Table 2 Primers used. Sequences of the primers used for cloning of the promoter and gene fragments, for PCR screening of the putative transgenic plants, and for Real Time quantification of transcript levels. For further details, see Methods.

B33-149 Up

ACATATTTTACTTTTGACTTT

B33-1950 Dw

GTAGTGTCACACTTACGC

B33 Up

AGTCGACAATCATTGTTTTATTTTCTCTTTC

B33 Dw

AGGATCCAAATTTTGTTGGTGCTTTGAG

Lcy-e 322 Up

AGAGCTCGGCTGTGGTCCTGCTG

Lcy-e 1085 Dw

AGGATCCTGGCAAAGATCCACCAAC

Lcy-e 574 Up

TAGGATCATCATCATCAAG

Nos-test2

CGCGTATTAAATGTATAATTG

Tub 865 Up

CTGTGAATTTAATCCCCTTG

Tub 1260 Dw

TGCGCCTGAACATGGCAGT

Tub Up

CAGACCTGAGGAAATTGGCTG

Tub Dw

TTCTTGGCATCCCACATTTGT

Ubi Up

ACAATGTCAAAGCCAAGATCCA

Ubi Dw

CGGAGACGGAGCACGAGA

AS-e Up

CCCCAATTTAGCAGACTCCG

AS-e Dw

CAACAGAAATTATATGATAATCATCGCAA

Psy1 Up

CGGTCTGCTATTGTTGCTACTCC

Psy1 Dw

CAGGAACAGGTATGTCTGGCTTC

Psy2 Up

AGCTTTAGATAGGTGGGAGGCA

Psy2 Dw

CAAGTCCATACGCATTCCTTCAA

PDS Up

AGAGACTTTGCATGCCGATTGT

PDS Dw

AAAGCATCGCCCTCAACTGT

ZDS Up

TTGCCATGTCAAAGGCCA

ZDS Dw

ACAGGCACTCCGACCAATTT

CrtIso Up

TTGGCAGCAGTAGGACGTAAAC

CrtIso Dw

TCCCTTCCTTTTCATGTGGAA

Lcy-e Up

GCCAAAATGGATGTGGCAG

Lcy-e Dw

CAATGTTGCACCAGTAGGATCAG

Lut1 Up

CGTTCTCCGCCCAAAAAAC

Lut1 Dw

TTGGCCTAAAGTAAGTGACCTGG

Lcy-b Up

AATGGGTGGTCCACTTCCAGTA

Lcy-b Dw

GGATGGATGAACCATGCCAG

Chy1 Up

CTTGGCCCAAAACCCACTT

Chy1 Dw

CCTCAAATTGAGGTTTCAGCTTCT

Chy2 Up

TTTTGCTGTCTCGAAGAAAGCC

Chy2 Dw

AGCCAACAGGCAGCTAAACTCT

ZEP Up

TCATGAATGCTGGCTGCATC

ZEP Dw

TGCTGCAAAGTCATGCGG