Table 1. Oligonucleotide primers used in the PCR amplification of various transcription factors.

Use	Gene	Primer Sequence
cDNA cloning	dappuPNR	forward: 5′-AGTATCCCAACGGAGTGACG-3′
		reverse: 5′-TACTGAGGATCCCGGGTCA-3′
cDNA cloning	dappuDSF	forward: 5′-CATCGTCTCCCCTCCTTGTA-3′
		reverse: 5′-GGGGGAAAGGAAATCTCATC-3′
cDNA cloning	dappu & dapmag Met	forward: 5′-CCTTACGGAAAGCATCTTTAGTG-3′
		reverse: 5′-CGTATGAATTAAAACAGCTTATTAGAAGTC-3′
Reporter Assay	GAL4	forward: 5′- TATT ACTAGTGGCATGAAGCTACTGTCTTCTATCGAACAAG-3′
		reverse: 5′- AATT TTCGAATCTAGATGATATCAACGCGTCAAGTCGAC-3′
Reporter Assay	dappuPNR	forward: 5′-TACTAT GAATTCCGACCGGAAATTCTGGCCGAA-3′
		reverse: 5′-TACTAT TTCGAATTAATTTTTGTACATATCGCAGAG-3′
Reporter Assay	dappuDSF	forward: 5′-CAAC GAATTCAACAGCGTCCATCACCATTTC-3′
		reverse: 5′-CTCT TTCGAACATCGATGAAACCAAACCAA-3′
Reporter Assay	dappuMet	forward: 5′-TACTAT GAATTCATACATCAGAATGTGGATTTACGGGT-3′
		reverse: 5′-TACTAT ACGCGTTCACGGACTACTAGTTCCAG-3′

Bold denotes added restriction sites and italics denote spacer nucleotides added to facilitate proper cutting of the sequence. Some primers used in the reporter assay constructs were situated upstream or downstream of the sequence targeted for amplification.