A plasmid library of oat chromosome No21, the smallest chromosome of t
he complement, was constructed by microdissection and microcloning. Th
e chromosome was deproteinized with proteinase K and digested with Sau
3A and linker adaptors were ligated to the DNA fragments. From the sin
gle chromosome (less than 0.4 pg), 10 mu g of DNA was obtained after 2
rounds of PCR amplification. Cloning experiments with the amplified D
NA produced as many as 500 000 recombinant clones from the single chro
mosome. The 500 clones evaluated ranged in size from 150 to 1700 base
pairs (bp) with an average size of 650 bp. These were approximately 41
% high-copy and 59% low/unique copy clones. Tandem repeats were absent
in the library and may have been selected against by a combination of
the Sau3A digestion, which is sensitive to C-methylation, and the PCR
amplification. Many low-copy dispersed repetitive sequences were pres
ent in the library. These were present primarily on A- and D-genome ch
romosomes. Southern blot analysis revealed that the unique-copy clones
were suitable for restriction fragment length polymorphism analysis a
nd that they mapped to the pertinent oat nullisomic lines.