Current strategies for cDNA cloning are based on construction of cDNA libra
ries and colony screening, The process of obtaining a full length cDNA clon
e can be highly time and labor intensive. Using the human actin gene as a m
odel target cDNA, we have developed an RNA-capture method for rapid cloning
of full-length cDNAs. The approach involves the capture of mRNA with expre
ssed sequence tag (EST)derived, biotin labeled antisense 'capture' primers
and streptavidin-coated magnetic beads. Full-length cDNA is then synthesize
d from purified EST-specific mRNA and cloned directly into plasmid vectors.
The results of using beta -actin-based capture primers on cytoplasmic RNA
were the isolation of both beta- and gamma -actin cDNA clones. Of the 16 ac
tin-specific cDNA clones analyzed, 15 (93%) were full-length. This approach
for cloning full-length cDNAs from available ESTs or partial cDNA sequence
s will facilitate a more rapid and efficient characterization of gene struc
ture and function. (C) 2001 Elsevier Science B.V. All rights reserved.