HIGH FREQUENCY GENETIC TRANSFORMATION OF CICHORIUM INTYBUS L. USING nptII GENE AS A SELECTIVE MARKER.

TSitologiia i genetika Pub Date : 2015-07-01
N Matvieieva, A Shakhovsky, O Kvasko, N Kuchuk
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Abstract

Cichorium intybus L. is an important vegetable crop used as salad (leaf form) and for the production of coffee substitutes (root form). At the same time these plants can also be used in biotechnologies for synthesis of pharmaceutical proteins. Here we report the possibility of high frequency Agrobacterium rhizogenes- or A. tumefaciens-mediated transformation of C. intybus L. for construction of transgenic "hairy" roots and plants. The used plasmids contained target human interferonifn-α2b gene, Mycobacterium tuberculosis ESAT6:Ag85B antigene esxA::fbpB(ΔTMD) fused gene and human telomerase reverse transcriptase h Tert gene. Using of nptII gene as a selective one was preferable to the bar gene for chicory. In this case the frequency of transgenic plants or "hairy" roots formation was significantly higher. Cultivation of explants on the medium with Basta in concentration 1-2 mg/l have led to plants death or to significant reduction of number of shoots formed. Frequency of "hairy" roots formation varied from 5.9 to 42.3% after A. rhizogenes-mediated transformation. Frequency of regeneration of transgenic plants varied from 10 to 86% after A. tumefaciens-mediated transformation. Both A. rhizogenes- and A. tumefaciens-mediated transformation frequency depended on the type of explants, roots or cotyledons, and vector used. Usage of A. tumefaciens carrying pCB064 plasmid (target esxA:fbpB(ΔTMD) fused gene and nptII selective gene) resulted in the most effective regeneration of transgenic plants with regeneration frequency up to 86%. In the case of chicory A. rhizogenes-mediated transformation the highest regeneration frequency up to 42.3% was demonstrated using p CB161 vector with ifn-α2b target gene and nptII selective gene.

利用 nptII 基因作为选择性标记,实现茵陈的高频基因转化。
Cichorium intybus L. 是一种重要的蔬菜作物,可用作沙拉(叶片)和生产咖啡替代品(根茎)。同时,这些植物也可用于合成药物蛋白质的生物技术中。在此,我们报告了根瘤农杆菌或瘤单胞菌介导的高频转化 C. intybus L. 的可能性,以构建转基因 "多毛 "根和植物。所使用的质粒含有目标人类干扰素-α2b 基因、结核分枝杆菌 ESAT6:Ag85B 抗原 esxA::fbpB(ΔTMD) 融合基因和人类端粒酶逆转录酶 h Tert 基因。对菊苣来说,使用 nptII 基因作为选择基因比使用 bar 基因更好。在这种情况下,转基因植株或 "毛 "根形成的频率明显更高。在浓度为 1-2 毫克/升的巴斯塔培养基上培养外植体会导致植株死亡或形成的芽数量明显减少。在根瘤菌介导的转化过程中,"毛 "根形成的频率从 5.9% 到 42.3% 不等。在 A. tumefaciens 介导的转化过程中,转基因植株的再生率从 10% 到 86% 不等。根瘤菌和瘤杆菌介导的转化频率取决于外植体(根或子叶)的类型和使用的载体。使用携带 pCB064 质粒(目标 esxA:fbpB(ΔTMD) 融合基因和 nptII 选择基因)的 A. tumefaciens 能最有效地再生转基因植株,再生频率高达 86%。在菊苣根瘤菌介导的转化中,使用带有 ifn-α2b 目标基因和 nptII 选择基因的 p CB161 载体的再生率最高,达到 42.3%。
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