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. 2007 Nov;177(3):1609–1620. doi: 10.1534/genetics.107.078386

TABLE 1.

spd-3 SNP map

Cosmid Primers Enzyme
C31H1 AAAACTGGTCGAGGCACAC HpyCH4IV
AGCCACGTAGCCACTGTAAC
C49A9 TTTTGTTGTCGCATCACTTCTG SspI
AACTTCTAAATGCTGCCCTTCC
T13A10 GCTTGAGTGCCAGTTGTTATGTG
CTGCGGAAAAGGGTATGAGAA
Y73B6Bl CCTGCAGGTGCGGATTGAG
CTAACCGATGCGCTGTGAACG
F38A5 GCACCATCTTCTGCTCCAAC XbaI
TTAACCTTTGGAGTGACTGCG
Y73B6A TTATAGCTTGAACAACGGGACATC
CTCATTCGTTCGTGCTATTTCTCT
H34C03 TCCGCCAATTTCCAC
CATCATGCGCCCACTTCT
R13H7 ACAAGATCGTTTTCAGGGTCAAT
AGGGGGAGAATAAAACATCGTAA
B0478 AAGAAGTGCCACCCAAAAAGAG
AAACCTAGCCGCCAAATGAC
C25A8 CCCTTATGCCATTACTTATTCGTG
GTCGCCGGCGTTTTTACTTT
Y43B11AR TTCGCAGTAGTAAAAGGTAAACAA BsrSI
CGGCGACGGCGAGAAGT
D2024 TAACCGCCACGAAAAAGATAGGAT
GGGACTTAGAATTACTGCGTTTGA
C48A7 TGGTGCACGAAGAAGGAAGAG DraI
GCCCCCGGAAATCAGAAATG
R05G6 GGTGTTCAAACATGCGACG PstI
TTTGGACGGATAGCTACATACG

A single-nucleotide polymorphism (SNP) map was designed for spd-3 mapping. Primers were designed using DNAStar Lasergene PrimerSelect and used to amplify ∼1 kb of DNA containing a SNP between the Bristol and the Hawaiian strain. Several of these SNPs were contained in restriction enzyme cut sites in one strain but not the other, in which case the appropriate restriction enzymes were used to determine the genotype of the recombinant strain. In other cases, strains were genotyped by sequencing (no enzyme listed).