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首页> 外文期刊>Plant molecular biology reporter >Characterization and Expression of a Phytochelatin Synthase Gene in Birch-leaf Pear (Pyrus betulaefolia Bunge)
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Characterization and Expression of a Phytochelatin Synthase Gene in Birch-leaf Pear (Pyrus betulaefolia Bunge)

机译:桦叶梨(Pyrus betulaefolia Bunge)中植物螯合素合酶基因的表征和表达

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摘要

Phytochelatins play a major role in metal detoxification in plants. However, the molecular mechanisms of heavy metal detoxification remain unknown, and birch-leaf pear genes related to metal detoxification have not yet been identified. Here, we report the isolation of cDNA and genomic DNA sequences encoding a phytochelatin synthase (PCS) from birch-leaf pear (Pyrus betulaefolia Bunge). The PbPCS1 cDNA sequence contained 1,965 nucleotides of a 1,494 bp open reading frame (ORF), which encodes a 497-amino-acid protein with a molecular weight of 55.00 kDa. Its corresponding genomic DNA sequence consists of 3,820 nucleotides and eight exons separated by seven introns. The deduced amino acid sequence of PbPCS1 contains five Cys residues (56, 90, 91, 109 and 113 amino acids) that are highly conserved in the plant PCS1 family, and 12 cysteine residues putatively involved in heavy metal binding sites, which included three adjacent Cys–Cys components (331–332, 351–352 and 369–370 amino acids) in the C-terminal variable domain. Homology analysis of the deduced PbPCS1 amino acid sequence revealed that it shares a high sequence similarity amongst N-terminal amino acids and low similarity with C-terminal amino acids with plant PCS1 proteins deposited with NCBI. PbPCS1 was most related to PCS1 from legume plants Lotus japonicus (GenBank accession no. AAT80342) and soybean (Glycine max L.; AAL78384) as they were clustered into the same clade in a neighbor-joining phylogenetic tree. Quantitative real-time PCR (qPCR) expression analysis revealed that PbPCS1 had a very low basal expression level in untreated whole seedlings, and levels were higher in roots than in leaves and stems. After 24 h of exposure to 20 μM CdSO4, CuSO4 or ZnSO4, PbPCS1 expression increased significantly in different organs. In addition, L-buthionine-sulfo-ximine (BSO) can inhibit PbPCS1 expression in roots, stems and leaves, while L-glutathionereduced (GSH) stimulates PbPCS1 expression in different organs of birch-leaf pear.
机译:植物螯合素在植物的金属排毒中起主要作用。然而,重金属排毒的分子机制仍然未知,与金属排毒有关的白桦梨基因尚未被鉴定。在这里,我们报告从白桦叶梨(Pyrus betulaefolia Bunge)编码植物螯合素合酶(PCS)的cDNA和基因组DNA序列的分离。 PbPCS1 cDNA序列包含一个1,494 bp开放阅读框(ORF)的1,965个核苷酸,它编码一个分子量为55.00 kDa的497个氨基酸的蛋白质。其相应的基因组DNA序列由3,820个核苷酸和由七个内含子分隔的八个外显子组成。推导的PbPCS1氨基酸序列包含植物PCS1家族中高度保守的5个Cys残基(56、90、91、109和113个氨基酸),和12个半胱氨酸残基被推定参与重金属结合位点,其中包括三个相邻的C端可变域中的Cys-Cys成分(331-332、351-352和369-370个氨基酸)。推导的PbPCS1氨基酸序列的同源性分析表明,与NCBI保藏的植物PCS1蛋白相比,它在N端氨基酸之间具有很高的序列相似性,而在C端氨基酸之间却具有较低的相似性。 PbPCS1与豆科植物日本莲花(GenBank登录号AAT80342)和大豆(Glycine max L .; AAL78384)的PCS1最为相关,因为它们被聚集成到相邻连接的系统发育树中的同一进化枝中。实时定量PCR(qPCR)表达分析表明,PbPCS1在未经处理的整株幼苗中具有非常低的基础表达水平,并且根中的水平高于叶和茎中的水平。暴露于20μMCdSO4,CuSO4或ZnSO4 24小时后,不同器官中PbPCS1的表达显着增加。此外,L-丁硫氨酸-磺胺(BSO)可以抑制根,茎和叶中PbPCS1的表达,而L-谷胱甘肽受精(GSH)刺激白桦梨不同器官中的PbPCS1表达。

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