Orters were used to assess Kaiso’s regulation of the cyclin D1 promoter via the KBS and methylated CpG sites. Table 1. cyclin D1-derived oligonucleotides used in EMSA to assess Kaiso binding.Materials and Methods Cell CultureHuman MCF7 (breast carcinoma) and HCT 116 (colon carcinoma) cells were purchased from ATCC (Manassas, VA) and grown in Dulbecco’s Modified Eagles MedChemExpress Acetovanillone medium (DMEM) (Hyclone) supplemented with 4 mM L-glutamine, 100 U/ml penicillin, 100 mg/ml streptomycin (Invitrogen, Life Technologies, Grand Island, NY), 10 fetal bovine serum (Hyclone) and 0.5 mg/ ml fungizone (Invitrogen/Life Technologies). The cells were grown at 37uC and 5 CO2 in a humidified incubator. For 5azacytidine treatment, cells were incubated in 5 mM 5-azacytidine (Sigma Aldrich) in serum supplemented DMEM for 72 hours. Due to the short half-life of 5-azacytidine in solution, fresh serum supplemented DMEM with 5-azacytidine to a final concentration of 5 mM was replenished every 24 hours during the 72-hour incubation period.Probe Name Oligonucleotide Sequence# CpGs 2 3 2 3 2 3 4 3 3Electrophoretic Mobility Shift Assay (EMSA)Double-stranded oligonucleotides spanning the appropriate KBS or CpG sites in the cyclin D1 promoter were annealed, radiolabelled and purified as previously described [21]. The -1067 KBS probe (59 TTATGCCGGCTCCTGCCAGCCCCCTCACGC 39) contained the consensus Kaiso binding site (TCCTGCNA, underlined and italicized) and two CpG-dinucleotides (bold) while the +69 KBS probe (59 CTGTCGGCGCAGTAGCAGCGAGCAGCAGAG 39) contained the core KBS (CTGCNA) and three CpG-dinucleotides (bold). The cyclin D1 promoter-derived CpG oligonucleotide sequences used in this study are listed in Table 1. In brief, the CpG and +69 KBS oligonucleotides were methylated using Sss1 methyltransferase MedChemExpress 69-25-0 according to the manufacturer’s protocol (New England Biolabs NEB, Ipswich, MA). The oligonucleotides were end-labeled at 37uC for 45 minutes with [c-32P] ATP using polynucleotide kinase (NEB). Both un-methylated and methylated radiolabelled oligo21067 KBS +69 KBS CpG1 CpG2 CpG3 CpG4 CpG5 CpG6 CpG7 CpGTTATGCCGGCTCCTGCCAGCCCCCTCACGC CTGTCGGCGCAGTAGCAGCGAGCAGCAGAG GCGGGGGAGGGGGCGCGGGAGGAATTCACC CGTTCTTGGAAATGCGCCCATTCTGCCGGC TATGGGGTGTCGCCGCGCCCCAGTCACCCC GCCGCAGGGCAGGCGCGGCGCCTCAGGGAT CCCGGCGTTTGGCGCCCGCGCCCCCTCCCC GCCCCCTCCCCCTGCGCCCGCCCCCGCCCC CAGAGGGCTGTCGGCGCAGTAGCAGCGAGC GAGGGGCAGAAGAGCGCGAGGGAGCGCGGGTen oligonucleotides were synthesized from different regions of the cyclin D1 promoter and used in EMSA experiments to elucidate Kaiso binding. The CpGs are bolded while the KBSs are bolded and italicized (i.e. 21067KBS, +69KBS and CpG7). doi:10.1371/journal.pone.0050398.tKaiso Represses cyclin D1 via KBS and Me-CpG SitesTransient Transfection and Luciferase AssaysMCF7 cells were seeded at 2.56105 cells/mL into 6-well dishes and incubated for at least 12 hrs until the cells were approximately 50?0 confluent. Each well was transfected with 600 ng of reporter DNA plasmid (pGLuc-Basic, pGLuc-Basic wild type 21748CD1 or pGLuc-Basic 21748CD1 KBS (1,2) mutant), 500 ng of pRSV/b-galactosidase internal control and various amounts of effector plasmids (pcDNA3 empty, pcDNA3 human Kaiso, or pRS-Kaiso) by diluting the DNA in 150 mM NaCl and mixing gently before adding 10 equivalents (,17 ml) of ExGen500 reagent (Fermentas, Burlington, ON). The mixture was gently vortexed, and incubated without disturbing at RT for 15 minutes to allow transfection complex formation. The complexes were then a.Orters were used to assess Kaiso’s regulation of the cyclin D1 promoter via the KBS and methylated CpG sites. Table 1. cyclin D1-derived oligonucleotides used in EMSA to assess Kaiso binding.Materials and Methods Cell CultureHuman MCF7 (breast carcinoma) and HCT 116 (colon carcinoma) cells were purchased from ATCC (Manassas, VA) and grown in Dulbecco’s Modified Eagles medium (DMEM) (Hyclone) supplemented with 4 mM L-glutamine, 100 U/ml penicillin, 100 mg/ml streptomycin (Invitrogen, Life Technologies, Grand Island, NY), 10 fetal bovine serum (Hyclone) and 0.5 mg/ ml fungizone (Invitrogen/Life Technologies). The cells were grown at 37uC and 5 CO2 in a humidified incubator. For 5azacytidine treatment, cells were incubated in 5 mM 5-azacytidine (Sigma Aldrich) in serum supplemented DMEM for 72 hours. Due to the short half-life of 5-azacytidine in solution, fresh serum supplemented DMEM with 5-azacytidine to a final concentration of 5 mM was replenished every 24 hours during the 72-hour incubation period.Probe Name Oligonucleotide Sequence# CpGs 2 3 2 3 2 3 4 3 3Electrophoretic Mobility Shift Assay (EMSA)Double-stranded oligonucleotides spanning the appropriate KBS or CpG sites in the cyclin D1 promoter were annealed, radiolabelled and purified as previously described [21]. The -1067 KBS probe (59 TTATGCCGGCTCCTGCCAGCCCCCTCACGC 39) contained the consensus Kaiso binding site (TCCTGCNA, underlined and italicized) and two CpG-dinucleotides (bold) while the +69 KBS probe (59 CTGTCGGCGCAGTAGCAGCGAGCAGCAGAG 39) contained the core KBS (CTGCNA) and three CpG-dinucleotides (bold). The cyclin D1 promoter-derived CpG oligonucleotide sequences used in this study are listed in Table 1. In brief, the CpG and +69 KBS oligonucleotides were methylated using Sss1 methyltransferase according to the manufacturer’s protocol (New England Biolabs NEB, Ipswich, MA). The oligonucleotides were end-labeled at 37uC for 45 minutes with [c-32P] ATP using polynucleotide kinase (NEB). Both un-methylated and methylated radiolabelled oligo21067 KBS +69 KBS CpG1 CpG2 CpG3 CpG4 CpG5 CpG6 CpG7 CpGTTATGCCGGCTCCTGCCAGCCCCCTCACGC CTGTCGGCGCAGTAGCAGCGAGCAGCAGAG GCGGGGGAGGGGGCGCGGGAGGAATTCACC CGTTCTTGGAAATGCGCCCATTCTGCCGGC TATGGGGTGTCGCCGCGCCCCAGTCACCCC GCCGCAGGGCAGGCGCGGCGCCTCAGGGAT CCCGGCGTTTGGCGCCCGCGCCCCCTCCCC GCCCCCTCCCCCTGCGCCCGCCCCCGCCCC CAGAGGGCTGTCGGCGCAGTAGCAGCGAGC GAGGGGCAGAAGAGCGCGAGGGAGCGCGGGTen oligonucleotides were synthesized from different regions of the cyclin D1 promoter and used in EMSA experiments to elucidate Kaiso binding. The CpGs are bolded while the KBSs are bolded and italicized (i.e. 21067KBS, +69KBS and CpG7). doi:10.1371/journal.pone.0050398.tKaiso Represses cyclin D1 via KBS and Me-CpG SitesTransient Transfection and Luciferase AssaysMCF7 cells were seeded at 2.56105 cells/mL into 6-well dishes and incubated for at least 12 hrs until the cells were approximately 50?0 confluent. Each well was transfected with 600 ng of reporter DNA plasmid (pGLuc-Basic, pGLuc-Basic wild type 21748CD1 or pGLuc-Basic 21748CD1 KBS (1,2) mutant), 500 ng of pRSV/b-galactosidase internal control and various amounts of effector plasmids (pcDNA3 empty, pcDNA3 human Kaiso, or pRS-Kaiso) by diluting the DNA in 150 mM NaCl and mixing gently before adding 10 equivalents (,17 ml) of ExGen500 reagent (Fermentas, Burlington, ON). The mixture was gently vortexed, and incubated without disturbing at RT for 15 minutes to allow transfection complex formation. The complexes were then a.
