A study was conducted on the feasibility of isolating genes and pseudo
genes that map to chromosome 13 by a hybridization-based approach usin
g a 13-specific library and pools of repeat-free cDNA clones. Five pai
rs of cDNA and chromosome 13 genomic clones were identified and charac
terized. Partial or full-length sequence was derived from all cDNAs, a
nd database searches were performed for putative gene identification,
Partial sequence was also obtained from the chromosome 13 genomic clon
es for comparison with those of the hybridizing cDNAs. As a result of
these analyses we identified three genes, a putative homologue of a po
rcine mRNA encoding an unidentified hepatic protein, a putative homolo
gue of a yeast integral membrane protein, and a gene for a translation
ally controlled tumor protein, and two processed pseudogenes, ribosoma
l proteins L23a and S3a. The latter was formerly identified as the v-f
os transformation effector gene, Fte-1, and recently cited as a possib
le candidate for the BRCA2 gene on chromosome 13. All genes and pseudo
genes were localized to cytogenetic bands by in situ hybridization of
metaphase chromosomes with probes derived from the chromosome 13 genom
ic clones.