Geyer P K, Green M M, Corces V G
Department of Biology, Johns Hopkins University, Baltimore, MD 21218.
Proc Natl Acad Sci U S A. 1988 Jun;85(11):3938-42. doi: 10.1073/pnas.85.11.3938.
To understand the molecular basis of the phenotype of gypsy-induced mutations, we have analyzed the structure of phenotypic revertants of the y2 allele, which is caused by the insertion of the gypsy element into the 5' region of the yellow (y) locus. Seven spontaneous revertants examined fall into two different classes. Three of these revertants arose by homologous recombination between the two gypsy long terminal repeats (LTRs), leaving behind a solo LTR. Four additional revertants contain an intact 3' LTR and half of the 5' LTR, but the central portion of gypsy has been replaced by a different 6.5-kilobase transposable element that contains a poly(A) tail. These results suggest that the mutagenic effect of the gypsy element is not due to its insertion into sequences necessary for transcription or to the distancing between the yellow promoter and remote regulatory sequences but is a consequence of idiosyncratic properties of the element itself.
为了理解由gypsy元件诱导的突变表型的分子基础,我们分析了y2等位基因的表型回复体的结构,该等位基因是由gypsy元件插入黄色(y)基因座的5'区域引起的。所检测的七个自发回复体分为两个不同的类别。其中三个回复体是由两个gypsy长末端重复序列(LTR)之间的同源重组产生的,留下了一个单独的LTR。另外四个回复体包含一个完整的3'LTR和5'LTR的一半,但gypsy的中央部分已被一个不同的6.5千碱基可转座元件所取代,该元件含有一个聚腺苷酸尾。这些结果表明,gypsy元件的诱变作用不是由于其插入转录所需的序列中,也不是由于黄色启动子与远程调控序列之间的距离,而是该元件本身特殊性质导致的结果。