Figure 2
Figure 2. Stable expression of FANCA in EUFA867 lymphoblasts partially corrects the phenotype of this cell line. (A) EUFA867 lymphoblasts stably expressing wild-type FANCA are still hypersensitive to growth inhibition by mitomycin C. FANCA-deficient HSC72 and EUFA867 lymphoblasts were transduced with SF91-FANCA. Viable cells were measured with the Cell Titer 96 Proliferation Assay. The data represent the percentage growth compared with untreated cells and show 1 representative result of 3 independent experiments with standard deviations. (B) EUFA867 lymphoblasts stably expressing wild-type FANCA show melphalan-induced G2 arrest. (C) EUFA867 lymphoblasts stably expressing wild-type FANCA have reduced FANCD2 monoubiquitination. Cells were treated with either 2 mM HU or 240 nM MMC for 16 hours or left untreated. Total lysates were immunoblotted for FANCM, FANCD2, and FANCA.

Stable expression of FANCA in EUFA867 lymphoblasts partially corrects the phenotype of this cell line. (A) EUFA867 lymphoblasts stably expressing wild-type FANCA are still hypersensitive to growth inhibition by mitomycin C. FANCA-deficient HSC72 and EUFA867 lymphoblasts were transduced with SF91-FANCA. Viable cells were measured with the Cell Titer 96 Proliferation Assay. The data represent the percentage growth compared with untreated cells and show 1 representative result of 3 independent experiments with standard deviations. (B) EUFA867 lymphoblasts stably expressing wild-type FANCA show melphalan-induced G2 arrest. (C) EUFA867 lymphoblasts stably expressing wild-type FANCA have reduced FANCD2 monoubiquitination. Cells were treated with either 2 mM HU or 240 nM MMC for 16 hours or left untreated. Total lysates were immunoblotted for FANCM, FANCD2, and FANCA.

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