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Transformation of PRT6 RNAi construct into tomato (Solanum lycopersicum) cv. Micro-Tom

机译:PRT6 RNAI构建体转化为番茄(Solanum Lycopersicum)CV。微米

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PROTEOLYSIS 6 plays major role in the N-end rule pathway as N-recognin which functions as E3 ligase enzyme. It mediates ubiquitin processes that lead to degradation of unstable substrate protein. The aim of the current study is to transform the PRT6 gene into tomato (Solanum lycopersicum) from the cultivar Micro-Tom and to investigate its function in regulating ripening in tomato fruits. The PRT6_RNAi construct was successfully transformed into Agrobacterium C58 via heat shock method and transformed into seven days old cotyledon explants. Factors affecting transformation efficiency such as co-cultivation time and type of plant growth regulator combination were evaluated. Results from this study found that pre-cultured cotyledons from seven days old seedlings incubated for 2 days in co-cultivation medium increased shoot regeneration. Plant growth hormones zeatin combine with auxin produced a higher number of callus formation but lower shoot proliferation and transformation frequency compared to treatments of single plant hormone in the selection medium. Polymerase chain reaction (PCR) was performed on the regenerated shoots to confirm the integration of PRT6 fragment into the genome of transgenic plants. Based on PCR analysis, all putative shoots were positive transformants.
机译:蛋白水解6在N-END规则途径中发挥重要作用,作为幂蛋白,其用作E3连接酶。它介导泛素的方法,导致不稳定的底物蛋白的降解。目前研究的目的是将PRT6基因转化为来自品种微汤的番茄(Solanum Lycopersicum),并研究其在番茄水果中的调节成熟的功能。 PRT6_RNAI构建体通过热休克方法成功转化为C58,并转化为七天的子叶外植体。评估了影响转化效率的因素,如共培养时间和植物生长调节剂组合的类型。本研究结果发现,从七天的幼苗中培养预培养的子叶在共培养培养基中孵育2天,增加芽再生。植物生长激素Zeepin与养肝产生的结合产生了更高数量的愈伤组织形成,但与选择培养基中的单株植物激素治疗相比,脱枝增殖和转化频率降低。在再生芽上进行聚合酶链反应(PCR),以确认PRT6片段的整合到转基因植物的基因组中。基于PCR分析,所有推定的芽是阳性转化体。

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