The increasing accumulation of genomic sequence information has accentuated
the need for new methods to efficiently assess gene function and to prepar
e reagents to study these functions. Toward solving this general problem in
functional genomics, we report a method by which any PCR-amplified open-re
ading frame (ORF) can be noncovalently linked to a eukaryotic promoter and
terminator, and directly injected into animals to produce local gene expres
sion. We also demonstrate that ORFs can be delivered into mice to produce a
ntibodies specific for the encoded foreign protein by simply attaching mamm
alian promoter and terminator sequences. This technology makes it possible
to screen large numbers of genes rapidly for their functions in vivo or to
produce immune responses without the necessity of cloning, bacterial propag
ation, or protein purification.