Processing of DNA for nonhomologous end-joining by cell-free extract
2005; Springer Nature; Volume: 24; Issue: 4 Linguagem: Inglês
10.1038/sj.emboj.7600563
ISSN1460-2075
Autores Tópico(s)Cancer therapeutics and mechanisms
ResumoArticle3 February 2005free access Processing of DNA for nonhomologous end-joining by cell-free extract Joe Budman Joe Budman Departments of Medicine and Biochemistry, Stanford University, Stanford, CA, USA Search for more papers by this author Gilbert Chu Corresponding Author Gilbert Chu Search for more papers by this author Joe Budman Joe Budman Departments of Medicine and Biochemistry, Stanford University, Stanford, CA, USA Search for more papers by this author Gilbert Chu Corresponding Author Gilbert Chu Search for more papers by this author Author Information Joe Budman1 and Gilbert Chu 1Departments of Medicine and Biochemistry, Stanford University, Stanford, CA, USA *Corresponding author. Departments of Medicine and Biochemistry, Stanford University, CCSR Building Room 1145, 269 Campus Drive, Stanford, CA 94305-5151, USA. Tel.: +1 650 725 6442; Fax: +1 650 736 2282; E-mail: [email protected] The EMBO Journal (2005)24:849-860https://doi.org/10.1038/sj.emboj.7600563 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions Figures & Info In mammalian cells, nonhomologous end-joining (NHEJ) repairs DNA double-strand breaks created by ionizing radiation and V(D)J recombination. We have developed a cell-free system capable of processing and joining noncompatible DNA ends. The system had key features of NHEJ in vivo, including dependence on Ku, DNA-PKcs, and XRCC4/Ligase4. The NHEJ reaction had striking properties. Processing of noncompatible ends involved polymerase and nuclease activities that often stabilized the alignment of opposing ends by base pairing. To achieve this, polymerase activity efficiently synthesized DNA across discontinuities in the template strand, and nuclease activity removed a limited number of nucleotides back to regions of microhomology. Processing was suppressed for DNA ends that could be ligated directly, biasing the reaction to preserve DNA sequence and maintain genomic integrity. DNA sequence internal to the ends influenced the spectrum of processing events for noncompatible ends. Furthermore, internal DNA sequence strongly influenced joining efficiency, even in the absence of processing. These results support a model in which DNA-PKcs plays a central role in regulating the processing of ends for NHEJ. Introduction Nonhomologous end-joining (NHEJ) is important for repairing DNA double-strand breaks produced by ionizing radiation. Furthermore, NHEJ is absolutely required for resolving double-strand breaks during V(D)J recombination, the pathway that generates immunological diversity. While the error-free pathway of homologous recombination restores broken DNA to its original sequence, the error-prone pathway of NHEJ often processes the DNA by adding or deleting nucleotides before joining the ends. Processing occurs after ionizing radiation, which produces chemically modified DNA ends that are not directly ligatable. Furthermore, processing contributes to the immunological diversity generated by V(D)J recombination. NHEJ in vivo requires Ku, DNA-PKcs, Artemis, and XRCC4/Ligase4. Ku is a heterodimer of 70 and 80 kDa that binds to DNA ends (Smider et al, 1994; Taccioli et al, 1994). DNA-PKcs, the catalytic subunit of DNA-dependent protein kinase, is a 465 kDa ser/thr kinase in the phosphoinositol 3-kinase (PI3K) superfamily (Hartley et al, 1995). DNA-PKcs binds to DNA ends upon recruitment by Ku (Hammarsten and Chu, 1998), mediates synapsis of the ends, and then undergoes activation of its kinase (DeFazio et al, 2002). Kinase activity is required for NHEJ, but its function remains obscure. Artemis exists in a complex with DNA-PKcs and has nuclease activity (Ma et al, 2002). XRCC4/Ligase4 executes the final step of ligation (Grawunder et al, 1997). Cell-free systems for NHEJ have been reported previously, but each system was unable to reproduce all of the key characteristics observed in vivo. Some systems were independent of DNA-PKcs (Boe et al, 1995; Johnson and Fairman, 1996; Mason et al, 1996). A subsequent end-joining system was only partially dependent on Ku (Feldmann et al, 2000). Extracts from wild-type K1 hamster cells joined compatible and noncompatible DNA ends, but extracts from Ku-deficient xrs6 hamster cells were still capable of joining ends with 14–46% of the efficiency in wild-type K1 extracts. By contrast, intact xrs6 cells have a much more severe defect. They join ends created during V(D)J recombination with less than 0.1% of wild-type efficiency (Taccioli et al, 1993). Another cell-free system yielded circularization and dimerization of linear DNA with noncompatible ends (Pospiech et al, 2001). Circularization was blocked by wortmannin, which inhibits kinases in the PI3K family. However, dimerization, which accounted for most of the joining activity, was unaffected by wortmannin or anti-Ku antibodies. Furthermore, junctions were studied for only one set of noncompatible ends, and deletion of internal DNA sequences was a rare event. A cell-free system fully dependent on Ku, DNA-PKcs, and XRCC4/Ligase4 has been established, but it was limited to the joining of compatible ends (Baumann and West, 1998). The reaction required inositol hexakisphosphate (Hanakahi et al, 2000) and polynucleotide kinase for ends with 5′-OH groups (Chappell et al, 2002). There are no reports that this system can support processing of other types of noncompatible ends. Thus, a cell-free system for the entire NHEJ reaction has remained elusive. Here, we report that human cell extract supports NHEJ of noncompatible DNA ends. To observe the processing reactions, we employed a PCR assay that enabled us to recover junctions specific for the noncompatible ends. After discovering that processing included polymerase activity, we were able to achieve high joining efficiencies by including dNTPs in the reaction. Processing also included nucleotide deletion to regions of microhomology, as observed for V(D)J recombination in vivo. Joining was highly dependent on proteins required in vivo: Ku, DNA-PKcs, and XRCC4/Ligase4. Characterization of this system led to new insights into the pathway of NHEJ. Results NHEJ is an intermolecular reaction that can be measured by quantitative PCR (qPCR) We reproduced NHEJ of compatible DNA ends as previously reported (Baumann and West, 1998). A radiolabeled DNA fragment (0.5 μg/ml) was incubated with cell extract and the DNA products were resolved by gel electrophoresis. We used DNA molecules with lengths of 2686 base pairs (bp), similar to the DNA used by Baumann and West, and 820 bp, the same length as the DNA used later in this report. Gel electrophoresis revealed that the extract joined the DNA into linear dimers, trimers, and higher order multimers, but not into circular monomers (data not shown). This result is also present in data from other groups (Baumann and West, 1998; Chen et al, 2001b). By contrast, a parallel incubation of T4 DNA ligase with the 2686 bp DNA generated products that were 75% circular monomers. We concluded that the failure to observe circular monomers in the NHEJ reaction was due to extensive binding of the DNA to proteins in the extract. Therefore, we focused on intermolecular joining in our assay for NHEJ. To study intermolecular joining, we prepared a series of DNA substrates with different ends. Since we wanted to investigate processing of ends prior to joining, it was critically important to be confident of the sequence at the DNA ends. We carefully prepared DNA substrates free of unwanted DNA contaminants, as described in Materials and methods. Sequencing of 364 junctions from the different DNA ends reported in this paper showed no evidence of contaminating DNA fragments. To measure the joining efficiency of various noncompatible ends, we developed a PCR assay (Figure 1). Although the PCR primers amplified junctions joined in a specific orientation, restriction enzyme analysis showed that the DNA fragments were joined in all possible orientations. Head-to-head joining of the same fragment to itself could potentially make a spurious contribution to our measurement of joining efficiency. To rule out this possibility, we carried out PCR with a single primer. No product was detected, consistent with the known failure of PCR to amplify long inverted repeats. Therefore, our PCR assay successfully detected joining of two well-defined DNA ends. Figure 1.Assay for NHEJ in vitro. DNA substrates were synthesized with various DNA ends attached to the same internal DNA sequences, DNA1 and DNA2. The figure shows substrates with compatible and noncompatible ends. In some cases, we synthesized DNA substrates in which the DNA ends were exchanged with respect to the internal DNA sequences, as illustrated for the noncompatible ends in the figure. Joining efficiency was measured by qPCR. Processing of the ends was analyzed after amplifying DNA junctions by PCR and sequencing individual clones. Download figure Download PowerPoint Extract supports the processing of noncompatible ends for NHEJ Cell extract supported joining of both compatible and noncompatible DNA ends (Figure 2A). ATP and Mg2+ were necessary for the joining reaction (data not shown). As a control, T4 ligase joined compatible ends but failed to join noncompatible ends. Thus, the extract actively processed noncompatible ends into a ligatable form. Figure 2.Extract supports NHEJ of noncompatible ends. (A) NHEJ is detectable by a gel-based assay. In lanes 2, 6, 10, and 14, DNA substrates with compatible or noncompatible ends were incubated with extract and dNTPs. The resulting junctions were amplified by 30 cycles of PCR, and the PCR product was resolved by gel electrophoresis. In lanes 3, 7, 11, and 15, the extract was pre-incubated for 30 min with 10 μM wortmannin (wort) to inhibit the kinase activity of DNA-PKcs. In lanes 4, 8, 12, and 16, end-joining was catalyzed by T4 DNA ligase, which joins only compatible DNA ends. (B) The NHEJ reaction requires DNA-PKcs and XRCC4, while dNTPs stimulate joining of noncompatible ends. DNA substrates with compatible or noncompatible ends were incubated with extract (+dNTPs), extract (−dNTPs), extract (+dNTPs) treated with wortmannin, or extract (+dNTPs) immunodepleted with αXRCC4 antibody (2 × 4). Joining efficiency was measured by qPCR and displayed on a log plot to account for the large variation in joining. The small arrows in place of the bottom two bars represent joining efficiency of less than 0.0001%. Download figure Download PowerPoint To test the dependence of the joining reaction on kinase activity, we added wortmannin to the extract and confirmed the loss of DNA-stimulated kinase activity (data not shown). Wortmannin strongly inhibited the joining of both compatible and noncompatible ends (Figure 2A). Thus, DNA-dependent kinase activity was required for joining both in the presence and absence of processing. To measure joining efficiency as a percentage of DNA ends joined, we employed a qPCR assay. To characterize the assay, we performed time courses of the end-joining reactions (Supplementary Figure 1). Joining of compatible and noncompatible ends reached asymptotic levels after 90 min. For the rest of our experiments, we chose to measure joining efficiency at this time point rather than an earlier time point because small errors in reaction time did not affect the results. The percentage of DNA ends joined was determined from parallel PCR amplifications of pre-formed DNA junctions (see Materials and methods). Joining of both compatible and noncompatible ends was inhibited eight- to 20-fold by immunodepletion with antibodies against Ku70, Ku80, or DNA-PKcs (data not shown). This level of inhibition was approximately equal to the degree of immunodepletion that we were able to achieve. Our failure to completely deplete extracts of Ku and DNA-PKcs may be due to the abundance of these proteins in human cells. More significantly, addition of wortmannin or immunodepletion with anti-XRCC4 antibody inhibited joining by at least 500-fold (Figure 2B). Thus, NHEJ in extract was appropriately dependent on Ku, DNA-PKcs, and XRCC4/Ligase4. NHEJ efficiency depends on the structure of the ends To determine how the structure of DNA ends influenced joining, we tested DNA with 5′ overhangs, 3′ overhangs, and blunt ends in various combinations (Figure 2B). We will refer to eight structural categories of paired ends. Three categories are ligatable: compatible 3′–3′, 5′–5′, and blunt–blunt ends. Five categories require processing: noncompatible 3′–3′, 5′–5′, 3′–5′, blunt–3′, and blunt–5′ ends. Each of the last five categories includes paired ends attached to DNA1 and DNA2 in either orientation (Figure 1). For example, blunt–3′ ends include EcoRV–SacI, EcoRV–KpnI, and KpnI–EcoRV ends. Compatible 3′–3′ ends were usually joined most efficiently (12.3% for KpnI–KpnI, 9.0% for SacI–SacI), followed by compatible 5′–5′ ends (5.4% for BamHI–BamHI, 4.0% for EcoRI–EcoRI) and blunt–blunt ends (2.3% for StuI–EcoRV). These joining efficiencies were quite high, since they refer only to DNA ends joined in the orientation specified by the PCR primers. The total percentage of joined ends was significantly higher since the ends were joined in four possible orientations. Noncompatible ends were joined with varying efficiencies. Blunt–3′ ends (KpnI–EcoRV) were joined with 3.5% efficiency, while noncompatible 5′–5′ ends (BamHI–EcoRI) were joined with only 0.05% efficiency. This suggests that factors involved in processing 5′ ends were limiting in the extract. Compatible ends are joined without processing To characterize junctions formed by the NHEJ reaction, we subcloned PCR-amplified DNA sequences on both sides of the junctions and sequenced DNA from individual clones. We sequenced 10 junctions from each of three reactions involving compatible ends, KpnI–KpnI, BamHI–BamHI, and StuI–EcoRV. All 30 junctions were formed without processing (Figure 3A). The precise joining of compatible ends indicated that processing is suppressed when not required. Figure 3.Compatible ends are joined with minimal processing. DNA substrates containing compatible ends were incubated with (A) extract plus added dNTPs, or (B) extract in the absence of added dNTPs. The legends indicate joining efficiency to the left of the arrow, and total number of sequenced junctions to the right of the arrow. The number of times each junction was recovered is shown in the column labeled 'No'. When the DNA ends are processed, the open-mouthed icon and white background in the DNA indicate nuclease activity, and the arrow and black background indicate polymerase activity. Gray background indicates unprocessed DNA. Download figure Download PowerPoint Noncompatible ends are processed by DNA synthesis across a discontinuous template strand When reactions for noncompatible ends were performed with dNTPs added to the extract, the vast majority of junctions showed evidence of templated nucleotide addition (Figure 4). We sequenced 364 junctions and did not detect any mutations from templated addition of a total of 369 nucleotides. Thus, the error rate of the associated polymerase activity was less than 1%. Figure 4.In the presence of dNTPs, noncompatible ends are processed largely by templated nucleotide addition. DNA substrates with compatible or noncompatible ends were incubated with extract and dNTPs, and the junctions were sequenced. The processed ends are shown according to the legend in Figure 3. The number of bases of microhomology utilized in the joining reaction is shown in the column labeled 'MH'. Each section (A–E) depicts junctions from a different structural category of paired ends. Download figure Download PowerPoint The observed polymerase activity in our extract was not an artifact of the PCR assay. Omitting dNTPs from the reaction inhibited the joining efficiency of noncompatible ends (Figure 2) and suppressed the templated addition of nucleotides in the junctions (see below). Furthermore, adding the DNA polymerase inhibitor dideoxy-NTPs suppressed the joining efficiency of noncompatible ends, while preserving the joining efficiency of compatible ends (data not shown). Polymerase activity filled in 5′ overhanging ends, as expected. However, polymerase activity also filled in 3′ overhanging ends with high frequency (dotted arrows in Figure 4), a phenomenon previously observed in Xenopus extract (Thode et al, 1990). Indeed, blunt–3′ ends were joined with high efficiency (Figure 2B and Supplementary Figure 3B) and almost always processed by the fill-in of the 3′ end (Figure 4). Thus, a polymerase primed from the blunt end was able to synthesize DNA across a discontinuity in the template strand, perhaps in conjunction with a factor that aligned the ends appropriately. This type of polymerase activity may increase the efficiency of NHEJ by creating base pairing between the opposing ends and thus stabilizing their alignment. To further study the role of polymerase activity in the NHEJ reaction, we omitted dNTPs from the reaction. The joining efficiency of noncompatible ends was reduced 1.7-fold to over 200-fold, suggesting that polymerase activity made a large contribution to processing of the ends (Figure 2B and Supplementary Figure 3). By contrast, the joining efficiency of compatible ends did not change significantly (Figure 2B and Supplementary Figure 2). This is consistent with the absence of polymerase activity at the junctions of compatible ends (Figure 3). Noncompatible ends are processed by regulated nuclease activity To characterize the nuclease activity in NHEJ, we suppressed polymerase activity by omitting dNTPs. In these reactions, addition of wortmannin or immunodepletion of XRCC4 inhibited joining 80- to 5000-fold (data not shown). Thus, joining remained dependent on DNA-PKcs and XRCC4/Ligase4, and reflected bona fide NHEJ. Joining efficiency was significantly reduced in the absence of added dNTPs (Figure 2). When we sequenced the junctions formed from noncompatible ends, processing was dominated by nuclease activity, which was involved in the formation of 195 of 199 (98%) junctions (Figure 5). Modest polymerase activity was observed, presumably due to nucleotides generated by nuclease activity. For compatible ends, nuclease activity was suppressed, since those ends were almost always joined precisely (Figure 3B). Figure 5.When dNTPs are omitted, noncompatible ends are processed by deletion and templated addition of nucleotides. DNA substrates with noncompatible ends were incubated with extract in the absence of added dNTPs, and the processed ends are shown according to the legend in Figure 3. Asterisks indicate junctions that utilized microhomology from internal DNA sequences. In these cases, there was ambiguity in the processing events, and we assumed that the microhomology alignment occurred via a 3′ overhang. Each section (A–E) depicts junctions from a different structural category of paired ends. Download figure Download PowerPoint There were two types of nuclease activity. The first type was specific for single-stranded 5′ or 3′ overhangs. Many of the overhangs were removed precisely to leave a blunt end. This was particularly evident when the opposing end was already blunt. In 15 of 37 junctions from the blunt–3′ ends, EcoRV–KpnI and KpnI–EcoRV, the four terminal nucleotides were removed from the 3′ overhang (Figure 5B). Similarly, in 14 of 24 junctions from the blunt–5′ ends, StuI–BamHI, the four terminal nucleotides were removed from the 5′ overhang (Figure 5C). Figure 6.When dNTPs are omitted, noncompatible ends are processed by deletion and templated addition of nucleotides. DNA substrates with noncompatible ends were incubated with extract in the absence of added dNTPs, and the processed ends are shown according to the legend in Figure 3. Asterisks indicate junctions that utilized microhomology from internal DNA sequences. In these cases, there was ambiguity in the processing events, and we assumed that the microhomology alignment occurred via a 3′ overhang. Each section (A–E) depicts junctions from a different structural category of paired ends. Download figure Download PowerPoint The second type of nuclease activity produced deletions that were consistent with alignment of the DNA ends by base pairing in regions of microhomology. Deletions back to one to five bases of microhomology were observed in 148 of 199 (74%) junctions. The deletions were tightly regulated. Only eight junctions (4%) contained deletions larger than 16 nucleotides. Furthermore, all of the larger deletions were more than 150 nucleotides, consistent with the aberrant recruitment of an unregulated, processive nuclease. These large deletions became dominant in the rare junctions sequenced from reactions in which the kinase activity of DNA-PKcs was inhibited by wortmannin (data not shown). This suggests that when DNA-PKcs is kinase-dead, the junctions that were recovered involved backup nucleases that excised large DNA–protein fragments. When DNA-PKcs is active, its kinase activity may regulate the nuclease activity to control the size of deletions. Junctions utilized microhomology with sequences in 3′ overhangs much more frequently than with sequences in 5′ overhangs. Of the 66 total junctions from 3′–5′ ends, only one utilized microhomology pairing with nucleotides in a 5′ overhang, while 62 utilized a 3′ overhang. Among junctions from the noncompatible blunt–5′ ends, StuI–BamHI, only one of 24 utilized microhomology with the 5′ overhang (Figure 5C), while 15 of 37 junctions from the noncompatible blunt–3′ ends, EcoRV–KpnI and KpnI–EcoRV, utilized microhomology with the 3′ overhang (Figure 5B). Furthermore, 23 of 27 junctions from the noncompatible 3′–3′ ends, SacI–KpnI, utilized microhomology with a 3′ overhang (Figure 5D). The preference for utilizing 3′ overhangs during NHEJ could be coupled to key enzymatic activities. The DNA-PKcs kinase is activated more efficiently with 3′ overhangs than with 5′ overhangs (Hammarsten et al, 2000). The endonuclease that opens hairpin ends during V(D)J recombination preferentially creates ends with 3′ overhangs (Schlissel, 1998). Internal DNA sequence influences processing events during NHEJ We discovered up to 100-fold variations in the efficiency of joining noncompatible ends when different DNA molecules were used. To examine this variation in more detail, we constructed DNA molecules in which the noncompatible ends were exchanged relative to the internal sequences. We shall refer to the reactions for these exchanged noncompatible ends as 'matched reactions', as illustrated in Figure 1. Surprisingly, matched reactions often had different joining efficiencies. With dNTPs added to the reaction, EcoRV–BamHI was joined eight-fold more efficiently than BamHI–EcoRV (Supplementary Figure 3). With dNTPs omitted, some matched reactions showed even larger variations in joining efficiency. BamHI–SacI was joined 30-fold more efficiently than SacI–BamHI, and EcoRI–SacI was joined 40-fold more efficiently than SacI–EcoRI. Thus, sequences internal to the DNA ends influenced joining efficiency. To characterize the role of internal DNA sequence, we sequenced junctions from three pairs of matched reactions (Figure 5A, B and 5E). The matched reactions with noncompatible 5′ ends, BamHI–EcoRI and EcoRI–BamHI, were joined with the same low efficiency of 0.006%. Processing yielded a heterogeneous mixture of junctions, some showing templated addition of nucleotides, but most showing deletions back to regions of microhomology. For another pair of matched reactions, EcoRV–KpnI and KpnI–EcoRV (blunt–3′ ends), we found six-fold differences in joining efficiency of 0.093% and 0.015%, respectively. Part of the difference could arise from polymerase activity across a discontinuous template, which may enhance joining efficiency by creating base pairing to stabilize alignment of the ends. Indeed, polymerase activity was present in 3 of 17 KpnI–EcoRV junctions, but in 11 of 20 junctions from the more efficient EcoRV–KpnI reaction. The noncompatible 3′–5′ ends, SacI–EcoRI and SacI–BamHI, were joined 40- and 30-fold less efficiently than matched reactions in which the ends were exchanged, EcoRI–SacI and BamHI–SacI (Figure 5E). In the more efficient reactions, all 18 EcoRI–SacI junctions and 14 of 16 BamHI–SacI junctions utilized polymerase activity. Thus, higher joining efficiency was associated with increased polymerase activity, which often created base pairing by synthesis across a discontinuous template. The more efficient reactions also involved microhomology pairing of the terminal two bases of the SacI 3′ overhang with two internal bases near the opposing end, and included nuclease activity directed at only one of the four DNA strands. In the less efficient SacI–EcoRI and SacI–BamHI reactions, microhomology pairing with the terminal two bases of the SacI 3′ overhang was not available for at least 20 bp. Instead, microhomology base pairing was achieved by recruitment of nuclease activity to at least two of the four DNA strands. Thus, the recruitment of nuclease activity appeared to be inefficient, biasing the NHEJ in favor of preserving DNA sequence. These data demonstrate that internal DNA sequence influences the spectrum of processing events for noncompatible ends. Internal DNA sequence influences joining efficiency in the absence of processing To further examine the role of internal DNA sequence, we used DNA substrates with five types of blunt DNA ends in 11 separate reactions (Figure 6). As expected, T4 ligase joined all blunt ends with similar efficiency. By contrast, extract joined blunt ends with efficiencies that varied up to 21-fold. For example, SspI–SwaI (2.10%) was joined 19-fold more efficiently than its matched pair of ends, SwaI–SspI (0.11%). Addition of dNTPs did not significantly affect the joining efficiencies of any of these blunt ends (Supplementary Figure 2). Thus, internal DNA sequence strongly influenced the joining efficiency for blunt ends. Figure 7.Joining efficiency of blunt DNA ends is influenced by internal DNA sequence. Joining efficiency was measured after incubating DNA substrates with T4 DNA ligase, or after incubating the same DNA substrates with extract. In these experiments, the reactions were performed in the absence of added dNTPs. Download figure Download PowerPoint We sequenced DNA junctions from four different blunt–blunt reactions that showed large variations in joining efficiency (Supplementary Figure 4). The ends were joined without processing in 49 of 53 sequenced junctions, despite a 19-fold variation in joining efficiency. Thus, we were confronted with the striking result that internal DNA sequence influenced the efficiency of blunt end-joining, even though 95% of the joining occurred without processing. We considered two possible explanations for how DNA sequence might affect the joining efficiency of blunt ends. First, DNA sequence that permitted microhomology base pairing or the formation of cruciform structures might influence the joining reaction. Second, DNA sequence might affect the interaction of the DNA with DNA-PKcs. To address the first possibility, we constructed blunt-ended DNA fragments containing up to six bases of microhomology internal to both ends, or containing inverted repeats of up to six bases that would permit formation of a cruciform structure at the ends. Although we observed large variations in the joining efficiency of these blunt ends, there was no correlation with the presence of microhomology or inverted repeats in the paired ends (data not shown). Thus, we were led to the hypothesis that DNA sequence affects the interaction of the ends with DNA-PKcs. How this interaction might depend on DNA sequence will be explored in Discussion. Furthermore, our hypothesis is supported by recent data that sequence strongly influences kinase activation (Pawelczak et al, 2005). Discussion NHEJ in extract has the properties of NHEJ in vivo It is difficult to study NHEJ in vivo since junctions can be recovered only if the double-strand breaks occur at a defined site. Rouet et al (1994) introduced I–SceI sites into mouse chromosomal DNA and created double-strand breaks by expressing the restriction enzyme I–SceI. The junctions contained various deletions back to short regions of microhomology. A follow-up experiment introduced I–SceI sites into wild-type and Ku-deficient CHO cells (Liang et al, 1996). The site was engineered so that repair of the double-strand break would reconstruct a wild-type neomycin resistance gene if joining occurred after deletion back to a region containing four base pairs of microhomology. Ku-deficient cells were appropriately deficient in rejoining ends by this deletion mechanism. However, characterization of NHEJ in vivo was limited because the double-strand breaks involved only a single sequence with a 3′ overhang. Furthermore, junctions in the Ku-dependent reaction were selected for a single processing event. NHEJ in vivo has been studied indirectly in the context of V(D)J recombination. The RAG1/RAG2 complex cleaves the chromosome at two recombination signal sequences to create two hairpin-coding ends and two blunt signal ends. The joining of signal ends occurs without processing and requires Ku and XRCC4/Ligase4. The hairpin-coding ends are opened preferentially into 3′ overhangs in vivo by an endonuclease activity (Schlissel, 1998), most likely Artemis (Ma et al, 2002). The opened coding ends are processed and joined in a reaction requiring Ku, DNA-PKcs, and XRCC4/Ligase4. P
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