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[ T + N] heterokaryons produced homokaryotic conidial derivatives of both mating types, but [ Dp + Df] heterokaryons produced viable conidial homokaryons of only the mating type of the Dp nucleus.
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This information could explain the apparent asexuality of the populations we sampled (for example, only one mating type may be present), or suggest that asexual reproduction is dominant at broader geographic scales if both mating types are co-occurring but no evidence of recombination is observed.
We found both mating types were present in all populations and mating-type ratios did not deviate from 1 1.
Among the 564 randomly selected deletion strains, 2.7% (15/564) were significantly long-lived in both mating types, while 4.3% (24/564) were long-lived if data were pooled for both mating types (Table 1).
The latter occurs when both mating types, MATa and MATα, secrete a pheromone (a-factor or α-factor, respectively) to which the opposite mating type expresses the cognate G protein-coupled receptor (GPCR).
III in both mating types.
Gametes of both mating types produce attractive pheromones used to signal to the other mating type.
Both mating types were retained (FY5216: h + or FY5217: h −).
Both mating types can act as males or females.
Of the 24 AD hybrid isolates with designated serotype/mating type, seven had only one mating type (MATα; αADα) and 17 had both mating types (12 aADα and 5 αAD a) present in their diploid genomes.
Only a single population was found that did not include both mating types.
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