TABLE 1

Oligonucleotides used in this study

Oligonucleotide Sequence (5′-3′) Purpose
2B6(-2253)F TATGAATGAGAACgcGTGATATTCACT Promoter cloning
2B6(+16)R GGACGCTGAGTTagATctTCCTGGTCTG (Mismatches in lowercase)
TQ-CYP2B6FOR GCTGAACTTGTTCTACCAGACTTTTTC Quantitative PCR
TQ-CYP2B6REV GAAAGTATTTCAAGAAGCCAGAGAAGAG
CYP2B6 MGB-probe FAM-TGTATTCGGCCAGCTGT-MGBNFQa
seqCYP2B6-P1F ACAATACCTCACTAAGAGTG Promoter sequencing
seqCYP2B6-P2F GTCTCAGTTTCTGTCTCCTTC
seqCYP2B6-P3F TGAACATGCACTACCACCA
seqCYP2B6-P4R ATCCTTGCATGTGTATGAGC
seqCYP2B6-P5R TGAACCAGGAGTAGCAAGAG
2B6-82MTF GGGGAATGGATGAAATTTCATAACAGGGTGCAGAGGC In vitro mutagenesis
2B6-82MTR GCCTCTGCACCCTGTTATGAAATTTCATCCATTCCCC
2B6-750MTF ATCACGCCCGGCTAATTTTTGT
2B6-750MTR ACAAAAATTAGCCGGGCGTGAT
2B6-801MTF GGTTCAAGTGATTCTCTTTCCTCAGCCTCCCGAG
2B6-801MTR CTCGGGAGGCTGAGGAAAGAGAATCACTTGAACC
2B6-1848MTF GTAAAGCACTTCAAGCCTCCCCATCG
2B6-1848MTR CGATGGGGAGGCTTGAAGTGCTTTAC
2B6(-3010)F GAAAGAGACTGGCTGAATGGA Genotyping -2320T→C
2B6(-1894)R TATTGTTGCCATCCCCATTT
2B6cDNA(41)R CCTGTGAGGAGTGCAAGGAAGAGG Primer extension CYP2B6
2B6cDNA(521)R GATGGAGCAGATGATGTTGGCGGTAA RACE primer CYP2B6
luci(350)R CACGGTAGGCTGCGAAATGCCCATA RACE primer Luciferase
luci(220)R AGCTTCTGCCAACCGAACGGACATTT RACE nested primer Luciferase
2B6EMSA1 sense/antisense gatccTGGATGAAATTTTATAACAGGGTGCa -94 to -70 bp EMSA (WT)
gatctGCACCCTGTTATAAAATTTCATCCAg
2B6EMSA2 sense/antisense gatccTGGATGAAATTTCATAACAGGGTGCa -94 to -70 bp EMSA (-82C)
gatctGCACCCTGTTATGAAATTTCATCCAg
2B6EMSA3 sense/antisense gatccCAGGGTCAGGATAAAAGGCCCAGTTa -64 to -40 bp EMSA
gatctAACTGGGCCTTTTATCCTGACCCTGg
  • a FAM, 5-carboxyfluorescein; MGB, minor groove binder; NFQ, nonfluorescent quencher.