Generating sequence-tagged sites (STSs) is a prerequisite to convert a
genetic map to a physical map. With the help of sequence information
from these STSs one can also isolate specific genes. For these purpose
s, we have designed PCR primer sets, of 20 bases each, by reference to
sequences of restriction fragment length polymorphism (RFLP) landmark
ers consisting of rice genomic clones. These markers were evenly distr
ibuted over the 12 chromosomes and were shown to be single copy by Sou
thern-blot analysis. With improved PCR protocols, 63 standard STS land
markers in the rice genome were generated. Similarity searches of all
partial sequences of RFLP landmarkers by the FASTA algorithm showed th
at 2 of the 63 RFLP landmarkers, G357 and G385, contained part of the
ORFs of aspartate aminotransferase and protein kinase, respectively.