Molecular cloning of sequences from a drosophila RNA polymerase II locus by P element transposon tagging

We have identified a lethal mutation in the D. melanogaster RNA polymerase II locus, Rpll^C4, caused by insertion of a transposable element associated with the phenomenon of hybrid dysgenesis (P element). Using previously cloned P element sequences as a hybridization probe we have isolated a hybrid lambda phage clone carrying a 10 kb genomic DNA fragment containing a 1.3 kb P element insert and flanking sequences from the Rpll locus. The non-P sequences in this clone (λDmRpll-1) hybridize to polytene chromosome band region 10C, the cytogenetic location of Rpll^C4, and revertants which lose the lethal RNA polymerase II mutation also lose P element sequences from the locus. We have generated several additional P element insertions into the locus and shown that they can occur at two or more different sites. These experiments illustrate that mutagenesis by P element insertion and use of cloned P DNA to retrieve the DNA sequences into which insertion has occurred may be a general method for cloning genetically defined loci in Drosophila.