首页> 外文期刊>Molecular Biology Reports >Cloning and characterization of a novel stress-responsive WRKY transcription factor gene (MusaWRKY71) from Musa spp. cv. Karibale Monthan (ABB group) using transformed banana cells
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Cloning and characterization of a novel stress-responsive WRKY transcription factor gene (MusaWRKY71) from Musa spp. cv. Karibale Monthan (ABB group) using transformed banana cells

机译:Musa spp胁迫应答WRKY转录因子新基因(MusaWRKY71)的克隆和鉴定。简历。 Karibale Monthan(ABB集团)使用转化的香蕉细胞

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WRKY transcription factor proteins play significant roles in plant stress responses. Here, we report the cloning and characterization of a novel WRKY gene, MusaWRKY71 isolated from an edible banana cultivar Musa spp. Karibale Monthan (ABB group). MusaWRKY71, initially identified using in silico approaches from an abiotic stress-related EST library, was later extended towards the 3′ end using rapid amplification of cDNA ends technique. The 1299-bp long cDNA of MusaWRKY71 encodes a protein with 280 amino acids and contains a characteristic WRKY domain in the C-terminal half. Although MusaWRKY71 shares good similarity with other monocot WRKY proteins the substantial size difference makes it a unique member of the WRKY family in higher plants. The 918-bp long 5′ proximal region determined using thermal asymmetric interlaced-polymerase chain reaction has many putative cis-acting elements and transcription factor binding motifs. Subcellular localization assay of MusaWRKY71 performed using a GFP-fusion platform confirmed its nuclear targeting in transformed banana suspension cells. Importantly, MusaWRKY71 expression in banana plantlets was up-regulated manifold by cold, dehydration, salt, ABA, H2O2, ethylene, salicylic acid and methyl jasmonate treatment indicating its involvement in response to a variety of stress conditions in banana. Further, transient overexpression of MusaWRKY71 in transformed banana cells led to the induction of several genes, homologues of which have been proven to be involved in diverse stress responses in other important plants. The present study is the first report on characterization of a banana stress-related transcription factor using transformed banana cells.
机译:WRKY转录因子蛋白在植物胁迫反应中起重要作用。在这里,我们报告克隆和表征的新型WRKY基因,从可食用的香蕉品种Musa spp分离得到的MusaWRKY71。 Karibale Monthan(ABB集团)。 MusaWRKY71最初是使用非生物胁迫相关EST文库的计算机方法鉴定的,后来使用cDNA末端快速扩增技术将其延伸至3'末端。 MusaWRKY71的1299 bp长cDNA编码具有280个氨基酸的蛋白质,并在C端一半处包含特征性WRKY结构域。尽管MusaWRKY71与其他单子叶植物WRKY蛋白具有良好的相似性,但其巨大的大小差异使其成为高等植物中WRKY家族的独特成员。使用热不对称交错聚合酶链反应确定的918 bp长5'近端区域具有许多假定的顺式作用元件和转录因子结合基序。使用GFP融合平台进行的MusaWRKY71的亚细胞定位分析证实了其在转化的香蕉悬浮细胞中的核靶向性。重要的是,通过低温,脱水,盐,ABA,H 2 O 2 ,乙烯,水杨酸和茉莉酸甲酯处理,香蕉幼苗中的MusaWRKY71表达被上调。参与应对香蕉中的各种胁迫条件。此外,在转化的香蕉细胞中MusaWRKY71的瞬时过表达导致了几个基因的诱导,已经证明了其同源物与其他重要植物中的多种胁迫反应有关。本研究是使用转化的香蕉细胞表征香蕉胁迫相关转录因子的第一份报告。

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