Daniels S B, Peterson K R, Strausbaugh L D, Kidwell M G, Chovnick A
Department of Molecular and Cell Biology, University of Connecticut, Storrs 06268.
Genetics. 1990 Feb;124(2):339-55. doi: 10.1093/genetics/124.2.339.
Several studies have suggested that P elements have rapidly spread through natural populations of Drosophila melanogaster within the last four decades. This observation, together with the observation that P elements are absent in the other species of the melanogaster subgroup, has lead to the suggestion that P elements may have entered the D. melanogaster genome by horizontal transmission from some more distantly related species. In an effort to identify the potential donor in the horizontal transfer event, we have undertaken an extensive survey of the genus Drosophila using Southern blot analysis. The results showed that P-homologous sequences are essentially confined to the subgenus Sophophora. The strongest P hybridization occurs in species from the closely related willistoni group. A wild-derived strain of D. willistoni was subsequently selected for a more comprehensive molecular examination. As part of the analysis, a complete P element was cloned and sequenced from this line. Its nucleotide sequence was found to be identical to the D. melanogaster canonical P, with the exception of a single base substitution at position 32. When the cloned element was injected into D. melanogaster embryos, it was able to both promote transposition of a coinjected marked transposon and induce singed-weak mutability, thus demonstrating its ability to function as an autonomous element. The results of this study suggest that D. willistoni may have served as the donor species in the horizontal transfer of P elements to D. melanogaster.
多项研究表明,P 元件在过去四十年中已在黑腹果蝇的自然种群中迅速传播。这一观察结果,连同在黑腹果蝇亚组的其他物种中不存在 P 元件这一观察结果,引发了一种推测,即 P 元件可能是通过水平转移从一些亲缘关系更远的物种进入黑腹果蝇基因组的。为了确定水平转移事件中的潜在供体,我们使用 Southern 印迹分析对果蝇属进行了广泛的调查。结果表明,P 同源序列基本上局限于 Sophophora 亚属。最强的 P 杂交信号出现在亲缘关系密切的威氏果蝇组的物种中。随后选择了一株野生来源的威氏果蝇进行更全面的分子检测。作为分析的一部分,从该品系中克隆并测序了一个完整的 P 元件。发现其核苷酸序列与黑腹果蝇的典型 P 元件相同,只是在第 32 位有一个单碱基替换。当将克隆的元件注射到黑腹果蝇胚胎中时,它既能促进共注射的标记转座子的转座,又能诱导 singed-weak 突变性,从而证明了其作为自主元件发挥作用的能力。这项研究的结果表明,威氏果蝇可能是 P 元件水平转移到黑腹果蝇过程中的供体物种。