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首页> 外文期刊>Journal of the Japanese Society for Horticultural Science >Virus-induced gene silencing in apricot (Prunus armeniaca L.) and Japanese apricot (P. mume Siebold & Zucc.) with the apple latent spherical virus vector system.
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Virus-induced gene silencing in apricot (Prunus armeniaca L.) and Japanese apricot (P. mume Siebold & Zucc.) with the apple latent spherical virus vector system.

机译:苹果潜伏球形病毒载体系统在杏(Prunus armeniaca L.)和日本杏(P. mume Siebold&Zucc。)中病毒诱导的基因沉默。

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摘要

Apple latent spherical virus (ALSV) vectors have been shown to effectively induce stable virus-induced gene silencing (VIGS) in a wide range of plant species, including rosaceous fruit tree species such as apple (Malus x domestica Borkh.), pear (Pyrus communis L.), and Japanese pear (P. pyrifolia Nakai). In this study, we attempted to develop a VIGS-based gene evaluation system for two Prunus fruit tree species, apricot and Japanese apricot, using ALSV vectors. A partial sequence of the P. armeniaca PHYTOENE DESATURASE (ParPDS) gene was cloned and ligated into the T-DNA region of a binary vector, pBICAL2, designed based on RNA2 of ALSV. The resultant pBICAL2-ParPDS was introduced into a disarmed Agrobacterium strain. EHA105. pBICAL1, a binary plasmid for the expression of ALSV RNA1 in plants, was also introduced into EHA105. Leaves of Nicotiana benthamiana were infected with pBICAL1/EHA105 and pBICAL2-ParPDS/EHA105 simultaneously to produce and amplify recombinant ALSV particles. The amplified ParPDS-ALSV in N. benthamiana was isolated and infected into the cotyledons of apricot and Japanese apricot seedlings by particle bombardment. Although our attempts to infect wild and recombinant ALSVs into Japanese apricot seedlings were unsuccessful, uniform discoloration of the upper leaves, a typical phenotype of PDS knock down, was observed several weeks after inoculation in apricot seedlings. We discuss the possible use of this VIGS-based gene evaluation system in Prunus.
机译:苹果潜伏球形病毒(ALSV)载体已显示可在多种植物物种中有效诱导稳定的病毒诱导基因沉默(VIGS),包括苹果(Malus x domestica Borkh。),梨(Pyrus)等蔷薇果树种。 communis L.)和日本梨(P. pyrifolia Nakai)。在这项研究中,我们试图使用ALSV载体为两个李子杏树和日本杏树开发基于VIGS的基因评估系统。克隆了Armeniaca PHYTOENE DESATURASE(ParPDS)基因的部分序列,并将其连接到基于ALSV RNA2设计的二元载体pBICAL2的T-DNA区中。将所得的pBICAL2-ParPDS引入解除武装的农杆菌菌株中。 EHA105。 pBICAL1,一种用于在植物中表达ALSV RNA1的二元质粒,也被引入到EHA105中。同时用pBICAL1 / EHA105和pBICAL2-ParPDS / EHA105感染本氏烟草的叶片,以产生和扩增重组ALSV颗粒。分离出在本氏烟草中扩增的ParPDS-ALSV,并通过粒子轰击将其感染到杏和日本杏幼苗的子叶中。尽管我们尝试将野生和重组ALSV感染到日本杏树苗中的尝试均未成功,但在杏树苗中接种数周后,观察到上部叶片的均匀变色(PDS的典型表型被击倒)。我们讨论了在李属中这种基于VIGS的基因评估系统的可能用途。

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