Proliferation was measured by seeding 4 96well plate wells, imaging whole wells at day 0, 1, 3, and 6, and scoring images for total cells (DAPI+) and subtracting the number of Sytox orange+ (dead) cells = total live cells. Total growth: table shows mean cells/line/genotype/day and standard deviation; n = 2 and n = 3 lines per WT or KO genotype respectively. Total cells is the sum of cells in four replicate wells/line. Normalized growth: Each line was normalized to its own day 0 value. Curve Fit Parameters: each line was fit with an exponential growth curve and the mean growth constants were computed and found not significantly different. Colony Size: whole colonies were segmented using MultiWavelength Cell Scoring adjusting the size and intensity thresholds so that entire colonies were segmented by DAPI signal, rather than individual cells. Mean values for n colonies counted for each line at day 0 and day six are shown, unit is μm2. No significant differences were found between genotype at either day. Proliferation: Three randomly chosen 10x fields (mean 1473 cells/field) per line were scored for total DAPI +cells and cells positive for phosphohistone H3 (PH3) in Metamorph. No significant difference between genotypes was observed. No cells were positive for activated caspase-3 or showed pyknotic nuclei, indicating negligible levels of cell death across genotypes. All statistics Student’s t-test, 1 tail, 2 sample unequal variance.