Simultaneous genotyping, gene-expression measurement, and detection of allele-specific expression with oligonucleotide arrays

Table 2.

Results of quantitative PCR experiments analyzing allele-specific expression


ORF name

Predicted ASE direction

Self-linkage p-value

Estimated proportion of BY allele based on linkage data

Estimated proportion of BY allele from Q-PCR experiments

P-value for allele-specific expression from Q-PCR experiments
CIS3* ASE-BY 1e-6 0.55 0.55 0.007
HSPI50* ASE-BY 9e-7 0.55 0.54 0.02
MOG1* ASE-BY 4e-6 0.54 0.53 0.004
TIP1* ASE-BY 4e-10 0.70 0.79 0.004
YHR032W* ASE-BY 0.03 0.48 0.44 0.05
ERD2 ASE-BY 4e-7 0.53 0.50 0.76
ITR1 ASE-BY 5e-5 0.54 0.50 0.91
OPI3 ASE-BY 2e-5 0.56 0.50 1.0
SOD1 ASE-BY 3e-6 0.54 0.49 0.32
SEC53 ASE-BY 0.27 0.50 0.51 0.15
CHO2
ASE-BY
0.04
0.52
0.48
0.01
  • The allele predicted to show preferential expression based on the microarray analysis is shown in column 2. We calculated self-linkage p-values as described previously (Brem et al. 2002). The predicted amount of BY allele expressed based in the linkage data was determined by comparing the mean expression level in segregants bearing the BY genotype at the ORF in question to the segregants bearing the RM genotype at this locus. Single astericks indicate ORFs that showed significant allele-specific expression according to quantitative PCR in the direction predicted, thus confirming the array-based detection.

This Article

  1. Genome Res. 15: 284-291

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