Skip to main content
. 2001 Jan;21(2):400–413. doi: 10.1128/MCB.21.2.400-413.2001

TABLE 1.

Effect of irradiation on CJ formation in wild-type and SCID thymic lymphoma cellsa

Cell line Expt no. Irradiation No. of Ampr No. of Camr %R IR/C
VL3-3M2 1 2,610,000 124,000 4.75
0.5 h (A) 2,740,000 248,000 9.05 1.91
LK6.2 1 154,000 615 0.40
0.5 h (B) 106,000 2,260 2.13 5.34
0.5 h (A) 247,000 4,350 1.76 4.41
LK3C 1 69,300 142 0.20
0.5 h (B) 12,300 77 0.63 3.06
VL3-3M2 2 398,000 29,600 7.4
0.5 h (B) 192,000 13,800 7.2 0.97
LK6.2 2 439,000 2,480 0.6
0.5 h (B) 9,600 225 2.3 4.15
VL3-3M2 3 1,260,000 8,140 0.65
0.5 h (B) 2,510,000 50,000 1.99 3.08
LK6.2 3 929,000 429 0.05
0.5 h (B) 121,000 964 0.80 17.25
LK8 3 1,870,000 694 0.04
0.5 h (B) 379,000 411 0.11 2.92
a

The efficiency of CJ formation was measured as percent recombination (%R) for each cell line as described in Materials and Methods. Briefly, 40 to 48 h after transient transfection with pDR42, plasmid DNA harvested from each cell line was electroporated into E. coli. The percent recombination (%R) was calculated as the ratio (×100) between the number of colonies resistant to ampicillin (Ampr) and those resistant to ampicillin plus chloramphenicol (Camr). Cell lines were treated with 100 cGy of γ-irradiation at the indicated times before (B) or after (A) transfection with pDR42. The number of cells recovered after 48 h did not vary more than twofold within each group. The effect of irradiation on the efficiency of CJ formation was calculated as the ratio of recombination frequencies of irradiated cultures to those of control cultures (IR/C). −, no irradiation.