Jouan-Dufournel I, Cosset F L, Contamine D, Verdier G, Biémont C
Laboratoire de Biométrie, Génétique et Biologie des Populations, UMR 5558, Université Claude Bernard, Lyon 1, 69622 Villeurbanne Cedex, France.
J Mol Evol. 1996 Jul;43(1):19-27. doi: 10.1007/BF02352295.
To analyze the behavior of endogenous transposable elements under genomic stress, a Drosophila melanogaster inbred line was submitted to three kinds of viral perturbations. First, a retroviral plasmid containing the avian Rous Associated Virus type 2 (RAV-2) previously deleted for the viral envelope coding gene (env) was introduced by P element transformation into the Drosophila genome. An insertion of this avian retroviral sequence was detected by in situ hybridization in site 53C on polytene chromosome arm 2R. Second, Drosophila embryos were injected with RAV-2 particles produced by cell culture after transfection with the retroviral plasmid. Third, the Drosophila melanogaster inbred line was stably infected by the sigma native virus. It appears that neither the offspring of the flies in which the viral DNA was found integrated nor those from the infected sigma flies showed copia or mdg1 element mobilization. Injection of the avian RAV-2 particles led, however, to the observation of somatic transpositions of mdg1 element on the 2L chromosome, the copia element insertion pattern remaining stable. Thus, endogenous transposable elements show more instability in sublines injected with exogenous viral particles than in a transgenic subline containing a foreign viral insert, all transposable elements not being equally sensitive to such genomic stress.
为了分析基因组应激下内源性转座元件的行为,将一种黑腹果蝇近交系进行三种病毒干扰处理。首先,通过P因子转化将一个先前已缺失病毒包膜编码基因(env)的禽2型劳斯相关病毒(RAV - 2)逆转录病毒质粒导入果蝇基因组。通过原位杂交在多线染色体臂2R的53C位点检测到该禽逆转录病毒序列的插入。其次,用逆转录病毒质粒转染细胞培养产生的RAV - 2颗粒注射果蝇胚胎。第三,黑腹果蝇近交系被西格玛天然病毒稳定感染。似乎在发现病毒DNA整合的果蝇后代以及感染西格玛病毒的果蝇后代中,均未观察到copia或mdg1元件的转座。然而,注射禽RAV - 2颗粒导致在2L染色体上观察到mdg1元件的体细胞转座,copia元件的插入模式保持稳定。因此,与含有外源病毒插入片段的转基因亚系相比,注射外源病毒颗粒的亚系中的内源性转座元件表现出更大的不稳定性,并非所有转座元件对这种基因组应激都同样敏感。