Ials and MethodsDNA sequences of all primers used for amplification by polymerase chain reactions (PCR) and site-directed mutagenesis are described in Table S1.Cell Culture and TransfectionNalm-6 [6?0] was cultured in RPMI1640 supplemented with 10 calf 22948146 serum and 50 mM 2-mercaptoethanol at 37uC under a 5 CO2 atmosphere. Cells were transfected with DNA constructs using Nucleofector I (LONZA) according to the manufacturer’s protocol. Briefly, 26106 cells were suspended into 0.1 mL of KitT solution with supplement 1, and transfected with 2 mg of a linearized targeting vector by using Program C-05. Transfected cells were cultured for 48 h at 37uC and then the optimum numbers of the cells were seeded into 96-well plates in medium containing an appropriate drug (G418; 600 mg/mL, Puromycin; 0.5 
mg/mL, Hygromycin B; 400 mg/mL). The drugsFigure 1. Comparison of Nalm-6 (MSH-) and Nalm-6-MSH+. Western blot analysis of MSH2/MSH6 expression (A) and RT-PCR analysis of MSH2 mRNA from exon 8 to 16 (B). doi:10.1371/journal.pone.0061189.gEstablishment of Human Cell Line Nalm-6-MSH+Figure 2. The CGH array analysis of the MSH2 gene in Nalm-6 genome. Part of the chromosome 2 covering the MSH2 gene is presented. The chromosome region where one allele is deleted is boxed with black color and the region where both alleles are missed is boxed with red color. The region covering MSH2 is indicated with a red thick line. doi:10.1371/journal.pone.0061189.gE8 Fw and MSH2-E16 Rv. The neomycin-resistance gene was excised by introduction of Cre recombinase expression vector by Nucleofector I.Western BlottingThe cells were extracted with PRO-PREP (iNtRON) according to the supplier’s recommendations. The whole cell extracts were fractionated on 10 sodium dodecyl sulfate polyacrylamide gel and transferred to polyvinylidene SMER 28 difluoride membranes. The membranes were blocked with 5 non-fat milk and probed withFigure 3. Strategy for re-expression of MSH2 from the endogenous promoter by gene targeting. The MSH2 gene is located on chromosome 2 and 
the indicated allele has the region from exon 1 to exon 8 of MSH2. Region from exon 9 to 16 is deleted in both chromosomes. The synthetic exon from exon 9 to exon 16 was introduced into downstream of exon 8 by targeting. After Cre recombination, NeoR is removed, and lox71 and lox66 creates a defective lox sequence, which is no longer a target of Cre recombinase. DT-A stands for diphtheria toxin-A. doi:10.1371/journal.pone.0061189.gEstablishment of 15755315 Human Cell Line Nalm-6-MSH+either a mouse anti-MSH2 monoclonal 370-86-5 site antibody (SANTA CRUZ BIOTECHNOLOGY) or a mouse anti-MSH6 monoclonal antibody (SANTA CRUZ BIOTECHNOLOGY) overnight in 5 non-fat milk solution. After washing three times with phosphate-buffered saline containing 0.05 Tween 20, the membranes were incubated with an anti-mouse IgG conjugated to horseradish peroxidase (GE Healthcare Bio-Sciences) for 1 h. The MSH2 and MSH6 were then visualized using the Enhanced Chemiluminescence (ECL) System (GE Healthcare Bio-Sciences).HPRT Mutation AssaysCells were treated with CHAT medium, which contained 10 mM deoxycytidine, 200 mM hypoxanthine, 0.1 mM aminopterin, and 17.5 mM thymidine, to reduce the background mutant fraction and then cultured with normal medium for 7 days to permit generation of spontaneous HPRT-deficient mutants. To isolate the mutants, cells were seeded into 96-well plates at 8000 or 40000 cells/well in the presence of 0.5 mg/mL 6-thioguanine. The plates were incubated fo.Ials and MethodsDNA sequences of all primers used for amplification by polymerase chain reactions (PCR) and site-directed mutagenesis are described in Table S1.Cell Culture and TransfectionNalm-6 [6?0] was cultured in RPMI1640 supplemented with 10 calf 22948146 serum and 50 mM 2-mercaptoethanol at 37uC under a 5 CO2 atmosphere. Cells were transfected with DNA constructs using Nucleofector I (LONZA) according to the manufacturer’s protocol. Briefly, 26106 cells were suspended into 0.1 mL of KitT solution with supplement 1, and transfected with 2 mg of a linearized targeting vector by using Program C-05. Transfected cells were cultured for 48 h at 37uC and then the optimum numbers of the cells were seeded into 96-well plates in medium containing an appropriate drug (G418; 600 mg/mL, Puromycin; 0.5 mg/mL, Hygromycin B; 400 mg/mL). The drugsFigure 1. Comparison of Nalm-6 (MSH-) and Nalm-6-MSH+. Western blot analysis of MSH2/MSH6 expression (A) and RT-PCR analysis of MSH2 mRNA from exon 8 to 16 (B). doi:10.1371/journal.pone.0061189.gEstablishment of Human Cell Line Nalm-6-MSH+Figure 2. The CGH array analysis of the MSH2 gene in Nalm-6 genome. Part of the chromosome 2 covering the MSH2 gene is presented. The chromosome region where one allele is deleted is boxed with black color and the region where both alleles are missed is boxed with red color. The region covering MSH2 is indicated with a red thick line. doi:10.1371/journal.pone.0061189.gE8 Fw and MSH2-E16 Rv. The neomycin-resistance gene was excised by introduction of Cre recombinase expression vector by Nucleofector I.Western BlottingThe cells were extracted with PRO-PREP (iNtRON) according to the supplier’s recommendations. The whole cell extracts were fractionated on 10 sodium dodecyl sulfate polyacrylamide gel and transferred to polyvinylidene difluoride membranes. The membranes were blocked with 5 non-fat milk and probed withFigure 3. Strategy for re-expression of MSH2 from the endogenous promoter by gene targeting. The MSH2 gene is located on chromosome 2 and the indicated allele has the region from exon 1 to exon 8 of MSH2. Region from exon 9 to 16 is deleted in both chromosomes. The synthetic exon from exon 9 to exon 16 was introduced into downstream of exon 8 by targeting. After Cre recombination, NeoR is removed, and lox71 and lox66 creates a defective lox sequence, which is no longer a target of Cre recombinase. DT-A stands for diphtheria toxin-A. doi:10.1371/journal.pone.0061189.gEstablishment of 15755315 Human Cell Line Nalm-6-MSH+either a mouse anti-MSH2 monoclonal antibody (SANTA CRUZ BIOTECHNOLOGY) or a mouse anti-MSH6 monoclonal antibody (SANTA CRUZ BIOTECHNOLOGY) overnight in 5 non-fat milk solution. After washing three times with phosphate-buffered saline containing 0.05 Tween 20, the membranes were incubated with an anti-mouse IgG conjugated to horseradish peroxidase (GE Healthcare Bio-Sciences) for 1 h. The MSH2 and MSH6 were then visualized using the Enhanced Chemiluminescence (ECL) System (GE Healthcare Bio-Sciences).HPRT Mutation AssaysCells were treated with CHAT medium, which contained 10 mM deoxycytidine, 200 mM hypoxanthine, 0.1 mM aminopterin, and 17.5 mM thymidine, to reduce the background mutant fraction and then cultured with normal medium for 7 days to permit generation of spontaneous HPRT-deficient mutants. To isolate the mutants, cells were seeded into 96-well plates at 8000 or 40000 cells/well in the presence of 0.5 mg/mL 6-thioguanine. The plates were incubated fo.
