Skip to main content
. 2016 Feb 9;11(2):e0148560. doi: 10.1371/journal.pone.0148560

Table 1. Primers used for plasmids construction.

Primers Primer sequence Genes
mZVF 5' ATC GTC CAA TGC TAA AAA GGG GCC CAT GGT CGG GTT CC 3' V protein of ZJ1
mZVR 5' AAC CCG ACC ATG GGC CCC TTT TTA GCA TTG GAC GAT 3'
mLVF 5' CAA TGC TAA AAA GGG GCC CAT GGT CGA GCC CCC AAG AG 3' V protein of LaSota
mLVR 5' TTG GGG GCT CGA CCA TGG GCC CCT TTT TAG CAT TGG A 3'
m9VF 5' ATC GAA TGC TAA AAA GGG GCC CAC CTC AGA GCC CTC CA 3' V protein of 9a5b
m9VR 5' GAG GGC TCT GAG GTG GGCCCC TTT TTA GCA TTC GAT 3'
p9PNF 5' GGT GAA TTC ATG GCT ACG TTC ACG GAC GCA GAG A 3' V protein of 9a5b
p9VCR 5' CAA TCC GAG TCA ATC TTG CTT ACC CTC TGT G 3'
ZJVCDF 5' A TCA GAA TTC ATG GTC GGG TTC CCA AGA AGG GCA TCA CCA AC 3' C-terminal domain of ZJ1 V
pZJVR 5' CTG ATG A GTC GAC TTA CTT ACC TTC TGT GAT AAT GCC TCC A 3'
Fla14sta1F 5' AGGGATATCGATGTCTCAGTGGTACGAACTTCAGCAGCT 3' Human STAT1α and its mutant
Fla14sta1R 5' TCATGGATCCTACTGTGTTCATCATACTGTCGAATTCTA 3'

Note: To construct V ORFs, an extra one G was inserted behind the RNA-editing site of pCI-P/ZJ1, pCI-P/LaSota and pCI-P/9a5b using primer sets mZVF/mZVR, mLVF/mLVR and m9VF/m9VR. The added extra G was boxed. To produce anti-V mouse polyclonal serum, the complete V ORF and CTD sequence were PCR-amplified from pCI-V/9a5b and pCI-V/ZJ1 constructed with primer sets p9PNF/ p9VCR and ZJVCDF/ pZJVR. Fla14sta1F/Fla14sta1R were used for PCR amplification of the complete ORFs of wt or mutated human STAT1 protein from plasmids stat1 alphap RC/CMV and stat1 alphap Y701F RC/CMV. The restriction endonuclease sites were underlined.