Table 1.

Primers used in the study.

Primer name	Sequence (5′–3′)
tps46 fragment clone
RiTPS46-forward	TCAggtaccactagtCTACACGAAATGAAGCCATA
RiTPS46-reverse	CATggatccgagctcAGTTCCAGGTGTTCCTCTAT
tps46 gene clone
OeTPS46-forward	CATGTCATCGACACCTGCA
OeTPS46-reverse	TTAAATGCTATATGGCTCAACG
qRT-PCR
TPS46-forward	TGAAGAGGCACTAGGTCCAAAC
TPS46-reverse	CCATCCCAACTAAAGAAGCACA
EF1α-forward	AGACGCACATCAACATCG
EF1α-reverse	GAACTTCCACAGGGCAATA
Race-PCR
TPS46-3′GSP1	CACACGATGGTGGAAAGAGCTTAACGTTG
TPS46-3′GSP2	GACAGGAGCATGCTCGGAGCCCCATTA
TPS46-5′GSP1	CAAGCATCATGCTCTCCTCGGTTGTAGC
TPS46-5′GSP2	TGGACCTAGTGCCTCTTCAAATGAATCAA

The restriction sites used for clone are underlined and shown in bold.