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首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Expression analysis of MusaNAC68 transcription factor and its functional analysis by overexpression in transgenic banana plants
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Expression analysis of MusaNAC68 transcription factor and its functional analysis by overexpression in transgenic banana plants

机译:MusaNAC68转录因子在转基因香蕉植株中的表达分析及过表达的功能分析

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摘要

NAC (NAM, ATAF and CUC) proteins are plant-specific transcription factors regulating development and responses to stress. One of NAC proteins from banana is NAC68, and expression analysis indicated its positive association to stress conditions. The 5'-proximal region of MusaNAC68 was isolated and sequence analysis indicated presence of stress related cis-elements and cis-elements involved in auxin-signaling. Expression of MusaNAC68 was maximum in roots and positively correlated with application of alpha-naphthaleneacetic acid. Nuclear localization of MusaNAC68 was determined by fusion of green-fluorescent protein with MusaNAC68 and transiently overexpressing in banana embryogenic cells. Transgenic lines were marginally taller and displayed more abundant roots than control along with altered expression of auxin-responsive genes like auxin-responsive factors and IAA/Aux (indoleacetic acid-induced protein) genes. Transgenic plants overexpressing MusaNAC68 displayed higher activity of polyphenol oxidase and rapid browning of plant extract. Transgenic lines showed better tolerance to stress induced by NaCl and mannitol and produced more shoot biomass. Leaf disc assay showed that transgenic lines retain more chlorophyll and lower malondialdehyde than control under salinity and drought. Transgenic line constitutively overexpressing MusaNAC68 showed elevated expression of many stress-responsive genes indicating its involvement in salinity and drought tolerance in banana.
机译:NAC(NAM,ATAF和CUC)蛋白是植物特异性转录因子,可调节发育和对胁迫的反应。来自香蕉的NAC蛋白之一是NAC68,表达分析表明其与胁迫条件呈正相关。分离了MusaNAC68的5'-近端区域,序列分析表明存在与压力相关的顺式元素和生长素信号传导中涉及的顺式元素。 MusaNAC68的表达在根中最大,并且与α-萘乙酸的施用正相关。通过将绿色荧光蛋白与MusaNAC68融合并在香蕉胚发生细胞中瞬时过表达来确定MusaNAC68的核定位。转基因品系比对照略高,并且显示出比对照更丰富的根,以及生长素反应性基因如生长素反应性因子和IAA / Aux(吲哚乙酸诱导的蛋白质)基因的表达发生了变化。过表达MusaNAC68的转基因植物表现出较高的多酚氧化酶活性,并且植物提取物快速褐变。转基因品系显示出对NaCl和甘露醇诱导的胁迫更好的耐受性,并产生了更多的茎生物量。叶盘试验表明,在盐分和干旱条件下,转基因品系比对照品保留更多的叶绿素和较低的丙二醛。组成型过表达MusaNAC68的转基因品系显示许多胁迫响应基因的表达升高,表明其参与了香蕉的盐度和耐旱性。

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