RESUMO
DNA interstrand crosslinks (ICL) present a major threat to cell viability and genome integrity. In eukaryotic cells, the ICLs have been suggested to be repaired by a complex process involving Xpf/Ercc1-mediated endonucleolytic incision and homologous recombination (HR). However, the entire feature of the ICL tolerating mechanism is still poorly understood. Here we studied chromosome aberrations (CA) and sister chromatid exchanges (SCE) by the use of the crosslinking agent mitomycin C (MMC), in chicken DT40 cells with the HR genes disrupted by targeted replacement. The disruption of the Rad54, Rad51B, Rad51C, Rad51D, Xrcc2 and Xrcc3 genes resulted in a dramatic reduction of spontaneous and MMC-induced SCEs. Interestingly, while HR-deficient cells were hypersensitive to cell killing by MMC, MMC-induced CAs were also suppressed in the HR-deficient cells except for Rad51D-, Xrcc2- and Xrcc3-deficient cells. These observations indicate that DNA double strand breaks (DSB) at stalled replication forks and those arising as repair intermediates present strong signals to cell death but can be tolerated by the HR repair pathway, where Rad54, Rad51B and Rad51C have an initiative role and repair can be completed by their paralogs Rad51D, Xrcc2 and Xrcc3. The impairment of the HR pathway, which otherwise leads to cell death, may be somewhat substituted by an alternative mechanism such as the Mre11/Rad50/Nbs1 pathway, resulting in reduced frequencies of SCEs and CAs.
Assuntos
Linfócitos B/metabolismo , Aberrações Cromossômicas , Reagentes de Ligações Cruzadas/farmacologia , Enzimas Reparadoras do DNA/fisiologia , Reparo do DNA/fisiologia , DNA/genética , Mitomicina/farmacologia , Recombinação Genética , Animais , Linfócitos B/efeitos dos fármacos , Linfócitos B/ultraestrutura , Morte Celular , Células Cultivadas/efeitos dos fármacos , Células Cultivadas/metabolismo , Células Cultivadas/ultraestrutura , Galinhas , DNA/efeitos dos fármacos , Dano ao DNA , Enzimas Reparadoras do DNA/genética , Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/fisiologia , Marcação de Genes , Modelos Genéticos , Troca de Cromátide Irmã/efeitos dos fármacosRESUMO
For successful eukaryotic mitosis, sister chromatid pairs remain linked after replication until their kinetochores have been attached to opposite spindle poles by microtubules. This linkage is broken at the metaphase-anaphase transition and the sisters separate. In budding yeast, this sister chromatid cohesion requires a multi-protein complex called cohesin. A key component of cohesin is Scc1/Mcd1 (Rad21 in fission yeast). Disruption of the chicken orthologue of Scc1 by gene targeting in DT40 cells causes premature sister chromatid separation. Cohesion between sister chromatids is likely to provide a substrate for post-replicative DNA repair by homologous recombination. In keeping with this role of cohesion, Scc1 mutants also show defects in the repair of spontaneous and induced DNA damage. Scc1-deficient cells frequently fail to complete metaphase chromosome alignment and show chromosome segregation defects, suggesting aberrant kinetochore function. Consistent with this, the chromosomal passenger protein, INCENP (inner centromere protein) fails to localize to centromeres. Survivin, another passenger protein and one which interacts with INCENP, also fails to localize to centromeres in Scc1-deficient cells. These results show that cohesin maintains genomic stability by ensuring appropriate DNA repair and equal chromosome segregation at mitosis.
Assuntos
Cromátides/ultraestrutura , Reparo do DNA , Recombinação Genética , Animais , Proteínas de Ciclo Celular , Linhagem Celular , Galinhas , Proteínas Cromossômicas não Histona , Proteínas Fúngicas , Genoma , Proteínas Inibidoras de Apoptose , Proteínas Associadas aos Microtúbulos/metabolismo , Mitose , Proteínas de Neoplasias , Proteínas Nucleares/metabolismo , Proteínas Nucleares/fisiologia , Fuso Acromático , Survivina , CoesinasRESUMO
Proteolytic cleavage of the cohesin subunit Scc1 is a consistent feature of anaphase onset, although temporal differences exist between eukaryotes in cohesin loss from chromosome arms, as distinct from centromeres. We describe the effects of genetic deletion of Scc1 in chicken DT40 cells. Scc1 loss caused premature sister chromatid separation but did not disrupt chromosome condensation. Scc1 mutants showed defective repair of spontaneous and induced DNA damage. Scc1-deficient cells frequently failed to complete metaphase chromosome alignment and showed chromosome segregation defects, suggesting aberrant kinetochore function. Notably, the chromosome passenger INCENP did not localize normally to centromeres, while the constitutive kinetochore proteins CENP-C and CENP-H behaved normally. These results suggest a role for Scc1 in mitotic regulation, along with cohesion.
Assuntos
Proteínas de Ciclo Celular/metabolismo , Ciclo Celular/fisiologia , Cromátides/metabolismo , Cinetocoros/metabolismo , Animais , Antibacterianos/farmacologia , Proteínas de Ciclo Celular/genética , Linhagem Celular , Núcleo Celular/metabolismo , Galinhas , Proteínas Cromossômicas não Histona/genética , Proteínas Cromossômicas não Histona/metabolismo , Reparo do DNA , Doxiciclina/farmacologia , Citometria de Fluxo , Proteínas Fúngicas , Humanos , Hibridização in Situ Fluorescente , Substâncias Macromoleculares , Microscopia de Força Atômica , Microscopia de Fluorescência , Proteínas Nucleares/metabolismo , Fenótipo , Fosfoproteínas , Subunidades Proteicas , Proteínas Recombinantes de Fusão/genética , Proteínas Recombinantes de Fusão/metabolismo , Proteínas de Saccharomyces cerevisiae , CoesinasRESUMO
Two major complementary double-strand break (DSB) repair pathways exist in vertebrates, homologous recombination (HR), which involves Rad54, and non-homologous end-joining, which requires the DNA-dependent protein kinase (DNA-PK). DNA-PK comprises a catalytic subunit (DNA-PKcs) and a DNA-binding Ku70 and Ku80 heterodimer. To define the activities of individual DNA-PK components in DSB repair, we targeted the DNA-PKcs gene in chicken DT40 cells. DNA-PKcs deficiency caused a DSB repair defect that was, unexpectedly, suppressed by KU70 disruption. We have shown previously that genetic ablation of Ku70 confers RAD54-dependent radioresistance on S-G(2) phase cells, when sister chromatids are available for HR repair. To test whether direct interference by Ku70 with HR might explain the Ku70(-/-)/DNA-PKcs(-/-/-) radioresistance, we monitored HR activities directly in Ku- and DNA-PKcs-deficient cells. The frequency of intrachromosomal HR induced by the I-SceI restriction enzyme was increased in the absence of Ku but not of DNA-PKcs. Significantly, abrogation of HR activity by targeting RAD54 in Ku70(-/-) or DNA-PKcs(-/-/-) cells caused extreme radiosensitivity, suggesting that the relative radioresistance seen with loss of Ku70 was because of HR-dependent repair pathways. Our findings suggest that Ku can interfere with HR-mediated DSB repair, perhaps competing with HR for DSB recognition.
Assuntos
Antígenos Nucleares , Dano ao DNA , DNA Helicases , Reparo do DNA , Proteínas de Ligação a DNA/fisiologia , DNA/metabolismo , Proteínas Nucleares/fisiologia , Proteínas Serina-Treonina Quinases/genética , Animais , Western Blotting , Ciclo Celular , Linhagem Celular , Galinhas , Cromátides/fisiologia , Proteína Quinase Ativada por DNA , Dimerização , Relação Dose-Resposta à Radiação , Éxons , Fase G2 , Genótipo , Autoantígeno Ku , Camundongos , Nocodazol/farmacologia , Proteínas Serina-Treonina Quinases/metabolismo , Recombinação Genética , Fase SRESUMO
Yeast Rad52 DNA-repair mutants exhibit pronounced radiation sensitivity and a defect in homologous re combination (HR), whereas vertebrate cells lacking Rad52 exhibit a nearly normal phenotype. Bio chemical studies show that both yeast Rad52 and Rad55-57 (Rad51 paralogs) stimulate DNA-strand exchange mediated by Rad51. These findings raise the possibility that Rad51 paralogs may compensate for lack of Rad52 in vertebrate cells, explaining the absence of prominent phenotypes for Rad52-deficient cells. To test this hypothesis, using chicken DT40 cells, we generated conditional mutants deficient in both RAD52 and XRCC3, which is one of the five vertebrate RAD51 paralogs. Surprisingly, the rad52 xrcc3 double-mutant cells were non-viable and exhibited extensive chromosomal breaks, whereas rad52 and xrcc3 single mutants grew well. Our data reveal an overlapping (but non-reciprocal) role for Rad52 and XRCC3 in repairing DNA double-strand breaks. The present study shows that Rad52 can play an important role in HR repair by partially substituting for a Rad51 paralog.
Assuntos
Cromossomos/genética , Reparo do DNA , Proteínas de Ligação a DNA/metabolismo , Animais , Proteínas Aviárias , Evolução Biológica , Proteínas de Ligação a DNA/genética , Genes Letais , Humanos , Rad51 Recombinase , Recombinação GenéticaAssuntos
Divisão Celular/genética , Reparo do DNA , Recombinação Genética , Animais , Galinhas , DNA , Reparo do DNA/genética , Reparo do DNA/fisiologia , Replicação do DNA , Genoma , HumanosRESUMO
The RAD52 epistasis group genes are involved in homologous DNA recombination, and their primary structures are conserved from yeast to humans. Although biochemical studies have suggested that the fundamental mechanism of homologous DNA recombination is conserved from yeast to mammals, recent studies of vertebrate cells deficient in genes of the RAD52 epistasis group reveal that the role of each protein is not necessarily the same as that of the corresponding yeast gene product. This review addresses the roles and mechanisms of homologous recombination-mediated repair with a special emphasis on differences between yeast and vertebrate cells.
Assuntos
Reparo do DNA , Proteínas de Ligação a DNA/fisiologia , Recombinação Genética , Alelos , Animais , Sobrevivência Celular , Galinhas , Dano ao DNA , Proteínas Fúngicas/fisiologia , Humanos , Proteína Rad52 de Recombinação e Reparo de DNA , Saccharomyces cerevisiae/genética , Proteínas de Saccharomyces cerevisiae , Vertebrados/genéticaRESUMO
Rejoining of ionizing radiation (IR) induced DNA DSBs usually follows biphasic kinetics with a fast (t(50): 5-30 min) component attributed to DNA-PK-dependent non-homologous endjoining (NHEJ) and a slow (t(50): 1-20 h), as of yet uncharacterized, component. To examine whether homologous recombination (HR) contributes to DNA DSB rejoining, a systematic genetic study was undertaken using the hyper-recombinogenic DT40 chicken cell line and a series of mutants defective in HR. We show that DT40 cells rejoin IR-induced DNA DSBs with half times of 13 min and 4.5 h and contributions by the fast (78%) and the slow (22%) components similar to those of other vertebrate cells with 1000-fold lower levels of HR. We also show that deletion of RAD51B, RAD52 and RAD54 leaves unchanged the rejoining half times and the contribution of the slow component, as does also a conditional knock out mutant of RAD51. A significant reduction (to 37%) in the contribution of the fast component is observed in Ku70(-/-) DT40 cells, but the slow component, operating with a half time of 18.4 h, is still able to rejoin the majority (63%) of DSBs. A double mutant Ku70(-/-)/RAD54(-/-) shows similar half times to Ku70(-/-) cells. Thus, variations in HR by several orders of magnitude leave unchanged the kinetics of rejoining of DNA DSBs, and fail to modify the contribution of the slow component in a way compatible with a dependence on HR. We propose that, in contrast to yeast, cells of vertebrates are 'hard-wired' in the utilization of NHEJ as the main pathway for rejoining of IR-induced DNA DSBs and speculate that the contribution of homologous recombination repair (HRR) is at a stage after the initial rejoining.
Assuntos
Reparo do DNA/fisiologia , Proteínas de Ligação a DNA/genética , Epistasia Genética , Recombinação Genética/fisiologia , Animais , Linhagem Celular , Galinhas , DNA/genética , DNA/metabolismo , DNA/efeitos da radiação , Dano ao DNA , Reparo do DNA/genética , CinéticaRESUMO
The Rad51 protein, a eukaryotic homologue of Escherichia coli RecA, plays a central role in both mitotic and meiotic homologous DNA recombination (HR) in Saccharomyces cerevisiae and is essential for the proliferation of vertebrate cells. Five vertebrate genes, RAD51B, -C, and -D and XRCC2 and -3, are implicated in HR on the basis of their sequence similarity to Rad51 (Rad51 paralogs). We generated mutants deficient in each of these proteins in the chicken B-lymphocyte DT40 cell line and report here the comparison of four new mutants and their complemented derivatives with our previously reported rad51b mutant. The Rad51 paralog mutations all impair HR, as measured by targeted integration and sister chromatid exchange. Remarkably, the mutant cell lines all exhibit very similar phenotypes: spontaneous chromosomal aberrations, high sensitivity to killing by cross-linking agents (mitomycin C and cisplatin), mild sensitivity to gamma rays, and significantly attenuated Rad51 focus formation during recombinational repair after exposure to gamma rays. Moreover, all mutants show partial correction of resistance to DNA damage by overexpression of human Rad51. We conclude that the Rad51 paralogs participate in repair as a functional unit that facilitates the action of Rad51 in HR.
Assuntos
Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/metabolismo , Animais , Proteínas Aviárias , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Sobrevivência Celular/efeitos da radiação , Galinhas , Cromossomos/genética , Reagentes de Ligações Cruzadas/farmacologia , Reparo do DNA , Raios gama , Deleção de Genes , Marcação de Genes , Teste de Complementação Genética , Humanos , Fenótipo , Rad51 Recombinase , Recombinação GenéticaRESUMO
DT40 is an avian leucosis virus-transformed chicken B-lymphocyte line which exhibits high ratios of targeted to random integration of transfected DNA constructs. This efficient targeted integration may be related to the ongoing diversification of the variable segment of the immunoglobulin gene through homologous DNA recombination-controlled gene conversion. DT40s are a convenient model system for making gene-targeted mutants. Another advantage is the relative tractability of these cells, which makes it possible to disrupt multiple genes in a single cell and to generate conditionally gene-targeted mutants including temperature-sensitive mutants. There are strong phenotypic similarities between murine and DT40 mutants of various genes involved in DNA recombination. These similarities confirm that the DT40 cell line is a reasonable model for the analysis of vertebrate DNA recombination, despite obvious concerns associated with the use of a transformed cell line, which may have certain cell-line-specific characteristics. Here we describe our studies of homologous DNA recombination in vertebrate somatic cells using reverse genetics in DT40 cells.
Assuntos
Linfócitos B/citologia , Dano ao DNA/genética , Reparo do DNA/genética , Mutação , Recombinação Genética , Animais , Linfócitos B/fisiologia , Linfócitos B/virologia , Ciclo Celular/genética , Linhagem Celular , Sobrevivência Celular/genética , Galinhas , Replicação do DNA , Técnicas GenéticasRESUMO
DT40 is a chicken B lymphocyte cell line that exhibits a high ratio of targeted and random integration of transfected DNA constructs. Using the DT40 cell line makes it comparatively easy to disrupt multiple genes in a single cell and to generate conditional targeted mutants including tet-controlled cre-lox-mediated and temperature-sensitive mutants. The DT40 mutants show a strong phenotypic resemblance to murine mutants with respect to genes involved in DNA recombination and repair. Because of these characteristics, DT40 is an attractive model for the analysis of DNA recombination and repair studies in vertebrates despite obvious concerns associated with the use of a transformed cell line that may have certain cell-line-specific characteristics. We present experimental evidence to demonstrate the usefulness of the DT40 cell line as a unique model to study DNA damaging events and their associated repair pathways.
Assuntos
Dano ao DNA , Reparo do DNA , Linfócitos/fisiologia , Recombinação Genética , Animais , Linhagem Celular , Galinhas , Modelos Animais de Doenças , Camundongos , TransfecçãoRESUMO
The highly conserved Saccharomyces cerevisiae Rad51 protein plays a central role in both mitotic and meiotic homologous DNA recombination. Seven members of the Rad51 family have been identified in vertebrate cells, including Rad51, Dmc1, and five Rad51-related proteins referred to as Rad51 paralogs, which share 20 to 30% sequence identity with Rad51. In chicken B lymphocyte DT40 cells, we generated a mutant with RAD51B/RAD51L1, a member of the Rad51 family, knocked out. RAD51B(-/-) cells are viable, although spontaneous chromosomal aberrations kill about 20% of the cells in each cell cycle. Rad51B deficiency impairs homologous recombinational repair (HRR), as measured by targeted integration, sister chromatid exchange, and intragenic recombination at the immunoglobulin locus. RAD51B(-/-) cells are quite sensitive to the cross-linking agents cisplatin and mitomycin C and mildly sensitive to gamma-rays. The formation of damage-induced Rad51 nuclear foci is much reduced in RAD51B(-/-) cells, suggesting that Rad51B promotes the assembly of Rad51 nucleoprotein filaments during HRR. These findings show that Rad51B is important for repairing various types of DNA lesions and maintaining chromosome integrity.
Assuntos
Reparo do DNA , Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/fisiologia , Recombinação Genética , Proteínas de Saccharomyces cerevisiae , Sequência de Aminoácidos , Animais , Northern Blotting , Western Blotting , Divisão Celular/efeitos dos fármacos , Divisão Celular/genética , Linhagem Celular , Separação Celular , Galinhas , Aberrações Cromossômicas , Cisplatino/farmacologia , DNA Helicases , Reparo do DNA/efeitos dos fármacos , Reparo do DNA/genética , Enzimas Reparadoras do DNA , DNA Complementar/metabolismo , Citometria de Fluxo , Proteínas Fúngicas/genética , Proteínas Fúngicas/fisiologia , Raios gama , Biblioteca Gênica , Marcação de Genes , Mitomicina/farmacologia , Modelos Genéticos , Dados de Sequência Molecular , Mutagênese , Inibidores da Síntese de Ácido Nucleico/farmacologia , Fenótipo , Radiossensibilizantes/farmacologia , Recombinação Genética/efeitos dos fármacos , Recombinação Genética/genética , Homologia de Sequência de Aminoácidos , Troca de Cromátide IrmãRESUMO
Bloom's syndrome (BS) is a rare genetic disorder and the cells from BS patients show genomic instability and an increased level of sister chromatid exchange (SCE). We generated BLM(-/-) and BLM(-/-)/RAD54(-/-) DT40 cells from the chicken B-lymphocyte line DT40. The BLM(-/-) DT40 cells showed higher sensitivity to methyl methanesulfonate and elevated levels of SCE as expected. The targeted integration frequency was also increased remarkably in BLM(-/-) cells. The SCE frequency increase in BLM(-/-) cells was considerably reduced and the enhanced targeted integration observed in BLM(-/-) cells was almost completely abolished in BLM(-/-)/RAD54(-/-) cells, indicating that a large portion of the SCE in BLM(-/-) cells occurs via homologous recombination, and homologous recombination events increase with the defect of BLM function. The BLM(-/-)/RAD54(-/-) cells showed a slow growth phenotype and an increased incidence of chromosome-type breaks/gaps while each single mutant showed relatively small numbers of chromosome-type breaks/gaps.
Assuntos
Adenosina Trifosfatases/metabolismo , Dano ao DNA , DNA Helicases/metabolismo , Replicação do DNA , Proteínas de Saccharomyces cerevisiae , Adenosina Trifosfatases/química , Adenosina Trifosfatases/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Síndrome de Bloom/metabolismo , Camptotecina/farmacologia , Ciclo Celular , Células Cultivadas , Galinhas , Aberrações Cromossômicas , DNA Helicases/química , DNA Helicases/genética , Primers do DNA , Enzimas Reparadoras do DNA , Etoposídeo/farmacologia , Proteínas Fúngicas/genética , Metanossulfonato de Metila/farmacologia , Dados de Sequência Molecular , RecQ Helicases , Homologia de Sequência de AminoácidosRESUMO
The human genetic disorder ataxia telangiectasia (A-T), caused by mutation in the ATM gene, is characterized by chromosomal instability, radiosensitivity and defective cell cycle checkpoint activation. DNA double-strand breaks (dsbs) persist in A-T cells after irradiation, but the underlying defect is unclear. To investigate ATM's interactions with dsb repair pathways, we disrupted ATM along with other genes involved in the principal, complementary dsb repair pathways of homologous recombination (HR) or non-homologous end-joining (NHEJ) in chicken DT40 cells. ATM(-/-) cells show altered kinetics of radiation-induced Rad51 and Rad54 focus formation. Ku70-deficient (NHEJ(-)) ATM(-/-) chicken DT40 cells show radiosensitivity and high radiation-induced chromosomal aberration frequencies, while Rad54-defective (HR(-)) ATM(-/-) cells show only slightly elevated aberration levels after irradiation, placing ATM and HR on the same pathway. These results reveal that ATM defects impair HR-mediated dsb repair and may link cell cycle checkpoints to HR activation.
Assuntos
Antígenos Nucleares , DNA Helicases , Reparo do DNA/genética , Proteínas Serina-Treonina Quinases/genética , Recombinação Genética , Animais , Ataxia Telangiectasia/genética , Proteínas Mutadas de Ataxia Telangiectasia , Proteínas Aviárias , Proteínas de Ciclo Celular , Divisão Celular/genética , Divisão Celular/efeitos da radiação , Linhagem Celular , Galinhas , Aberrações Cromossômicas/genética , Dano ao DNA/genética , Enzimas Reparadoras do DNA , Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/efeitos da radiação , Imunofluorescência , Proteínas Fúngicas/genética , Proteínas Fúngicas/efeitos da radiação , Marcação de Genes , Humanos , Immunoblotting , Autoantígeno Ku , Proteínas Nucleares/genética , Proteínas Nucleares/efeitos da radiação , Rad51 Recombinase , Tolerância a Radiação/genética , Proteínas de Saccharomyces cerevisiae , Proteínas Supressoras de TumorRESUMO
Yeast Mre11 functions with Rad50 and Xrs2 in a complex that has pivotal roles in homologous recombination (HR) and non-homologous end-joining (NHEJ) DNA double-strand break (DSB) repair pathways. Vertebrate Mre11 is essential. Conditionally, MRE11 null chicken DT40 cells accumulate chromosome breaks and die upon Mre11 repression, showing frequent centrosome amplification. Mre11 deficiency also causes increased radiosensitivity and strongly reduced targeted integration frequencies. Mre11 is, therefore, crucial for HR and essential in mitosis through its role in chromosome maintenance by recombinational repair. Surprisingly perhaps, given the role of Mre11 in yeast NHEJ, disruption of NHEJ by deletion of KU70 greatly exacerbates the effects of MRE11 deficiency, revealing a significant Mre11-independent component of metazoan NHEJ.
Assuntos
Cromossomos/genética , Reparo do DNA/genética , Endodesoxirribonucleases , Exodesoxirribonucleases , Proteínas Fúngicas/fisiologia , Proteínas de Saccharomyces cerevisiae , Animais , Proteínas Aviárias , Linfócitos B/efeitos da radiação , Ciclo Celular/efeitos da radiação , Linhagem Celular , Centrossomo/fisiologia , Galinhas , Aberrações Cromossômicas , Reparo do DNA/efeitos da radiação , Proteínas de Ligação a DNA/genética , Relação Dose-Resposta à Radiação , Imunofluorescência , Mutagênese Sítio-Dirigida , Plasmídeos , Rad51 Recombinase , Recombinação Genética/genética , Recombinação Genética/efeitos da radiação , Fatores de TempoRESUMO
Genetic recombination and the repair of double-strand DNA breaks in Saccharomyces cerevisiae require Rad51, a homologue of the Escherichia coli RecA protein. In vitro, Rad51 binds DNA to form an extended nucleoprotein filament and catalyzes the ATP-dependent exchange of DNA between molecules with homologous sequences. Vertebrate Rad51 is essential for cell proliferation. Using site-directed mutagenesis of highly conserved residues of human Rad51 (hRad51) and gene targeting of the RAD51 locus in chicken DT40 cells, we examined the importance of Rad51's highly conserved ATP-binding domain. Mutant hRad51 incapable of ATP hydrolysis (hRad51K-133R) binds DNA less efficiently than the wild type but catalyzes strand exchange between homologous DNAs. hRad51 does not need to hydrolyze ATP to allow vertebrate cell proliferation, form nuclear foci, or repair radiation-induced DNA damage. However, cells expressing hRad51K-133R show greatly reduced targeted integration frequencies. These findings show that ATP hydrolysis is involved in DNA binding by hRad51 and suggest that the extent of DNA complexed with hRad51 in nucleoprotein influences the efficiency of recombination.
Assuntos
Trifosfato de Adenosina/metabolismo , DNA Nucleotidiltransferases/metabolismo , Proteínas de Ligação a DNA/metabolismo , Sequência de Aminoácidos , Proteínas Aviárias , Sítios de Ligação/genética , Divisão Celular/efeitos da radiação , Sobrevivência Celular , Sequência Conservada , DNA Nucleotidiltransferases/genética , Reparo do DNA , Proteínas de Ligação a DNA/genética , Raios gama , Genes Essenciais , Teste de Complementação Genética , Humanos , Hidrólise , Mutagênese Sítio-Dirigida , Ligação Proteica , Rad51 RecombinaseRESUMO
Sister chromatid exchange (SCE) frequency is a commonly used index of chromosomal stability in response to environmental or genetic mutagens. However, the mechanism generating cytologically detectable SCEs and, therefore, their prognostic value for chromosomal stability in mitotic cells remain unclear. We examined the role of the highly conserved homologous recombination (HR) pathway in SCE by measuring SCE levels in HR-defective vertebrate cells. Spontaneous and mitomycin C-induced SCE levels were significantly reduced for chicken DT40 B cells lacking the key HR genes RAD51 and RAD54 but not for nonhomologous DNA end-joining (NHEJ)-defective KU70(-/-) cells. As measured by targeted integration efficiency, reconstitution of HR activity by expression of a human RAD51 transgene restored SCE levels to normal, confirming that HR is the mechanism responsible for SCE. Our findings show that HR uses the nascent sister chromatid to repair potentially lethal DNA lesions accompanying replication, which might explain the lethality or tumorigenic potential associated with defects in HR or HR-associated proteins.
Assuntos
Antígenos Nucleares , DNA Helicases , Troca de Cromátide Irmã , Animais , Proteínas Aviárias , Galinhas , Replicação do DNA , Proteínas de Ligação a DNA/genética , Humanos , Autoantígeno Ku , Proteínas Nucleares/genética , Rad51 RecombinaseRESUMO
Rad52 plays a pivotal role in double-strand break (DSB) repair and genetic recombination in Saccharomyces cerevisiae, where mutation of this gene leads to extreme X-ray sensitivity and defective recombination. Yeast Rad51 and Rad52 interact, as do their human homologues, which stimulates Rad51-mediated DNA strand exchange in vitro, suggesting that Rad51 and Rad52 act cooperatively. To define the role of Rad52 in vertebrates, we generated RAD52(-/-) mutants of the chicken B-cell line DT40. Surprisingly, RAD52(-/-) cells were not hypersensitive to DNA damages induced by gamma-irradiation, methyl methanesulfonate, or cis-platinum(II)diammine dichloride (cisplatin). Intrachromosomal recombination, measured by immunoglobulin gene conversion, and radiation-induced Rad51 nuclear focus formation, which is a putative intermediate step during recombinational repair, occurred as frequently in RAD52(-/-) cells as in wild-type cells. Targeted integration frequencies, however, were consistently reduced in RAD52(-/-) cells, showing a clear role for Rad52 in genetic recombination. These findings reveal striking differences between S. cerevisiae and vertebrates in the functions of RAD51 and RAD52.
Assuntos
Linfócitos B/metabolismo , Reparo do DNA/genética , Proteínas de Ligação a DNA/fisiologia , Recombinação Genética/genética , Animais , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Galinhas , Cisplatino/farmacologia , Proteínas de Ligação a DNA/genética , Imunofluorescência , Marcação de Genes , Imunoglobulina M/imunologia , Metanossulfonato de Metila/farmacologia , Mutagênicos/farmacologia , Transfecção/normas , Raios XRESUMO
To study the relative contributions of clonal deletion, clonal anergy, and receptor editing to tolerance induction in autoreactive B cells and their dependence on B cell receptor affinity, we have constructed "knock in" mice in which germline encoded or somatically mutated, rearranged anti-DNA heavy (H) chains were targeted to the H chain locus of the mouse. The targeted H chains were expressed on the vast majority of bone marrow (BM) and splenic B cells and were capable of Ig class switching and the acquisition of somatic mutations. A quantitative analysis of B cell populations in the BM as well as of Jkappa utilization and DNA binding of hybridoma Abs suggested that immature B cell deletion and light (L) chain editing were the major mechanisms affecting tolerance. Unexpectedly, these mechanisms were less effective in targeted mice expressing the somatically mutated, anti-DNA H chain than in mice expressing the germline-encoded H chain, possibly due to the greater abundance of high affinity, anti-DNA immature B cells in the BM. Consequently, autoreactive B cells that showed features of clonal anergy could be recovered in the periphery of these mice. Our results suggest that clonal deletion and receptor editing are interrelated mechanisms that act in concert to eliminate autoreactive B cells from the immune system. Clonal anergy may serve as a back-up mechanism for central tolerance, or it may represent an intermediate step in clonal deletion.
Assuntos
Anticorpos Antinucleares/genética , Linfócitos B/citologia , Anergia Clonal , Deleção Clonal , DNA/imunologia , Rearranjo Gênico de Cadeia Pesada de Linfócito B , Genes de Imunoglobulinas , Cadeias Pesadas de Imunoglobulinas/genética , Receptores de Antígenos de Linfócitos B/genética , Sequência de Aminoácidos , Animais , Antígenos Virais/imunologia , Autoantígenos/imunologia , Autoimunidade , Linfócitos B/imunologia , Sequência de Bases , Células da Medula Óssea/imunologia , Feminino , Marcação de Genes , Hibridomas/imunologia , Imunização , Switching de Imunoglobulina , Cadeias J de Imunoglobulina/genética , Região Variável de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Vírus da Influenza A/imunologia , Lipopolissacarídeos/farmacologia , Ativação Linfocitária/efeitos dos fármacos , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Camundongos Transgênicos , Dados de Sequência Molecular , Mutação , Reação em Cadeia da Polimerase , Alinhamento de Sequência , Homologia de Sequência , Baço/imunologiaRESUMO
Eukaryotic cells repair DNA double-strand breaks (DSBs) by at least two pathways, homologous recombination (HR) and non-homologous end-joining (NHEJ). Rad54 participates in the first recombinational repair pathway while Ku proteins are involved in NHEJ. To investigate the distinctive as well as redundant roles of these two repair pathways, we analyzed the mutants RAD54(-/-), KU70(-/-) and RAD54(-/-)/KU70(-/-), generated from the chicken B-cell line DT40. We found that the NHEJ pathway plays a dominant role in repairing gamma-radiation-induced DSBs during G1-early S phase while recombinational repair is preferentially used in late S-G2 phase. RAD54(-/-)/KU70(-/-) cells were profoundly more sensitive to gamma-rays than either single mutant, indicating that the two repair pathways are complementary. Spontaneous chromosomal aberrations and cell death were observed in both RAD54(-/-) and RAD54(-/-)/KU70(-/-) cells, with RAD54(-/-)/KU70(-/-) cells exhibiting significantly higher levels of chromosomal aberrations than RAD54(-/-) cells. These observations provide the first genetic evidence that both repair pathways play a role in maintaining chromosomal DNA during the cell cycle.