Table 1.

Primer sequences.

No.	Sequence (5′-3′)	Orientation	Description
1	CGATCTCTTGTAGATCTGTTCTCT	Forward	RT–PCR, qRT–PCR for sgRNA3 (Fig. 1C)
2	GTCTTCCTTGCCATGTTGAGT	Reverse
3	GAAGGTGAAGGTCGGAGTC	Forward	RT–PCR, qRT–PCR for GAPDH mRNA
4	GAAGATGGTGATGGGATTTC	Reverse
5	GAGCTGGTGGCCATAGTTACGGCGCCGATC	Forward	Subcloning, PCR amplification of F1
6	GTTTCAAGAGTGCGGGAGAAAATTGATC	Reverse
7	ACGATCAATTTTCTCCCGCACTCTTGAAAC	Forward	Subcloning, PCR amplification of F2
8	CACTTTTACACTTTTTAAGCACTGTCTTTG	Reverse
9	CAAAGACAGTGCTTAAAAAGTGTAAAAGTG	Forward	Subcloning, PCR amplification of F3
10	CAAACACGGTTTAAACACCGTGTAACTATG	Reverse
11	CATAGTTACACGGTGTTTAAACCGTGTTTG	Forward	Subcloning, PCR amplification of F4
12	GACAAAACCCACTTCTCTTGTTATGACTGC	Reverse
13	GCAGTCATAACAAGAGAAGTGGGTTTTGTC	Forward	Subcloning, PCR amplification of F5
14	GCATTTTCATACAAAAAAAAGAACAAAGAC	Reverse
15	GTCTTTGTTCTTTTTTTTGTATGAAAATGC	Forward	Subcloning, PCR amplification of F6
16	TAATGTGTCACAATTACCTTCATCAAAATG	Reverse
17	AGGCATTTTGATGAAGGTAATTGTGACACATTAAAAG	Forward	Subcloning, PCR amplification of F7
18	AACTATATCTGCTGTCGTCTCAGGCAATGC	Reverse
19	CTTTTGTACTGTAAATGCATTGCCTGAGAC	Forward	Subcloning, PCR amplification of F8
20	TAAACAGGAAACTGTGGCGCGCCAGTGTTA	Reverse
21	TGTTAACAACTAACACTGGCGCGCCACAGT	Forward	Subcloning, PCR amplification of F9
22	TAAAAGGTAAACAGGAAACTGTGGATCCTC	Reverse
23	GATCGGCGCCGTAACTATGGCCACCAGCTC	Forward	PCR amplification of F10
24	ACGAGTTCTTCTGAGGATCCACAGTTTCCT	Reverse
25	AAATTCCCTCGAGGACAAGGCGTTC	Forward	PCR amplification of the N gene with KpnI and XhoI restriction sites for cloning into pBluescriptII
26	TTTTGGTACCACGTTCCCGAAGGTGTG	Reverse