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. Author manuscript; available in PMC: 2013 May 1.
Published in final edited form as: DNA Repair (Amst). 2012 Apr 6;11(5):488–501. doi: 10.1016/j.dnarep.2012.02.004

Table 1. Cell lines used in this and the previous study.

The primary GM00739 fibroblast line derived from patient CS1AN was obtained from the Coriell Institute and transformed with retroviral hTERT [3]. UVSS1KO fibroblasts derived from patient UVSS1KO and transformed with a replication-defective SV40 [13] were the kind gift of Kiyoji Tanaka (Osaka University). EGFP, enhanced green fluorescent protein; hyg, hygromycin resistance; neo, neomycin resistance; fusion, CSB-PGBD3 fusion protein. Puromycin-resistant cells express untagged proteins from the bicistronic vector pIRESpuro (Clontech); hygromycin-resistant cells express FLAG-HA tagged proteins or the FLAG-HA tag alone; neomycin-resistant cells express FLAG-tagged proteins or the FLAG tag alone. Hyphens indicate transformation protocol for cell lines, antibiotic selection for transfection of genes and tags. The microarray experiments (Table S1) were performed using singly-transfected CSB-hyg and fusion-hyg pools, and a doubly-transfected CSB-hyg + fusion-neo line, all normalized for consistency to hyg alone. See Materials and methods for details.

Cell line Source Use in this study
CS1AN-hTERT Newman et al. [3]
CS1AN-hTERT + eGFP-puro Newman et al. [3] Table 4
CS1AN-hTERT + CSB-puro Newman et al. [3] Table 4
UVSS1KO-SV40 + hyg this study Fig. 2A, Tables 4 and S1
UVSS1KO-SV40 + fusion-hyg this study Fig. 2A, Tables 4 and S1
UVSS1KO-SV40 + CSB-hyg this study Fig. 2A, Tables 4 and S1
UVSS1KO-SV40 + hyg + neo this study Fig. 2B,C
UVSS1KO-SV40 + hyg + fusion-neo this study Fig. 2B,C
UVSS1KO-SV40 + fusion-hyg + neo this study Fig. 2B,C
UVSS1KO-SV40 + CSB-hyg + neo this study Fig. 2B,C
UVSS1KO-SV40 + CSB-hyg + fusion-neo this study Fig. 2B,C, Tables 4 and S1