Biémont C, Lemeunier F, Garcia Guerreiro M P, Brookfield J F, Gautier C, Aulard S, Pasyukova E G
Laboratoire de Biométrie, Génétique, Biologie des populations, URA C.N.R.S. 243, Université Lyon, Villeurbanne, France.
Genet Res. 1994 Jun;63(3):197-212. doi: 10.1017/s0016672300032353.
The insertion site polymorphism of the copia, mdg1, mdg3, gypsy, and P transposable elements was analysed by in situ hybridization to the polytene chromosomes in genomes of males from a natural population of Drosophila melanogaster. Parameters of various theoretical models of the population biology of transposable elements were estimated from our data, and different hypotheses explaining TE copy number containment were tested. The copia, mdg1 and gypsy elements show evidence for a deficiency of insertions on the X chromosomes, a result consistent with selection against the mutational effects of insertions. On the contrary, mdg3 and P copy numbers fit a neutral model with a balance between regulated transposition and excisions. There is no strong evidence of a systematic accumulation of elements in the distal and proximal regions of the chromosomes where crossing over and ectopic exchanges are reduced. For all chromosome arms but 3L, however, the TE site density increases from the proximal to the distal parts of the chromosomes (the centromeric regions were excluded in this analysis) with sometimes a sharp decrease in density at the extreme tip, following in part the exchange coefficient. The way the copy number of TEs is contained in genomes depends thus on the element considered, and on various forces acting simultaneously, indicating that models of TE dynamics should include details of each element.
通过对黑腹果蝇自然种群雄性个体基因组中的多线染色体进行原位杂交,分析了copia、mdg1、mdg3、gypsy和P转座元件的插入位点多态性。根据我们的数据估计了转座元件群体生物学各种理论模型的参数,并对解释转座元件拷贝数控制的不同假设进行了检验。copia、mdg1和gypsy元件显示出X染色体上插入缺失的证据,这一结果与针对插入突变效应的选择一致。相反,mdg3和P的拷贝数符合一个中性模型,即转座和切除之间保持平衡。在染色体的远端和近端区域,交叉和异位交换减少,但没有强有力的证据表明元件有系统地积累。然而,除了3L染色体臂外,对于所有染色体臂,转座元件位点密度从染色体近端到远端部分增加(在该分析中排除了着丝粒区域),有时在极端末端密度急剧下降,部分遵循交换系数变化。因此,基因组中转座元件拷贝数的控制方式取决于所考虑的元件以及同时作用的各种力量,这表明转座元件动态模型应包括每个元件的详细信息。