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. 2018 Dec 21;47(5):2402–2424. doi: 10.1093/nar/gky1279

Figure 2.

Figure 2.

LIG1 is required for 17p sister chromatid telomere fusions. (A) Fusion amplicons derived from 17p or 21q TALEN (TLN) or control (0 DNA) -transfected unsynchronized or G2-arrested L1−/fx:Cre were visualized by Southern hybridization using probes specific for the 17p (upper panels) or 21q subtelomeric (lower panels) sequence. A 2.9 kb constitutive amplicon band of known sequence identity is also detected with the 21q probe, but excluded from all fusion amplicon analyses. (B) Summary of 17p telomere fusion frequency (fusions/ng DNA input x10−2) data from seven independent 17p TLN and control (C) transfection experiments in unsynchronized (U) and G2-arrested (G2) L3−/−:L4−/-and L1−/fx:Cre cells displayed as mean values with 95% confidence intervals with one-tailed paired T-tests or Mann–Whitney U-tests, as appropriate. (C) Box and whiskers representation of 17p telomere fusion frequency data presented in (b) as a pooled data comparison of all 17p TALEN-transfected L3−/−:L4−/− (grey) samples with all MeOH-treated L1−/fx:Cre (black) samples and compared by two-tailed Mann–Whitney U-test. (D) Summary of 21q telomere fusion frequency (fusions/ng DNA input ×10−2) data from 3 independent 21q TLN and control (C) transfection experiments in G2-arrested L3−/−:L4−/-and L1−/fx:Cre cells displayed as mean values with standard deviation and one-tailed paired T-tests or Mann–Whitney U-tests, as appropriate. (E) Southern hybridization images of G2-arrested WT 17p (upper panel) and 21q (lower panel) fusion amplicons generated as in (a). Untransfected (t0) and control (GFP) transfections are included for comparison with 17p and 21q TLN-transfected samples.