cell extracts were cleared by a second centrifugation and snap frozen in small aliquots at 80uC. In vitro end joining was measured with the pSP65 plasmid after linearization with Sal I. End-joining reactions were performed in 20 mM HEPES-KOH, pH 7.5), 10 mM MgCl2, 80 mM KCl, 1 mM ATP, 1 mM DTT, 50 ng of substrate DNA and 0.52 mg of whole cell extract in a final volume of 20 ml at 25uC for 1 h. Reactions were terminated by adding 2 ml of 5% SDS, 2 ml of 0.5 M EDTA and 1 mg of protease and incubating for 30 min at 37uC. One half of the reaction was loaded on a 0.7% agarose gel and run at 45 V for 4.5 h. Gels were stained with SYBR-Gold and scanned using the Typhoon. Supporting Information 2loxP Cdc9 cells after treatment with 4HT for the indicated periods of time, or when left untreated. A mouse monoclonal antibody against human LIG3 that recognizes the chicken LIG3 was used. GAPDH is a loading control. Western blot analysis of LIG3 and RAD51 proteins in wt DT40 cells treated with 10 mg/ml cycloheximide for the indicated periods of time. The treatment is toxic, interrupts cell growth and induces cell death starting at 4 h. Therefore results for up to 8 h of treatment are shown. In vitro DNA end joining of SalI-linearized pSP65 plasmid using 1 mg whole cell extracts of the LIG32/2loxPCdc9 mutant, prepared from untreated cultures, or cultures treated with 4HT for the indicated periods of time. The linearized input substrate plasmid 22431203 and the products generated by end joining are indicated. In vitro DNA end joining of SalI-linearized pSP65 plasmid using increasing amounts of whole cell extracts prepared from wt and LIG32/2loxP cells after treatment with 4HT for 2 d. The end joining activity loss of extracts prepared after 2 d treatment with 4HT can be rescued by the addition of 5 ng purified LIG3b, whereas end joining activity of extracts from wt cells is only slightly enhanced. The linearized input substrate plasmid and the products generated by end joining are indicated. DNA ligase activity measured with oligo/poly substrates using whole cell extracts from LIG32/2loxP cells at different times after incubation with 4HT. The graph shows the decrease in total DNA ligase activity, which in this case reflects the reduction in LIG3 levels. Results show the mean of three experiments. Colony Formation Assay Appropriate numbers of DT40 cells set in a manner allowing the accurate counting of the resulting colonies under the different conditions were seeded in medium containing 1.5% methylcellulose and incubated in 60 mm perti dishes for 1014 d before counting. Purification of LIG3b Recombinant human DNA ligase IIIb was purified from bacteria as previously described. Ligase Activity Assay For substrate preparation, an amount 
of 5 mg 16483784 of oligo16 was radioactively labeled using 5 ml of c-32P-ATP and 10 U of T4 polynucleotide kinase. The reaction was incubated at 37uC for 30 min. Labeled oligos were purified on QIAquickH columns. The labeled oligonucleotides were mixed with an 193022-04-7 site equimolar amount of polydA, incubated at 90uC for 10 min. and then slowly cooled to room temperature. Ligation reaction mixtures contained 60 mM Tris-HCl, 10 mM MgCl2, 5 mM DTT, and 1 mM ATP, 50 mg/ml nuclease-free bovine serum albumin and 0,52,5 mg of whole-cell extract and were incubated at 16uC for 60 min. Reactions were stopped with 5 ml EDTA. An aliquot was heated for 5 min at 95uC in 65% formamide prior to loading onto a 10% acrylamide gel. After electrophoresis for 1.5 h at 30
