Abstract
An improved protocol has been developed for physical enrichment of cDNA sequences by hybridization to genomic DNA. When applied to microdissection recombinants derived from a translocation breakpoint region associated with inherited mental illness, a single cycle of the procedure permitted enriched cDNAs to be visualized directly by agarose gel electrophoresis. Hybridization screening of a library of clones derived from the enriched cDNAs, employing the genomic resource as a probe, led to the identification of six novel gene fragments. This general approach to the isolation of regionally encoded genes could be applied to any subchromosomal interval as a first step towards global transcription map construction.
Original language | English |
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Pages (from-to) | 257-262 |
Number of pages | 6 |
Journal | Mammalian Genome |
Volume | 6 |
Issue number | 4 |
Publication status | Published - 1995 |
Keywords
- Animals Base Sequence Blotting, Southern Brain/*metabolism Callithrix Cats Cattle *Chromosomes, Human, Pair 1 Cricetinae DNA, Complementary/genetics Dogs Electrophoresis, Agar Gel Gene Library Humans Mice Molecular Sequence Data *Nucleic Acid Hybridization Polymerase Chain Reaction Psychotic Disorders/*genetics Rabbits Rats Sheep Species Specificity Swine *Translocation, Genetic