DNA Ligase III Promotes Alternative Nonhomologous End-Joining during Chromosomal Translocation Formation
Nonhomologous end-joining (NHEJ) is the primary DNA repair pathway thought to underlie chromosomal translocations and other genomic rearrangements in somatic cells. The canonical NHEJ pathway, including DNA ligase IV (Lig4), suppresses genomic instability and chromosomal translocations, leading to the notion that a poorly defined, alternative NHEJ (alt-NHEJ) pathway generates these rearrangements. Here, we investigate the DNA ligase requirement of chromosomal translocation formation in mouse cells. Mammals have two other DNA ligases, Lig1 and Lig3, in addition to Lig4. As deletion of Lig3 results in cellular lethality due to its requirement in mitochondria, we used recently developed cell lines deficient in nuclear Lig3 but rescued for mitochondrial DNA ligase activity. Further, zinc finger endonucleases were used to generate DNA breaks at endogenous loci to induce translocations. Unlike with Lig4 deficiency, which causes an increase in translocation frequency, translocations are reduced in frequency in the absence of Lig3. Residual translocations in Lig3-deficient cells do not show a bias toward use of pre-existing microhomology at the breakpoint junctions, unlike either wild-type or Lig4-deficient cells, consistent with the notion that alt-NHEJ is impaired with Lig3 loss. By contrast, Lig1 depletion in otherwise wild-type cells does not reduce translocations or affect microhomology use. However, translocations are further reduced in Lig3-deficient cells upon Lig1 knockdown, suggesting the existence of two alt-NHEJ pathways, one that is biased toward microhomology use and requires Lig3 and a back-up pathway which does not depend on microhomology and utilizes Lig1.
Vyšlo v časopise:
DNA Ligase III Promotes Alternative Nonhomologous End-Joining during Chromosomal Translocation Formation. PLoS Genet 7(6): e32767. doi:10.1371/journal.pgen.1002080
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1002080
Souhrn
Nonhomologous end-joining (NHEJ) is the primary DNA repair pathway thought to underlie chromosomal translocations and other genomic rearrangements in somatic cells. The canonical NHEJ pathway, including DNA ligase IV (Lig4), suppresses genomic instability and chromosomal translocations, leading to the notion that a poorly defined, alternative NHEJ (alt-NHEJ) pathway generates these rearrangements. Here, we investigate the DNA ligase requirement of chromosomal translocation formation in mouse cells. Mammals have two other DNA ligases, Lig1 and Lig3, in addition to Lig4. As deletion of Lig3 results in cellular lethality due to its requirement in mitochondria, we used recently developed cell lines deficient in nuclear Lig3 but rescued for mitochondrial DNA ligase activity. Further, zinc finger endonucleases were used to generate DNA breaks at endogenous loci to induce translocations. Unlike with Lig4 deficiency, which causes an increase in translocation frequency, translocations are reduced in frequency in the absence of Lig3. Residual translocations in Lig3-deficient cells do not show a bias toward use of pre-existing microhomology at the breakpoint junctions, unlike either wild-type or Lig4-deficient cells, consistent with the notion that alt-NHEJ is impaired with Lig3 loss. By contrast, Lig1 depletion in otherwise wild-type cells does not reduce translocations or affect microhomology use. However, translocations are further reduced in Lig3-deficient cells upon Lig1 knockdown, suggesting the existence of two alt-NHEJ pathways, one that is biased toward microhomology use and requires Lig3 and a back-up pathway which does not depend on microhomology and utilizes Lig1.
Zdroje
1. ManiRSChinnaiyanAM 2010 Triggers for genomic rearrangements: insights into genomic, cellular and environmental influences. Nat Rev Genet 11 819 829
2. WeinstockDMElliottBJasinM 2006 A model of oncogenic rearrangements: differences between chromosomal translocation mechanisms and simple double-strand break repair. Blood 107 777 780
3. LieberMR 2010 The Mechanism of Double-Strand DNA Break Repair by the Nonhomologous DNA End-Joining Pathway. Annu Rev Biochem
4. JeggoPA 1998 Identification of genes involved in repair of DNA double-strand breaks in mammalian cells. Radiat Res 150 S80 91
5. LieberMRMaYPannickeUSchwarzK 2003 Mechanism and regulation of human non-homologous DNA end-joining. Nat Rev Mol Cell Biol 4 712 720
6. DifilippantonioMJPetersenSChenHTJohnsonRJasinM 2002 Evidence for replicative repair of DNA double-strand breaks leading to oncogenic translocation and gene amplification. J Exp Med 196 469 480
7. ZhuCMillsKDFergusonDOLeeCManisJ 2002 Unrepaired DNA breaks in p53-deficient cells lead to oncogenic gene amplification subsequent to translocations. Cell 109 811 821
8. WeinstockDMBrunetEJasinM 2007 Formation of NHEJ-derived reciprocal chromosomal translocations does not require Ku70. Nat Cell Biol 9 978 981
9. SimsekDJasinM 2010 Alternative end-joining is suppressed by the canonical NHEJ component Xrcc4-ligase IV during chromosomal translocation formation. Nat Struct Mol Biol 17 410 416
10. LiangFJasinM 1996 Ku80-deficient cells exhibit excess degradation of extrachromosomal DNA. J Biol Chem 271 14405 14411
11. DelacoteFHanMStamatoTDJasinMLopezBS 2002 An xrcc4 defect or Wortmannin stimulates homologous recombination specifically induced by double-strand breaks in mammalian cells. Nucleic Acids Res 30 3454 3463
12. Guirouilh-BarbatJHuckSBertrandPPirzioLDesmazeC 2004 Impact of the KU80 pathway on NHEJ-induced genome rearrangements in mammalian cells. Mol Cell 14 611 623
13. Guirouilh-BarbatJRassEPloIBertrandPLopezBS 2007 Defects in XRCC4 and KU80 differentially affect the joining of distal nonhomologous ends. Proc Natl Acad Sci U S A 104 20902 20907
14. YanCTBoboilaCSouzaEKFrancoSHickernellTR 2007 IgH class switching and translocations use a robust non-classical end-joining pathway. Nature 449 478 482
15. CorneoBWendlandRLDerianoLCuiXKleinIA 2007 Rag mutations reveal robust alternative end joining. Nature 449 483 486
16. FattahFLeeEHWeisenselNWangYLichterN 2010 Ku regulates the non-homologous end joining pathway choice of DNA double-strand break repair in human somatic cells. PLoS Genet 6 e1000855
17. RassEGrabarzAPloIGautierJBertrandP 2009 Role of Mre11 in chromosomal nonhomologous end joining in mammalian cells. Nat Struct Mol Biol 16 819 824
18. DinkelmannMSpehalskiEStonehamTBuisJWuY 2009 Multiple functions of MRN in end-joining pathways during isotype class switching. Nat Struct Mol Biol 16 808 813
19. XieAKwokAScullyR 2009 Role of mammalian Mre11 in classical and alternative nonhomologous end joining. Nat Struct Mol Biol 16 814 818
20. BennardoNChengAHuangNStarkJM 2008 Alternative-NHEJ is a mechanistically distinct pathway of mammalian chromosome break repair. PLoS Genet 4 e1000110
21. ZhangYJasinM 2011 An essential role for CtIP in chromosomal translocation formation through an alternative end-joining pathway. Nat Struct Mol Biol 18 80 84
22. Lee-TheilenMMatthewsAJKellyDZhengSChaudhuriJ 2011 CtIP promotes microhomology-mediated alternative end joining during class-switch recombination. Nat Struct Mol Biol 18 75 79
23. AudebertMSallesBCalsouP 2004 Involvement of poly(ADP-ribose) polymerase-1 and XRCC1/DNA ligase III in an alternative route for DNA double-strand breaks rejoining. J Biol Chem 279 55117 55126
24. WangMWuWRosidiBZhangLWangH 2006 PARP-1 and Ku compete for repair of DNA double strand breaks by distinct NHEJ pathways. Nucleic Acids Res 34 6170 6182
25. EllenbergerTTomkinsonAE 2008 Eukaryotic DNA ligases: structural and functional insights. Annu Rev Biochem 77 313 338
26. SimsekDFurdaAGaoYArtusJBrunetE 2011 Crucial role for DNA ligase III in mitochondria but not in Xrcc1-dependent repair. Nature 471 245 248
27. GaoYKatyalSLeeYZhaoJRehgJE 2011 DNA ligase III is critical for mtDNA integrity but not Xrcc1-mediated nuclear DNA repair. Nature 471 240 244
28. CaldecottKWMcKeownCKTuckerJDLjungquistSThompsonLH 1994 An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III. Mol Cell Biol 14 68 76
29. NashRACaldecottKWBarnesDELindahlT 1997 XRCC1 protein interacts with one of two distinct forms of DNA ligase III. Biochemistry 36 5207 5211
30. WangHRosidiBPerraultRWangMZhangL 2005 DNA ligase III as a candidate component of backup pathways of nonhomologous end joining. Cancer Res 65 4020 4030
31. Puebla-OsorioNLaceyDBAltFWZhuC 2006 Early embryonic lethality due to targeted inactivation of DNA ligase III. Mol Cell Biol 26 3935 3941
32. MortusewiczORothbauerUCardosoMCLeonhardtH 2006 Differential recruitment of DNA Ligase I and III to DNA repair sites. Nucleic Acids Res 34 3523 3532
33. HendersonBREleftheriouA 2000 A comparison of the activity, sequence specificity, and CRM1-dependence of different nuclear export signals. Exp Cell Res 256 213 224
34. UrnovFDRebarEJHolmesMCZhangHSGregoryPD 2010 Genome editing with engineered zinc finger nucleases. Nat Rev Genet 11 636 646
35. BrunetESimsekDTomishimaMDeKelverRChoiVM 2009 Chromosomal translocations induced at specified loci in human stem cells. Proc Natl Acad Sci U S A 106 10620 10625
36. LeppardJBDongZMackeyZBTomkinsonAE 2003 Physical and functional interaction between DNA ligase IIIalpha and poly(ADP-Ribose) polymerase 1 in DNA single-strand break repair. Mol Cell Biol 23 5919 5927
37. TaylorRMWhitehouseCJCaldecottKW 2000 The DNA ligase III zinc finger stimulates binding to DNA secondary structure and promotes end joining. Nucleic Acids Res 28 3558 3563
38. Cotner-GoharaEKimIKTomkinsonAEEllenbergerT 2008 Two DNA-binding and nick recognition modules in human DNA ligase III. J Biol Chem 283 10764 10772
39. StephensPJMcBrideDJLinMLVarelaIPleasanceED 2009 Complex landscapes of somatic rearrangement in human breast cancer genomes. Nature 462 1005 1010
40. BoboilaCJankovicMYanCTWangJHWesemannDR 2010 Alternative end-joining catalyzes robust IgH locus deletions and translocations in the combined absence of ligase 4 and Ku70. Proc Natl Acad Sci U S A 107 3034 3039
41. LieberMRWilsonTE SnapShot: Nonhomologous DNA end joining (NHEJ). Cell 142 496 496 e491
42. HockemeyerDSoldnerFBeardCGaoQMitalipovaM 2009 Efficient targeting of expressed and silent genes in human ESCs and iPSCs using zinc-finger nucleases. Nat Biotechnol 27 851 857
43. UrnovFDMillerJCLeeYLBeausejourCMRockJM 2005 Highly efficient endogenous human gene correction using designed zinc-finger nucleases. Nature 435 646 651
44. GoldbergADBanaszynskiLANohKMLewisPWElsaesserSJ 2010 Distinct factors control histone variant H3.3 localization at specific genomic regions. Cell 140 678 691
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Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
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