Sourceldescription:A sheep genomic fragment from a Sau3A size selected (approx. 500bp) M13mp19 library was selected by hybridization to poly(dC-dA).poly(dG-dT). The cloned fragment was designated MAF65. Sequencing of MAF65 provided the necessary information for polymerase chain reaction (PCR) primer synthesis. The dinculeotide repeat sequence within the 125-bp fragment of MAF65 was of the form (AC)*,,. The sequence of this locus has been submitted to Genbank (Accession number, M67437).Primer sequences: AAAGGCCAGAGTATGCAATTAGGAG(GT strand), CCACTCCTCCTGA-GAATATAACATG(CA strand). These primers are available from the authors' laboratory.
Mendelian inheritance:Segregation was observed in 10 two-generation families containing a total of 46 individuals. The data were consistent with six codominantly inherited alleles, designated according to the number of base pairs detected in the fragment after PCR amplification. Segregation of two of these alleles is demonstrated in the pedigree shown in Fig. 1. Frequency: Estimated from 50 unrelated sheep (24 male, 26 female), from six different breeds (Romney, Merino, Coopworth, Perendale, Texel, and Finnish Landrace.) PIC = 0.62.