Weld R, Heinemann J, Eady C
Plant and Microbial Sciences Department, University of Canterbury, Christchurch, New Zealand.
Plant Mol Biol. 2001 Mar;45(4):377-85. doi: 10.1023/a:1010798625203.
The transient nature of T-DNA expression was studied with a gfp reporter gene transferred to Nicotiana plumbaginifolia suspension cells from Agrobacterium tumefaciens. Individual GFP-expressing protoplasts were isolated after 4 days' co-cultivation. The protoplasts were cultured without selection and 4 weeks later the surviving proto-calluses were again screened for GFP expression. Of the proto-calluses initially expressing GFP, 50% had lost detectable GFP activity during the first 4 weeks of culture. Multiple T-DNA copies of the gfp gene were detected in 10 of 17 proto-calluses lacking visible GFP activity. The remaining 7 cell lines contained no gfp sequences. Our results confirm that transiently expressed T-DNAs can be lost during growth of somatic cells and demonstrate that transiently expressing cells frequently integrate multiple T-DNAs that become silenced. In cells competent for DNA uptake, cell death and gene silencing were more important barriers to the recovery of stably expressing transformants than lack of T-DNA integration.
利用从根癌农杆菌转移至烟草悬浮细胞中的绿色荧光蛋白(gfp)报告基因,研究了T-DNA表达的瞬时特性。共培养4天后,分离出表达绿色荧光蛋白的单个原生质体。原生质体在无选择条件下培养,4周后,再次筛选存活的原愈伤组织以检测绿色荧光蛋白表达情况。在最初表达绿色荧光蛋白的原愈伤组织中,50%在培养的前4周内失去了可检测到的绿色荧光蛋白活性。在17个缺乏可见绿色荧光蛋白活性的原愈伤组织中,有10个检测到gfp基因的多个T-DNA拷贝。其余7个细胞系不含gfp序列。我们的结果证实,瞬时表达的T-DNAs在体细胞生长过程中可能会丢失,并表明瞬时表达的细胞经常整合多个沉默的T-DNAs。在能够摄取DNA的细胞中,细胞死亡和基因沉默比缺乏T-DNA整合更重要,是稳定表达转化体回收的障碍。