A set of 100 restriction fragment length polymorphism (RFLP) markers
on the Cornell-IRRI genetic map of rice were converted into
sequence-tagged sites by terminal DNA sequencing. Fifty of the
markers were RG random genomic clones and the other fifty were RZ cDNA
clones. Oligonucleotide pairs were synthesized for the amplication of
the marker loci by the polymerase chain reaction (PCR). All primer
pairs amplified marker loci in Oryza sativa and O. longistaminata.
The frequencies of amplicon length > polymorphisms (ALPs) and
PCR-based RFLPs were determined within O. sativa, within the 8 AA
genome species, within the genus Oryza, and between Oryza and related
genera such as Porteresia. The data provide an indication of the
range of evolutionary diversity over which sequence-tagged sites
consitiute useful markers.
Supported by RF and BMZ/GTZ.