Table 3. Primers used in this study.

Primer name	Strand orientation	Sequence(5′→3′)	Application
GADPH	Forward	CATTGAAGGTCTGATGACCACTGT	Quantitative RT PCR
	Reverse	CAGAGGGTCCATCCACTGTCTT
	Probe	CACGCCACCATTGCCACCCA
Actin	Forward	GGTGCACTGGCGATATTGG
	Reverse	CTTGGGTCTTGACAGCAATGC
	Probe	AACCCCTTGGTCTGCCATGATAGCCTT
HaTry1 (EU982841)	Forward	GGTGCACTGGCGATATTGG
	Reverse	CTTGGGTCTTGACAGCAATGC
	Probe	AACCCCTTGGTCTGCCATGATAGCCTT
HaTry2 (EU325549)	Forward	GCCCCAAGGCTTCCAGAT
	Reverse	CAGACGAAGTACCCCATCCA
	Probe	CCCGATGGCTTGCCAGTTGTTCA
HaTry3 (EU325548)	Forward	GGATTCGGAACTTGCAATGGT
	Reverse	CGAACTGCTGGCCATTGTC
	Probe	CCGGCAGTGCTCTGACCCGC
HaTry4 (AY437836)	Forward	CCAGCTATGTGCTGCTCGTTAC
	Reverse	CGCAGATAATGTTCTCAGTCACAA
	Probe	TGACCCTGCCATGGCCCCA
HaTryR (KF791044)	Forward	GGCTCCCATGGCTATGAG
	Reverse	CGTCAGTGAGACACTCCTGGAAG
	Probe	AACGCCCTGGTCGGAATCTCTTCCT
5′-RACE-GSP-outer	Reverse	AATGTCGTTGGAGCGAGGGGT	RACE PCR
5′-RACE-GSP-inner	Reverse	CCTACCACGACTCCTCCAGCCAA
3′-RACE-GSP-outer	Forward	TGCTGTACCTGCCTCCTGTCAA
3′-RACE-GSP-inner	Forward	ACTCCGAAGATGTTACCGTTTC
dsRNA-GFP	Forward	TAATACGACTCACTATAGTCCCAACACTTGTCACTAC	dsRNA amplification
	Reverse	TAATACGACTCACTATAGAAACTCAAGAAGGACCATG
dsRNA-HaTryR	Forward	TAATACGACTCACTATAGTTCATTCTCGCCATCTTG
	Reverse	TAATACGACTCACTATAGCATCTTCGGAGTCATCGTA
CTD039 SP1	Reverse	TTCAAGAGCACTTAGAGACTTT	Promoter cloning
CTD039 SP2	Reverse	TTGAACATCACGCTTAACACTA
CTD039 SP3	Reverse	AGGGCTTTCAACAGATACTTC
activity -Bgl II	Forward	ATAGATCTAGATAATTTGTACGTGCCAGATTGTC	Construction of luciferase reporter plasmids
activity –Nhe I	Reverse	ATGCTAGCGTTTCAACTGACCCACTGAA
Genetic linkage-F	Forward	AGATAATTTGTACGTGCCAGATTGTC	Genetic linkage analysis
Genetic linkage-R	Reverse	AAGATGGCGAGTAAGAAGTACGCAA