, Tan Bao-Cai

机构信息

School of Life Sciences, Tsinghua University, Beijing, 100084, China; Shenzhen Key Laboratory of Super Hybrid Rice Research, Division of Life & Health Sciences, Graduate School at Shenzhen, Tsinghua University, Shenzhen, 518055, China; State Key Lab of Agrobiotechnology, Institute of Plant Molecular Biology and Agrobiotechnology, School of Life Sciences, The Chinese University of Hong Kong, Shatin, N.T, Hong Kong.

出版信息

Plant J. 2014 Sep;79(5):797-809. doi: 10.1111/tpj.12584. Epub 2014 Jul 28.

Abstract

RNA editing modifies cytidines (C) to uridines (U) at specific sites in the transcripts of mitochondria and plastids, altering the amino acid specified by the DNA sequence. Here we report the identification of a critical editing factor of mitochondrial nad7 transcript via molecular characterization of a small kernel 1 (smk1) mutant in Zea mays (maize). Mutations in Smk1 arrest both the embryo and endosperm development. Cloning of Smk1 indicates that it encodes an E-subclass pentatricopeptide repeat (PPR) protein that is targeted to mitochondria. Loss of SMK1 function abolishes the C → U editing at the nad7-836 site, leading to the retention of a proline codon that is edited to encode leucine in the wild type. The smk1 mutant showed dramatically reduced complex-I assembly and NADH dehydrogenase activity, and abnormal biogenesis of the mitochondria. Analysis of the ortholog in Oryza sativa (rice) reveals that rice SMK1 has a conserved function in C → U editing of the mitochondrial nad7-836 site. T-DNA knock-out mutants showed abnormal embryo and endosperm development, resulting in embryo or seedling lethality. The leucine at NAD7-279 is highly conserved from bacteria to flowering plants, and analysis of genome sequences from many plants revealed a molecular coevolution between the requirement for C → U editing at this site and the existence of an SMK1 homolog. These results demonstrate that Smk1 encodes a PPR-E protein that is required for nad7-836 editing, and this editing is critical to NAD7 function in complex-I assembly in mitochondria, and hence to embryo and endosperm development in maize and rice.

摘要

RNA编辑可将线粒体和质体转录本特定位点的胞嘧啶(C)修饰为尿嘧啶(U),从而改变DNA序列所指定的氨基酸。在此,我们通过对玉米(Zea mays)小籽粒1(smk1)突变体进行分子特征分析,报告了线粒体nad7转录本关键编辑因子的鉴定结果。Smk1突变会阻止胚胎和胚乳发育。Smk1的克隆表明它编码一种靶向线粒体的E亚类五肽重复(PPR)蛋白。SMK1功能缺失消除了nad7 - 836位点的C→U编辑,导致脯氨酸密码子保留,而在野生型中该密码子经编辑后编码亮氨酸。smk1突变体的复合体I组装和NADH脱氢酶活性显著降低,线粒体生物发生异常。对水稻(Oryza sativa)同源物的分析表明,水稻SMK1在mitochondrial nad7 - 836位点的C→U编辑中具有保守功能。T-DNA敲除突变体表现出胚胎和胚乳发育异常,导致胚胎或幼苗致死。从细菌到开花植物,NAD7 - 279处的亮氨酸高度保守,对多种植物基因组序列的分析揭示了该位点C→U编辑需求与SMK1同源物存在之间的分子协同进化。这些结果表明,Smk1编码一种nad7 - 836编辑所需的PPR - E蛋白,这种编辑对于线粒体复合体I组装中的NAD7功能至关重要,因此对玉米和水稻的胚胎及胚乳发育也至关重要。

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