Blackman R K, Koehler M M, Grimaila R, Gelbart W M
Department of Cellular and Developmental Biology, Harvard University, Cambridge, MA 02138-2097.
EMBO J. 1989 Jan;8(1):211-7. doi: 10.1002/j.1460-2075.1989.tb03366.x.
The transposable element hobo can be mobilized to induce a variety of genetic abnormalities within the germ-line of Drosophila melanogaster. Strains containing hobos have 3.0 kb elements and numerous smaller derivatives of the element. By analogy with other transposable element systems, it is likely that only the 3.0 kb elements are capable of inducing hobo mobilization. Here, we report that a cloned 3.0 kb hobo, called HFL1, is able to mediate germ-line transformation and therefore is an autonomous (fully-functional) transposable element. Germ-line transformation was observed when HFL1 and a marked hobo element were co-injected into recipient embryos devoid of endogenous hobos. Integration did not occur in the absence of the 3.0 kb element. A single copy of the marked hobo transposon inserted at each site, and the target sites were widely distributed throughout the genome. Integration occurred at (or very near) the termini of hobo, without internal rearrangement of the hobo or marker gene sequences. The hobo transformation system will allow us to determine the structural and regulatory features of hobo responsible for its mobilization and will provide novel approaches for the molecular and genetic manipulation of the Drosophila genome.
转座因子hobo能够被激活,从而在黑腹果蝇的种系中诱导出各种遗传异常。含有hobo的品系具有3.0 kb的元件以及该元件的许多较小的衍生物。与其他转座因子系统类似,可能只有3.0 kb的元件能够诱导hobo转座。在此,我们报道了一个克隆的3.0 kb的hobo,称为HFL1,它能够介导种系转化,因此是一个自主的(功能完全的)转座因子。当将HFL1和一个带有标记的hobo元件共同注射到没有内源性hobo的受体胚胎中时,观察到了种系转化。在没有3.0 kb元件的情况下不会发生整合。在每个位点插入了单拷贝的带有标记的hobo转座子,并且靶位点广泛分布于整个基因组中。整合发生在hobo的末端(或非常接近末端的位置),hobo或标记基因序列没有内部重排。hobo转化系统将使我们能够确定负责其转座的hobo的结构和调控特征,并将为果蝇基因组的分子和遗传操作提供新的方法。