A PCR-based sequence-tagged site (STS) content mapping strategy has be
en used to generate a physical map with 90% coverage of the 120-Mb euc
hromatic portion of the Drosophila genome. To facilitate map completio
n, the bulk of the STS markers was chosen in a nonrandom fashion. To e
nsure that all contigs were localized in relation to each other and th
e genome, these contig-building procedures were performed in conjuncti
on with a large-scale in situ hybridization analysis of randomly selec
ted clones from a Drosophila genomic library that had been generated i
n a P1 cloning vector. To date, the map consists of 649 contigs with a
n STS localized on average every 50 kb. This is the first whole genome
that has been mapped based on a library constructed with large insert
s in a vector that is maintained in Escherichia coli as a single-copy
plasmid.