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. 2014 Oct 8;5:504. doi: 10.3389/fpls.2014.00504

Table 1.

Primer sequences and amplification conditions for DcMADS3, DcMADS5, DcAOX2a, DcAOX2b, and DcCHS2.

Target NCBI number Marker type Forward primer Reverse primer Annealing temperature Fragments* detected in the
yel—mutant cola—mutant
DcMADS3 AJ271149 EST GTGTGATGCTAAGGTTTCG GATCCTGCTCCGCCATG 54 1500 bp
DcMADS5 AJ271151 CAPS** GGGCACAAAGGAGCTTGAGG AGAGCATCCACCCTGGAATG 50 605 bp 770 bp
DcAOX2a EU286575 EST TGCTGCATCTGAGGTCTCTCC CCAATCAATTCTACACAACAACC 55 1900 bp
DcAOX2b EU286576 EST TGCATGCGTCCTTCCTTATTTTTC AGCTTTGGTGACAGTATGTATAGG 55 1400 bp
DcCHS2 D16255 EST CTCAAGGAGAAGTTTAGGCGGATG ATGAGGCCATGTACTCGCAGAAA 56 850 bp 900 bp
*

Only polymorphic fragments were summarized. Fragments non-polymorphic between yel- and cola-parent were not mentioned.

**

The polymorphism was obtained after cleavage of the genomic DNA with Alu I to generate a CAPS (Cleaved Amplified Polymorphic Sequence) marker.