Cho M-J, Ha C D, Lemaux P G
Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720, USA e-mail:
Plant Cell Rep. 2000 Nov;19(11):1084-1089. doi: 10.1007/s002990000238.
Highly regenerative tissues of tall fescue and red fescue produced from mature seed-derived embryogenic callus were induced and proliferated on medium containing 2,4-dichlorophenoxyacetic acid (4.5 or 9.0 μM), 6-benzylaminopurine (0, 0.044, 0.44 or 2.2 μM) and cupric sulfate (0.1 or 5.0 μM) under dim-light conditions (10 to 30 μE m s, 16 h light). Tall fescue tissues were transformed with three plasmids containing the genes for hygromycin phosphotransferase (hpt), phosphinothricin acetyltransferase (bar) and β-glucuronidase (uidA;gus), and red fescue with three plasmids containing hpt, uidA and a synthetic green fluorescent protein gene [sgfp(S65T)]. DNA from T plants of eight independently transformed lines from tall fescue and 11 from red fescue were analyzed by PCR and DNA blot hybridization. The co-expression frequency of all three transgenes [hpt/bar/uidA or hpt/uidA/sgfp(S65T)] in transgenic tall fescue and red fescue plants was 25-27%; for two transgenes [hpt/bar or hpt/uidA for tall fescue and hpt/uidA or hpt/sgfp(S65T) for red fescue], the co-expression frequency was 50-75%.
由成熟种子来源的胚性愈伤组织诱导产生的高羊茅和紫羊茅的高再生组织,在含有2,4-二氯苯氧乙酸(4.5或9.0μM)、6-苄基腺嘌呤(0、0.044、0.44或2.2μM)和硫酸铜(0.1或5.0μM)的培养基上,于弱光条件下(10至30μE m s,16小时光照)进行增殖。用含有潮霉素磷酸转移酶(hpt)、草丁膦乙酰转移酶(bar)和β-葡萄糖醛酸酶(uidA;gus)基因的三种质粒转化高羊茅组织,用含有hpt、uidA和合成绿色荧光蛋白基因[sgfp(S65T)]的三种质粒转化紫羊茅组织。对来自高羊茅的8个独立转化株系和紫羊茅的11个独立转化株系的T植株的DNA进行PCR和DNA印迹杂交分析。转基因高羊茅和紫羊茅植株中所有三个转基因[hpt/bar/uidA或hpt/uidA/sgfp(S65T)]的共表达频率为25-27%;对于两个转基因[高羊茅的hpt/bar或hpt/uidA以及紫羊茅的hpt/uidA或hpt/sgfp(S65T)],共表达频率为50-75%。