Baldrich E, Dimitri P, Desset S, Leblanc P, Codipietro D, Vaury C
Dipartimento di Genetica e Biologia Molecolare, Universita di Roma La Sapienza, Italy.
Genetica. 1997;100(1-3):131-40.
The mobile element ZAM, recently identified in Drosophila melanogaster, is similar in structure and coding potential to vertebrate retroviruses. In this paper, we analyze the insertional and structural polymorphism of this element and show that members of this family appear to have a long evolutionary history in the genome of Drosophila. It is present in all the species of the D. melanogaster subgroup and in more distantly related species like D. takahashii, D. ananassae, or D. virilis but in a lower copy number or with a lower homology. Two categories of strains have been previously identified in D. melanogaster: strains with a high copy number of ZAM and strains with a low copy number. Here, we show that ZAM is at least in a low copy number in each tested strain of the species analyzed. The study of ZAM's genomic distribution by FISH mapping analysis to salivary gland polytene chromosomes or on mitotic chromosomes indicates that most of the insertion sites of ZAM elements are associated with the constitutive heterochromatin regardless of the ZAM copy number. In addition, our results suggest that multiple ZAM elements are present at the insertion sites visualized by in situ experiments.
最近在黑腹果蝇中发现的移动元件ZAM,在结构和编码潜能上与脊椎动物逆转录病毒相似。在本文中,我们分析了该元件的插入和结构多态性,并表明这个家族的成员在果蝇基因组中似乎有着漫长的进化历史。它存在于黑腹果蝇亚组的所有物种中,以及在亲缘关系较远的物种如高桥氏果蝇、拟果蝇或果蝇中,但拷贝数较低或同源性较低。先前在黑腹果蝇中已鉴定出两类品系:ZAM拷贝数高的品系和拷贝数低的品系。在这里,我们表明在所分析物种的每个测试品系中ZAM至少处于低拷贝数状态。通过荧光原位杂交(FISH)图谱分析唾液腺多线染色体或有丝分裂染色体来研究ZAM的基因组分布,结果表明,无论ZAM的拷贝数如何,ZAM元件的大多数插入位点都与组成型异染色质相关。此外,我们的结果表明,原位实验观察到的插入位点存在多个ZAM元件。