Genotypes of the two parental strains and representative recombinant progeny at the 18 markers screened in this study.

This table only includes the two parent strains and three highlighted unique meiotic progeny (see below). For the list including all recombinant progeny please see Table S2.
a: Mating types were determined based on mating assay by backcrossing each progeny to the two parental strains. “a” indicates MATa progeny; “α” indicates MATα progeny; “n.a.” indicates the progeny did not mate with either parent (i.e. the progeny is sterile).
b: “+” indicates wild type; “−” indicates auxtrophic;
c: polymorphic sites located within the RPO41 gene;
d: polymorphic sites located within the inter-genic region between the RPO41 and BSP2 genes;
e: polymorphic sites located within the BSP2 gene;
f: PCR-RFLP markers, see Table S1;
g: PCR markers, see Table S1;
h: “F1” indicates the strain was isolated from the F1 generation of the laboratory crosses between JEC169 and S13; “N044” indicates the strain is the progeny No. 44 in the series.
I: The nucleotides that underwent gene conversion in the two progeny, F1N044 and F1N251.
J: The only ade2 URA5 progeny, F1N072.