The ability of DEPN-8+1.5% bovine SP-B/ C to resist inhibition by PLA2, albumin or LPC to an equal or greater extent than CLSE in these prior studies is impressive

April 20, 2017

tected, as expected, in LIG42/2 cells 8 h after IR, but this repair defect is not further enhanced in the double mutant LIG12/2LIG42/2. The above observations in aggregate suggest that independently of the dose of radiation applied, LIG3, as sole ligase, supports processing of DSBs in D-NHEJ deficient cells and that LIG1 is not required for this function. Conditional Down-regulation of LIG3 Reveals the Function of LIG1 in Alternative NHEJ Genetic studies on the roles and 16483784 the interplay between LIG3 and LIG1 in DSB repair were hampered by the lethality of LIG32/2 cells. To partly overcome this limitation we generated a conditional mutant, LIG32/2loxP. This mutant carries one null LIG3 allele and one conditional allele with loxP sites Chlorphenoxamine custom synthesis inserted between several exons to allow their controlled excision by Cre recombinase. In the DT40 cells used in the present work, Cre is constitutively expressed in the cytoplasm but translocates into the nucleus after treatment with 4-hydroxytamoxifen . LIG32/2loxP cells process DSBs with kinetics indistinguishable from that of wt cells. As a result of single allele expression, LIG3 mRNA is in LIG32/2loxP cells 50% reduced. We conclude that the associated reduction in LIG3 protein levels leaves unchanged the processing potential of these cells, even at radiation doses producing large numbers of DSBs. To examine the effect on DSB processing of a further reduction in LIG3 protein level, we analyzed DSB repair kinetics in LIG32/ 2loxP cells exposed to radiation after incubation with 4HT. In wt DT40, long-term treatment with 4HT leaves unchanged the distribution of cells throughout the cell cycle, their proliferative capacity, and their ability to repair DSBs. In LIG32/2loxP cells, on the other hand, and as a direct consequence of excision of the conditional allele, 4HT causes a rapid reduction in LIG3 mRNA to less than 10% of the controls within 6 h and to practically undetectable levels 24 h later. The reduction in mRNA causes a reduction in LIG3 protein. Notably, this reduction in protein levels is much slower than the reduction in mRNA and becomes detectable only 3 d after 4HT treatment. Depletion of LIG3 is lethal in DT40 DNA Ligases in Alternative NHEJ and causes apoptosis starting 4 days after treatment with 4HT. As protein level should determine protein function in DSB repair, we studied in greater detail the significance of the slow kinetics of LIG3 protein decay shown in Fig. 3C. Since apoptosis in 4HT treated LIG32/2loxP compromises reliable analysis of protein levels after long incubation times, we analyzed LIG3 levels in LIG32/2loxPCdc9 cells. In this mutant, treatment with 4HT deletes LIG3 without inducing cell lethality because mitochondria function is rescued by the yeast LIG1 homolog, Cdc9. Treatment of these cells with 4HT causes a clear reduction in LIG3 16483784 level, which further validates our conditional knockout system. However, here again the LIG3 polypeptide remains detectable even 10 d after 4HT treatment further documenting its unusual stability in DT40. The stability of LIG3 is also indicated by the lack of any reduction 8 h after treatment with cycloheximide; longer incubations caused apoptosis and were therefore excluded from the analysis. On the other hand, the same treatment shows clear reduction in Rad51 levels, similar to that reported earlier. Thus, the LIG3 protein appears to display an unusual and hitherto not explainable stability in DT40. For the interpretation of the DSB repair r