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Cloning of a new glutathione peroxidase gene from tea plant (Camellia sinensis) and expression analysis under biotic and abiotic stresses

机译:茶树(Camellia sinensis)谷胱甘肽过氧化物酶新基因的克隆及其在生物和非生物胁迫下的表达分析

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Background Tea plant, Camellia sinensis (L.) O. Kuntze, a well-known heavy metal hyperaccumulator, possesses a powerful tolerance to heavy metals. The heavy metal stresses lead to reactive oxygen species (ROS) production, and high concentration of ROS is harmful to plants. The glutathione peroxidase gene has positive function to damage induced by ROS. To understand the mechanism of tolerance to deferent stresses in tea plant, a new glutathione peroxidase gene of tea plant was cloned and its expression pattern was analyzed under abiotic and biotic stresses. Results A novel cDNA encoding glutathione peroxidase of tea plant (Camellia sinensis) was isolated by rapid amplification of cDNA ends (RACE) method and designated as CsGPX2 (GenBank Accession No. JQ247186). This full-length sequence was 917 nucleotides including a 510 bp open reading frame (ORF), which encoded a polypeptide of 169 amino acids. The deduced amino acid sequence showed high homology with glutathione peroxidases of angiosperms and contained the characteristic conserved motifs of ILAFPCNQF and FTVKD, the highest level of similarity was 85% to a glutathione peroxidase from Ricinus communis (Accession NO. XP_002509790.1). Tissue expression pattern analysis indicated that CsGPX2 expressed similarly in root, stem, leaf and flower of tea plant. The CsGPX2 gene showed strong responses to most abiotic stresses including salinity, heavy metal toxicity, drought, heat, plant hormones, but could not be induced by biotic treatment. Conclusions The result suggested that CsGPX2 had potential function in protecting tea plant from peroxidative damage induced by some abiotic stresses.
机译:背景技术茶树-山茶(L.)O。Kuntze,一种众所周知的重金属超蓄积剂,对重金属具有强大的耐受力。重金属胁迫导致产生活性氧(ROS),并且高浓度的ROS对植物有害。谷胱甘肽过氧化物酶基因对由ROS引起的损伤具有正功能。为了了解茶树对不同胁迫的耐受机制,克隆了一个新的茶树谷胱甘肽过氧化物酶基因,并分析了其在非生物和生物胁迫下的表达模式。结果通过快速扩增cDNA末端(RACE)方法分离到编码茶树(Camellia sinensis)谷胱甘肽过氧化物酶的新cDNA,命名为CsGPX2(GenBank登录号JQ247186)。该全长序列为917个核苷酸,其中包括一个510 bp的开放阅读框(ORF),其编码169个氨基酸的多肽。推导的氨基酸序列与被子植物的谷胱甘肽过氧化物酶具有高度的同源性,并具有ILAFPCNQF和FTVKD的保守性特征基序,与来自蓖麻的谷胱甘肽过氧化物酶的最高相似度为85%(登录号XP_002509790.1)。组织表达模式分析表明,CsGPX2在茶树的根,茎,叶和花中表达相似。 CsGPX2基因显示出对大多数非生物胁迫的强烈反应,包括盐度,重金属毒性,干旱,高温,植物激素,但不能通过生物处理诱导。结论结果表明,CsGPX2具有保护茶树免受非生物胁迫引起的过氧化损伤的潜在功能。

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