Porcine flow-sorted Chromosome (Chr) 13 was PCR amplified with primers
based on porcine short interspersed element (SINE) sequences. The pro
duct was cloned, gridded in microtiter plates, and screened with a [GT
](10) oligonucleotide which gave 45 positive clones. Sequencing of the
se clones showed that 36 were unique, and 26 [GT](n) microsatellites w
ere characterized. Six other simple repeat sequences, the majority of
which were associated with the 3' end of the SINE sequence, were also
detected. Twenty-one primers sets were selected, and 13 of these detec
ted useful polymorphisms in the grandparents (n = 26) of the European
porcine mapping collaboration (PiGMaP) reference families. These 13 ma
rkers were mapped in the ''PiGMaP'' reference families, and a two-poin
t linkage analysis was performed. The Lod scores indicated that three
of the markers were not linked and the remaining 11 formed two linkage
groups of two and nine markers respectively. The larger linkage group
was also linked to the transferrin locus, permitting assignment of ni
ne markers to porcine Chr 13.