Tewari-Singh N, Sen J, Kiesecker H, Reddy V S, Jacobsen H-J, Guha-Mukherjee S
School of Life Sciences, Jawaharlal Nehru University, 110067 New Delhi, India.
Plant Cell Rep. 2004 Mar;22(8):576-83. doi: 10.1007/s00299-003-0730-6. Epub 2004 Jan 29.
A desensitized aspartate kinase (AK) gene has been developed as a non-antibiotic selection marker for use in the production of transgenic chickpea ( Cicer arietinum L.). Transgenic shoots regenerated from embryo explants bombarded with the desensitized AK gene were selected on media containing two amino acids, lysine and threonine (LT). Approximately 15% of the putative transgenic shoots of vars. P-362 and P-1042 survived after 4 weeks of growth on MSB5 medium (MS mineral salts and B5 vitamins) containing 2 microM thidiazuron (TDZ) and 2 mM lysine and 2 m M threonine. These shoots were subsequently grown on MSB5 medium supplemented with 2 micro M TDZ and 5 mM lysine and 5 mM threonine, and nearly 1% continued to grow after 16 weeks of selection. A phosphinothricin (PPT) selection system for Agrobacterium-mediated chickpea transformation was also developed. Three varieties of chickpea, P-362, P-1042 and P-1043, were successfully used for Agrobacterium transformation. Following Agrobacterium infection, 3-8% of the regenerated shoots remained green and continued to grow on MSB5 medium supplemented with 2.5 mg l(-1 )PPT. Increasing the concentrations of PPT to 15 mg l(-1) reduced transgenic shoot production in P-362, P-1042 and P-1043 to 0.7%, 1.2% and 1.1%, respectively. Selected putatively transformed shoots of all three varieties were rooted and grown to maturity. Southern hybridization analysis revealed single as well as multiple integration of genes in selected transgenic lines. The level of AK activity detected in LT-selected plants was higher than that detected in the non-transformed control.
一种脱敏天冬氨酸激酶(AK)基因已被开发用作非抗生素选择标记,用于转基因鹰嘴豆(Cicer arietinum L.)的生产。用脱敏AK基因轰击胚外植体再生的转基因芽在含有赖氨酸和苏氨酸(LT)两种氨基酸的培养基上进行筛选。在含有2 μM噻二唑素(TDZ)、2 mM赖氨酸和2 mM苏氨酸的MSB5培养基(MS矿质盐和B5维生素)上生长4周后,P - 362和P - 1042品种约15%的推定转基因芽存活下来。这些芽随后在添加了2 μM TDZ、5 mM赖氨酸和5 mM苏氨酸的MSB5培养基上生长,经过16周筛选后,近1%的芽继续生长。还开发了一种用于农杆菌介导的鹰嘴豆转化的草铵膦(PPT)选择系统。三个鹰嘴豆品种P - 362、P - 1042和P - 1043成功用于农杆菌转化。农杆菌感染后,3 - 8%的再生芽保持绿色,并在添加了2.5 mg l(-1) PPT的MSB5培养基上继续生长。将PPT浓度提高到15 mg l(-1),P - 362、P - 1042和P - 1043的转基因芽产量分别降至0.7%、1.2%和1.1%。所有三个品种选定的推定转化芽生根并生长至成熟。Southern杂交分析显示,选定的转基因系中存在基因的单拷贝和多拷贝整合。在LT选择的植株中检测到的AK活性水平高于未转化对照中检测到的水平。