Salaj Terézia, Moravcíková Jana, Grec-Niquet Laurence, Salaj Ján
Institute of Plant Genetics and Biotechnology, Slovak Academy of Sciences, Akademická 2, P.O. Box 39 A, 950 07, Nitra 1, Slovak Republic.
Biotechnol Lett. 2005 Jul;27(13):899-903. doi: 10.1007/s10529-005-7178-4.
The stable transformation of embryogenic tissues of Pinus nigra Arn., cell line E104, has been achieved using a biolistic approach. The introduced DNA consisted of the uidA reporter gene under the control of the double CaMV 35S promoter and the nptII selection gene controlled by the single CaMV 35S promoter. Three days after bombardment, putative transformed tissues were selected for continued proliferation on a medium containing 20 mg geneticin l(-1). Resistant embryogenic tissue recovery required 10-12 weeks. The integration of the nptII and uidA genes was confirmed by both histochemical/fluorimetric GUS assays and PCR amplification of the inserts in the five geneticin resistant sub-lines of line E104. The activity of the uidA reporter gene in transgenic, embryogenic tissue lines was stable and could be detected after one year of culture. Somatic embryo maturation was, however, poor and no plantlet regeneration could be obtained.
利用生物弹道法已实现了黑松(Pinus nigra Arn.)胚性组织细胞系E104的稳定转化。导入的DNA由受双CaMV 35S启动子控制的uidA报告基因和受单CaMV 35S启动子控制的nptII选择基因组成。轰击三天后,在含有20 mg遗传霉素l(-1)的培养基上选择假定的转化组织以继续增殖。抗性胚性组织的恢复需要10 - 12周。通过组织化学/荧光GUS分析和对E104品系的五个遗传霉素抗性亚系中的插入片段进行PCR扩增,证实了nptII和uidA基因的整合。uidA报告基因在转基因胚性组织系中的活性是稳定的,并且在培养一年后仍可检测到。然而,体细胞胚胎成熟较差,无法获得植株再生。