Evgen'ev M B, Zelentsova H, Shostak N, Kozitsina M, Barskyi V, Lankenau D H, Corces V G
Department of Biology, The Johns Hopkins University, Baltimore, MD 21218, USA.
Proc Natl Acad Sci U S A. 1997 Jan 7;94(1):196-201. doi: 10.1073/pnas.94.1.196.
A hybrid dysgenesis syndrome occurs in Drosophila virilis when males from an established laboratory strain are crossed to females obtained from the wild, causing the simultaneous mobilization of several different transposable elements. The insertion sequence responsible for the mutant phenotype of a dysgenic yellow allele has been characterized and named Penelope. In situ hybridization and Southern analyses reveal the presence of more than 30 copies of this element in the P-like parental strain, whereas Penelope is absent in all M-like strains tested. Penelope contains one 2.5-kb-long ORF that could encode products with homology to integrase and reverse transcriptase. Northern analysis and whole-mount in situ hybridization show strong induction of a 2.6-kb RNA in the ovaries of dysgenic females that is expressed at very low levels in the parental strains or in the progeny from the reciprocal cross. Injection of Penelope-containing plasmids into preblastoderm embryos of an M-like strain results in mutant progeny caused by insertion of Ulysses and perhaps other transposons, suggesting that Penelope expression might be responsible for the observed dysgenesis syndrome and the simultaneous mobilization of other transposable elements.
当将来自一个已建立的实验室品系的雄性果蝇与从野外获得的雌性果蝇杂交时,在粗壮果蝇中会出现一种杂种发育异常综合征,这会导致几种不同的转座元件同时被激活。导致一种发育异常的黄色等位基因突变表型的插入序列已被鉴定并命名为佩内洛普。原位杂交和Southern分析表明,在P类亲本品系中存在30多个这种元件的拷贝,而在所有测试的M类品系中均不存在佩内洛普。佩内洛普包含一个2.5 kb长的开放阅读框,该阅读框可以编码与整合酶和逆转录酶具有同源性的产物。Northern分析和整体原位杂交显示,在发育异常的雌性果蝇卵巢中强烈诱导出一种2.6 kb的RNA,而该RNA在亲本品系或反交后代中表达水平极低。将含有佩内洛普的质粒注射到M类品系的胚盘前胚胎中会导致由尤利西斯及可能其他转座子插入引起的突变后代,这表明佩内洛普的表达可能是观察到的发育异常综合征以及其他转座元件同时被激活的原因。