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首页> 外文期刊>The New Phytologist >GhZFP1, a novel CCCH-type zinc finger protein from cotton, enhances salt stress tolerance and fungal disease resistance in transgenic tobacco by interacting with GZIRD21A and GZIPR5
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GhZFP1, a novel CCCH-type zinc finger protein from cotton, enhances salt stress tolerance and fungal disease resistance in transgenic tobacco by interacting with GZIRD21A and GZIPR5

机译:GhZFP1是一种新型的棉花CCCH型锌指蛋白,通过与GZIRD21A和GZIPR5相互作用增强转基因烟草的耐盐胁迫性和抗真菌病性

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摘要

Zinc finger proteins are a superfamily involved in many aspects of plant growth and development. However, CCCH-type zinc finger proteins involved in plant stress tolerance are poorly understood. A cDNA clone designated Gossypium hirsutum zinc finger protein 1 (GhZFP1), which encodes a novel CCCH-type zinc finger protein, was isolated from a salt-induced cotton (G. hirsutum) cDNA library using differential hybridization screening and further studied in transgenic tobacco Nicotiana tabacum cv. NC89. Using yeast two-hybrid screening (Y2H), proteins GZIRD21A (GhZFP1 interacting and responsive to dehydration protein 21A) and GZIPR5 (GhZFP1 interacting and pathogenesis-related protein 5), which interacted with GhZFP1, were isolated. GhZFP1 contains two typical zinc finger motifs (Cx8Cx5Cx3H and Cx5Cx4Cx3H), a putative nuclear export sequence (NES) and a potential nuclear localization signal (NLS). Transient expression analysis using a GhZFP1::GFP fusion gene in onion epidermal cells indicated a nuclear localization for GhZFP1. RNA blot analysis showed that the GhZFP1 transcript was induced by salt (NaCl), drought and salicylic acid (SA). The regions in GhZFP1 that interact with GZIRD21A and GZIPR5 were identified using truncation mutations. Overexpression of GhZFP1 in transgenic tobacco enhanced tolerance to salt stress and resistance to Rhizoctonia solani. Therefore, it appears that GhZFP1 might be involved as an important regulator in plant responses to abiotic and biotic stresses.
机译:锌指蛋白是涉及植物生长和发育的许多方面的超家族。但是,人们对与植物抗逆性有关的CCCH型锌指蛋白知之甚少。使用差异杂交筛选从盐诱导棉花(G. hirsutum)cDNA文库中分离出一种编码Gossypium hirsutum锌指蛋白1(GhZFP1)的cDNA克隆,该cDNA编码采用新型CCCH型锌指蛋白,并在转基因烟草中进行了进一步研究烟草NC89。使用酵母双杂交筛选(Y2H),分离了与GhZFP1相互作用的蛋白GZIRD21A(与脱水蛋白21A相互作用并对其产生响应)和GZIPR5(与GhZFP1相互作用且与发病机理相关的蛋白5)。 GhZFP1包含两个典型的锌指基序(Cx8Cx5Cx3H和Cx5Cx4Cx3H),推定的核输出序列(NES)和潜在的核定位信号(NLS)。在洋葱表皮细胞中使用GhZFP1 :: GFP融合基因进行的瞬时表达分析表明,GhZFP1的核定位。 RNA印迹分析表明,GhZFP1转录本是由盐(NaCl),干旱和水杨酸(SA)诱导的。 GhZFP1中与GZIRD21A和GZIPR5相互作用的区域是使用截断突变鉴定的。 GhZFP1在转基因烟草中的过表达增强了对盐胁迫的耐受性和对茄红枯菌的抗性。因此,似乎GhZFP1可能是植物对非生物和生物胁迫的重要调控因子。

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