Table 2. PCR primers used in this study.
| Primer | Sequence (5’3’) |
|---|---|
| GPH1BamHIf | CGCGGATCCTGAACAATGCCGCCAGCTAGTAC-3´ |
| GPH1ClaIr | CCCATCGATAGTCACTGGTTCAACGTTCCAAATG-3´ |
| RSB1BamHIf | CGCGGATCCGGTGGTATGGTACCGAACCTTC-3´ |
| RSB1SalIr | CCCGTCGACAAGTTTAGCCTTCTTTTTAGAGGAAAC-3´ |
| GPM2BamHIf | CGCGGATCCATGACTGCAAGCACACCATCCAA-3´ |
| GPM2HindIIIr | CCCAAGCTTAGGATTTTTTATGAAACCCTCATTACGG-3´ |
| Act1-RTfwd | CCAGCCTTCTACGTTTCCATCCAAG |
| Act1-RTrev | GACGTGAGTAACACCATCACCGGA |
| Psd2_RTfw | GCGCCACAAGATTATCACCGGTTTCACTC |
| Psd2_RTrev | CTAACTCACTACGAACGGCCATTGGATTTACAG |
| Ale1_RTfw | CTTGCGAGAAGATGGTGTCACTCCTTTG |
| Ale1_RTrev | GGTTGCACCATGTAACCAAATGCTAGTTTAATTG |
| Eki_RTfw | CAATCTAATCATCGAATGGAGGCCTTGTACAC |
| Eki_RTrev | CATCACCTAGTCCAGCCTTTTCGCTC |
| Ect1_RTfw | GCCGTTATTATCGATGCTGACGCCAC |
| Ect1_RTrev | GTCAAGTATTCACTGAATTTTCCGGCAGCAG |
| Ept_RTfw | CTCTTTCATCCTTTCCGTTGGTTTCACGGGAG |
| Ept_RTrev | CATGGGTGCATTGAACATGGGAAAGCTC |
| Dpl1_RTfw | GTCGTGCCAAGAAATAGTCGGTGCAGCAATG |
| Dpl1_RTrev | GACTGAATATCTAGGGTTGCCCATTATATTCAGGTCTG |
| Gph1_RTfw | CCACGCAAGGTTTCAATCTTTGGTGGTAAGAG |
| Gph1_RTrev | CGTCGTTATTAACAATGTCAGCAACACAGTTGATC |
| Gpm2_RTfw | GTGGGCCATGGAAGTTCAGTGAGATC |
| Gpm2_RTrev | CAACGACTAAGGGGATACCATTTGGAATATCAAC |
| Rsb1_RTfw | GATGGCCATCGCTACGGTCACTTTG |
| Rsb1_RTrev | GTAAAGTTTCAGGATCAACATGGCCCGGTG |
Upper part: PCR primers used for the amplification of genes. Recognition sites for restriction enzymes are underlined. Lower part: Primers used for qRT-PCR.