A novel cloning procedure which makes use of covalent attachment of probe D
NA to specific target DNA is reported. We show that specific gene fragments
found in complex genomes such as the human genome can be cloned directly f
rom a pool of genomic DNA with very high efficiency. This direct cloning me
thod totally eliminates certain steps in current cloning procedures such as
construction of DNA libraries and colony (plaque) hybridization, The resul
ting process has made cloning methods simpler and more time efficient, whil
e achieving high cloning efficiency due to the stable nature of the probe-t
arget DNA complex through covalent bonding. Most importantly, since clones
are directly obtained from a pool of genomic DNA, the isolated clones are c
onsidered to be faithful copies of the original genes. This has apparently
solved the problem of isolating clones with misincorporated bases or chimer
ic DNA, both of which are often encountered in cloning processes using PCR
or other methods involving in vitro DNA synthesis.