Table 3. PCR primers used in this study.

Primers	Primer sequence
Degenerate primers
SeTre-1-F1	5′-AGYGGYTGGGAYTTCTC-3′
SeTre-1-F2	5′-TGGATYATBGAAGGTCT-3′
SeTre-1-R1	5′-GCCADGCGTTRGGGAAGTCC-3′
SeTre-1-R2	5′-CGCRTCRTAYTTCTCRAACAT-3′
For cDNA cloning
5-SeTre-1-1	5′-CACTATATTCGGATCGACAG-3′
5-SeTre-1-2	5′-GGAGCCAGGTTAGATGGGT-3′
3-SeTre-1-1	5′-CACACCAGATACATCATACC-3′
3-SeTre-1-2	5′-GGAATCACCGGGATGCTG-3′
For real-time PCR
QSeTre-1-F	5′-ATTCGCCAGAAACATCACCAAC-3′
QSeTre-1-R	5′-TTCCACTTATCAGCAGACCTCC-3′
QSeTre-2-F	5′-GGACTCTTGGGTTGATGGTGT-3′
QSeTre-2-R	5′-AGGCTTCTCAGTTCCGTGTAGG-3′
QActin-F	5′-TGCGTGACATCAAGGAGAAGC-3′
QActin-R	5′-CCATACCCAAGAAGGAAGGCT-3′
QG-6-P-I-F
eG-6-P-I-R
QUAP-F	5′-AGCAGACGGCAGACTAACTTTC-3′
QUAP-R	5′-GGACTCCTTCGTGGTCAACATAA-3′
QCHSA-F	5′-TAAGGCAAAGATTCGTCACAGG-3′
QCHSA-R	5′-CAGGGTCAGCAGATAGGTGTTC-3′
QCHSB-F	5′-CGCTGAGTCTTGTTGGTCCTGT-3′
QCHSB-R	5′-TCCACGCTACCTCTTTCCCTA-3′
For dsRNA synthesis
dsSeTre-1-F	5′-ACCAGGAACCGTCAGTAG-3′
dsSeTre-1-R	5′-GCAACCATAGCTGTCAACA-3′
dsSeTre-2-F	5′-GCCAGGACAGGTTCACATC-3′
dsSeTre-2-R	5′- GCTTCACCATCGGAATTAGG-3′
GFP-F	5′-AAGGGCGAGGAGCTGTTCACCG-3′
GFP-R	5′-CAGCAGGACCATGTGATCGCGC-3′

F: forward, R: reverse.