Table 1.

Oligo sequences used in this study

Primers Forward (5′-3′) Reverse (5′-3′) 
TLR9 CGTCTTGAAGGCCTGGTGTTGA CTGGAAGGCCTTGGTTTTAGTGA 
β2Microglobulin TGCTGTCTCCATGTTTGATGTATCT TCTCTGCTCCCCACCTCTAAGT 
HPV16E1 CATAGAGATGCAGTACAGG CTCACCCCGTATAACTC 
HPV16E6 CCCACAGGAGCGACCCAGAAAGTT CCCATCTCTATATACTATGCATAAATCCC 
HPV16E7 As previously described (Mansour et al., 2007)  
NF-κB for ChIP   
Site A TGGGTCTGTACCTGTGTGTGCA TTCATTCCCTCCATCCACCTC 
Site B TGGATGGCCCTGTTGAGAGGG TAGCCCCTGGGCATTCTCCTG 
Site C CTGGAGAGCACTCAGGGGAAC GTCACACTAGGTCCCTCCTC 
Site D AGGCCCTGCAGAACTCTGGAG TCAGGCAGAGAGCAGGGAGA 
Cloning   
Site B CCGCTAGCAGATCTGGGGTGGGAGGTTT CTCGAGCCCCTGCTTGCAGTGATCGTG 
Mutations TLR9 promoter of NF-κB sites   
Site A NFAF: AAGGGACTCTGGGCCCTCATCAGGCTTG NFAR: CAAGCCTGATGAGGGCCCAGAGTCCCTT 
Site B NFBF: GAGACTTGGGGACTCGGTCAGGCAGAGGGA NFBR: TCCCTCTGCCTGACCGAGTCCCCAAGTCTC 
Site C NFCF: ACA/GCG/GGT/GGA/CTT/GTC/CAT/AGG/GCC/TT NFCR: AAGGCCCTATGGACAAGTCCACCCGCTGT 
Site D As previously described (Fathallah et al.)  
ERα site biotinylateda TCAGGCAGAGGTTTCAGCACATC GATGTGCTGAAACCTCTGCCTGA 
NF-κB minimal promoter sites, annealing primers CCGCTAGCGAGTTTCTCGAGCC GGCGATCGCTCAAAGAGCTCGG 
siRNA   
HPV16E6E7 UCCAUAUGCUGUAUGUGAU  
HPV16E7 GCACACACGUAGACAUUCG  
IKKα GCAGGCUCUUUCAGGGACA  
IKKβ GGUGGAAGAGGUGGUGAGC  
NF-κB As previously described (Hasan et al., 2005)  
Scramble CGAAUGUCUACGUGUGUGC  
Primers Forward (5′-3′) Reverse (5′-3′) 
TLR9 CGTCTTGAAGGCCTGGTGTTGA CTGGAAGGCCTTGGTTTTAGTGA 
β2Microglobulin TGCTGTCTCCATGTTTGATGTATCT TCTCTGCTCCCCACCTCTAAGT 
HPV16E1 CATAGAGATGCAGTACAGG CTCACCCCGTATAACTC 
HPV16E6 CCCACAGGAGCGACCCAGAAAGTT CCCATCTCTATATACTATGCATAAATCCC 
HPV16E7 As previously described (Mansour et al., 2007)  
NF-κB for ChIP   
Site A TGGGTCTGTACCTGTGTGTGCA TTCATTCCCTCCATCCACCTC 
Site B TGGATGGCCCTGTTGAGAGGG TAGCCCCTGGGCATTCTCCTG 
Site C CTGGAGAGCACTCAGGGGAAC GTCACACTAGGTCCCTCCTC 
Site D AGGCCCTGCAGAACTCTGGAG TCAGGCAGAGAGCAGGGAGA 
Cloning   
Site B CCGCTAGCAGATCTGGGGTGGGAGGTTT CTCGAGCCCCTGCTTGCAGTGATCGTG 
Mutations TLR9 promoter of NF-κB sites   
Site A NFAF: AAGGGACTCTGGGCCCTCATCAGGCTTG NFAR: CAAGCCTGATGAGGGCCCAGAGTCCCTT 
Site B NFBF: GAGACTTGGGGACTCGGTCAGGCAGAGGGA NFBR: TCCCTCTGCCTGACCGAGTCCCCAAGTCTC 
Site C NFCF: ACA/GCG/GGT/GGA/CTT/GTC/CAT/AGG/GCC/TT NFCR: AAGGCCCTATGGACAAGTCCACCCGCTGT 
Site D As previously described (Fathallah et al.)  
ERα site biotinylateda TCAGGCAGAGGTTTCAGCACATC GATGTGCTGAAACCTCTGCCTGA 
NF-κB minimal promoter sites, annealing primers CCGCTAGCGAGTTTCTCGAGCC GGCGATCGCTCAAAGAGCTCGG 
siRNA   
HPV16E6E7 UCCAUAUGCUGUAUGUGAU  
HPV16E7 GCACACACGUAGACAUUCG  
IKKα GCAGGCUCUUUCAGGGACA  
IKKβ GGUGGAAGAGGUGGUGAGC  
NF-κB As previously described (Hasan et al., 2005)  
Scramble CGAAUGUCUACGUGUGUGC  
a

Other biotin-labeled oligo probes were generated using site B forward WT or mutated biotinylated primers and respective nonbiotinylated reverse primers. Probe DNA was amplified using the TLR9 promoter plasmid as a template.

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