Table II

Role of Bud Site Selection Genes in Mating

Relevant genotypePrezygote accumulation*Mating frequencyBud site selection§ (axial)
MATα strains    %  %  % 
 FC139  Parental   5  21.0 ± 5.0  92 
 LE49a  axl1Δ  55   6.0 ± 2.0  37 
 LEb1  rsr1Δ  60   4.0 ± 2.0  14 
 LEb3  bud3Δ  44   8.0 ± 0.6  29 
 LE49b1  axl1Δ rsr1Δ  64   5.0 ± 0.6  13 
 LE49b3  axl1Δ bud3Δ  64   5.0 ± 0.1  16 
 LEf14  fus1Δ  41  14.0 ± 0.9  — 
MATa strains         
 LE74x  axl1Δ  51   0.3 ± 0.1  40 
 LEab1  rsr1Δ  83   3.2 ± 0.4   17 
 LEab3  bud3Δ  64   2.6 ± 0.9  — 
Relevant genotypePrezygote accumulation*Mating frequencyBud site selection§ (axial)
MATα strains    %  %  % 
 FC139  Parental   5  21.0 ± 5.0  92 
 LE49a  axl1Δ  55   6.0 ± 2.0  37 
 LEb1  rsr1Δ  60   4.0 ± 2.0  14 
 LEb3  bud3Δ  44   8.0 ± 0.6  29 
 LE49b1  axl1Δ rsr1Δ  64   5.0 ± 0.6  13 
 LE49b3  axl1Δ bud3Δ  64   5.0 ± 0.1  16 
 LEf14  fus1Δ  41  14.0 ± 0.9  — 
MATa strains         
 LE74x  axl1Δ  51   0.3 ± 0.1  40 
 LEab1  rsr1Δ  83   3.2 ± 0.4   17 
 LEab3  bud3Δ  64   2.6 ± 0.9  — 
*

 Prezygote accumulation was determined by microscopic observation as described in Materials and Methods. More than 500 mating pairs were scored for each strain pair. MATa partner is LM23-3az.  

 Mating frequency was measured as the percent of prototrophic diploids formed/total viable cells after limited mating to the MATa partner, LM23-3az, and is the average ± standard deviation of duplicate filter mating determinations.  

§

 The frequency of axial budding (not bipolar or random) was determined. Budding patterns were assayed for >100 microcolonies.  

 Prezygote accumulation and mating frequenices determined as above. The MATα partner for both assays was FC139.  

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