Yang C H, Ellis J G, Michelmore R W
Department of Vegetable Crops, University of California, Davis 95616.
Plant Mol Biol. 1993 Aug;22(5):793-805. doi: 10.1007/BF00027366.
The maize transposable element Activator (Ac) is being used to develop a transposon mutagenesis system in lettuce, Lactuca sativa. Two constructs containing the complete Ac from the waxy-m7 locus of maize were introduced into lettuce and monitored for activity using Southern analysis and PCR amplification of the excision site. No transposition of Ac was detected in over 32 transgenic R1 plants, although these constructs were known to provide frequent transposition in other species. Also, no transposition was observed in later generations. In subsequent experiments, transposition was detected in lettuce calli using constructs that allowed selection for excision events. In these constructs, the neomycin phosphotransferase II gene was interrupted by either Ac or Ds. Excision was detected as the ability of callus to grow on kanamycin. Synthesis of the transposase from the cDNA of Ac expressed from the T-DNA 2' promoter resulted in more frequent excision of Ds than was observed with the wild-type Ac. No excision was observed with Ds in the absence of the transposase. The excision events were confirmed by amplification of the excision site by PCR followed by DNA sequencing. Excision and reintegration were also confirmed by Southern analysis. Ac/Ds is therefore capable of transposition in at least calli of lettuce.
玉米转座元件激活子(Ac)正被用于在生菜(Lactuca sativa)中开发转座子诱变系统。将两个含有来自玉米蜡质 - m7位点完整Ac的构建体导入生菜,并使用Southern分析和切除位点的PCR扩增监测其活性。在超过32株转基因R1植株中未检测到Ac的转座,尽管已知这些构建体在其他物种中能频繁转座。此外,在后代中也未观察到转座现象。在随后的实验中,使用允许选择切除事件的构建体在生菜愈伤组织中检测到了转座。在这些构建体中,新霉素磷酸转移酶II基因被Ac或Ds中断。切除被检测为愈伤组织在卡那霉素上生长的能力。由T - DNA 2'启动子表达的Ac cDNA合成的转座酶导致Ds的切除比野生型Ac更频繁。在没有转座酶的情况下,未观察到Ds的切除。通过PCR扩增切除位点并进行DNA测序证实了切除事件。Southern分析也证实了切除和重新整合。因此,Ac/Ds至少在生菜愈伤组织中能够转座。