Two approaches were used to correlate the Aedes aegypti genetic linkage map
to the physical map. STS markers were developed for previously mapped RFLP
-based genetic markers so that large genomic clones from cosmid libraries c
ould be found and placed to the metaphase chromosome physical maps using st
andard FISH methods. Eight cosmids were identified that contained eight RFL
P marker sequences, and these cosmids were located on the metaphase chromos
omes. Twenty-one cDNAs were mapped directly to metaphase chromosomes using
a FISH amplification procedure. The chromosome numbering schemes of the gen
etic linkage and physical maps corresponded directly and the orientations o
f the genetic linkage maps for chromosomes 2 and 3 were inverted relative t
o the physical maps. While the chromosome 2 linkage map represented essenti
ally 100% of chromosome 2, similar to 65% of the chromosome 1 linkage map m
apped to only 36% of the short p-arm and 83% of the chromosome 3 physical m
ap contained the complete genetic linkage map. Since the genetic linkage ma
p is a RFLP cDNA-based map, these data also provide a minimal estimate for
the size of the euchromatic regions. The implications of these findings on
positional cloning in A. aegypti are discussed.