Modern molecular genetic and genomic approaches are revolutionizing th
e study of behavior in the mouse. ''Reverse genetics'' (from gene to p
henotype) with targeted gene transfer provides a powerful tool to diss
ect behavior and has been used successfully to study the effects of nu
ll mutations in genes implicated in the regulation of long-term potent
iation and spatial learning in mice. In addition, ''forward genetics''
(from phenotype to gene) with high-efficiency mutagenesis in the mous
e can uncover unknown genes and has been used to isolate a behavioral
mutant of the circadian system. With the recent availability of high-d
ensity genetic maps and physical mapping resources, positional cloning
of virtually any mutation is now feasible in the mouse. Together, the
se approaches permit a molecular analysis of both known and previously
unknown genes regulating behavior.