Table 1.

Primers employed for Q-PCR experiments.

Arabidopsis genes	Sequence	Amplified fragment size (bp)
CO	5′ -CCAATGGACAGAGAAGCCAGG-3′ 5′ -GCATCGTGTTGAACCCTTGC- 3′	175
AtSSS	5′ -CTGGGGATCATCAGCTACACAATACG-3′ 5′ -CACGTGCGATTAGGAACAGCTC-3′	81
AtFAD	5′- CGTCGTTAAGTTCCTTCAAGCC -3′ 5′- CATAGCTTCAATCGAACCGACAG -3′	157
AtGS	5′- CCAGCTTCGAACATGGATCC -3′ 5′-CCTAAGACATTGCTTGATAGAGAACAC-3′	167
AtZEP	5′- CTCCGAAATCGACGAGGAAG -3′ 5′- TGCAAGGAATAGCTGAAAGCAG -3′	166
AtUBQ10	5′- GAAGTTCAATGTTTCGTTTCATGT -3′ 5′- GGATTATACAAGGCCCCAAAA -3′	119
AtERF	5′- CCAATGTTCAGCAGAATGCC -3′ 5′- GGACGATGAGAAAGAATTAGGAG -3′	85
AtWRKY33	5′-TACCGGGCCTTTTGGTTA-3′ 5′- CCACCACCAACAAAGTTTTG-3′	81
Chlamydomonas genes	Sequence	bp
CrCO	5′- CTTCCCGCAAGGCGTATGC -3′ 5′- GCCTCAATCTCCTCCTTCTTGGC -3′	73
CrSSS	5′- ACGTGTACCGCTCCATCAGC -3′ 5′- GCAGCACTCTTGCACTATGCAG -3′	107
CrFAD	5′- GACGAGAAGGTCAACTACAAGCC -3′ 5′- GCTTGCTCAGCTCCGATTAGC -3′	150
CrGS	5′- GCTACGGCTACCTGGAGGA -3′ 5′- CATCGCTGCCCTTATTAGCTGG -3′	127
CrZEP	5′- AAGAGGCAGGTTGGCTTAGTGC -3′ 5′- GGTGTCTGTCAACGTGTGTAGC -3′	127
CrTUB	5′- GTTGCATCGTTAGCGTGGACG -3′ 5′- GCAGCAGCCAATGTTCAGACT -3′	170
CrERF	5′- AGCCAGGCTCGCTGCAACTTCC -3′ 5′- GGA AGT TGC AGC GAG CCT GGC T -3′	108
CrATG8	5′- TCCCGATATCGACAAGAAG -3′ 5′- TGCGGATGACGTACACAAAT -3′	75