Lyubomirskaya N V, Avedisov S N, Surkov S A, Ilyin Y V
V.A. Engelghardt Institute of Molecular Biology, Academy of Sciences of Russia, Moscow.
Nucleic Acids Res. 1993 Jul 11;21(14):3265-8. doi: 10.1093/nar/21.14.3265.
Plasmid DNA constructs containing 5' end truncated retrotransposon gypsy were introduced into Drosophila cultured cells. Appearance of new complete DNA copies with reconstructed via reverse transcription 5'LTR were detected by PCR after transient expression and by Southern blot analysis of genome DNA of stably transformed cells. Two gypsy subfamilies supposed to be different in transpositional activity were analyzed in terms of their ability to produce new DNA copies via reverse transcription in D. hydei cultured cells. It was demonstrated that both gypsy variants undergo retrotransposition but with different efficiency.
将含有5'端截短的逆转座子吉普赛(gypsy)的质粒DNA构建体导入果蝇培养细胞。在瞬时表达后通过PCR以及对稳定转化细胞的基因组DNA进行Southern印迹分析,检测到通过逆转录重建了5'长末端重复序列(LTR)的新的完整DNA拷贝。分析了两个推测在转座活性上不同的吉普赛亚家族在海德氏果蝇(D. hydei)培养细胞中通过逆转录产生新DNA拷贝的能力。结果表明,两种吉普赛变体都经历逆转座作用,但效率不同。