Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur 176061, HP, India.
Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur 176061, HP, India
J Exp Bot. 2015 Jul;66(13):3907-16. doi: 10.1093/jxb/erv198. Epub 2015 May 7.
This paper documents the engineering of Arabidopsis thaliana for the ectopic over-expression of SrKA13H (ent-kaurenoic acid-13 hydroxylase) cDNA from Stevia rebaudiana. HPLC analysis revealed the significant accumulation of steviol (1-3 μg g(-1) DW) in two independent transgenic Arabidopsis lines over-expressing SrKA13H compared with the control. Independent of the steviol concentrations detected, both transgenic lines showed similar reductions in endogenous bioactive gibberellins (GA1 and GA4). They possessed phenotypic similarity to gibberellin-deficient mutants. The reduction in endogenous gibberellin content was found to be responsible for dwarfism in the transgenics. The exogenous application of GA3 could rescue the transgenics from dwarfism. The hypocotyl, rosette area, and stem length were all considerably reduced in the transgenics. A noteworthy decrease in pollen viability was noticed and, similarly, a retardation of 60-80% in pollen germination rate was observed. The exogenous application of steviol (0.2, 0.5, and 1.0 μg ml(-1)) did not influence pollen germination efficiency. This has suggested that in planta formation of steviol was not responsible for the observed changes in transgenic Arabidopsis. Further, the seed yield of the transgenics was reduced by 24-48%. Hence, this study reports for the first time that over-expression of SrKA13H cDNA in Arabidopsis has diverted the gibberellin biosynthetic route towards steviol biosynthesis. The Arabidopsis transgenics showed a significant reduction in endogenous gibberellins that might be responsible for the dwarfism, and the abnormal behaviour of pollen germination and seed set.
本文记录了拟南芥中亚麻酸 13-羟化酶(ent-贝壳杉烯酸-13-羟化酶) cDNA 的异位过表达工程,该 cDNA 来自甜叶菊(Stevia rebaudiana)。HPLC 分析显示,与对照相比,过表达 SrKA13H 的两个独立的转基因拟南芥系中显著积累了甜菊醇(1-3 μg g(-1) DW)。独立于检测到的甜菊醇浓度,两个转基因系均表现出内源生物活性赤霉素(GA1 和 GA4)的类似减少。它们表现出与赤霉素缺陷突变体相似的表型。发现内源赤霉素含量的减少是转基因矮化的原因。外源 GA3 的应用可以使转基因系从矮化中恢复。转基因系的下胚轴、莲座叶面积和茎长均显著减少。注意到花粉活力明显下降,同样观察到花粉萌发率降低 60-80%。外源甜菊醇(0.2、0.5 和 1.0 μg ml(-1))的应用并未影响花粉萌发效率。这表明植物体内甜菊醇的形成不是导致转基因拟南芥观察到的变化的原因。此外,转基因系的种子产量减少了 24-48%。因此,本研究首次报道,SrKA13H cDNA 在拟南芥中的过表达使赤霉素生物合成途径转向甜菊醇生物合成。转基因拟南芥内源赤霉素显著减少,这可能是导致矮化以及花粉萌发和结实异常的原因。