RESUMEN
Genetic experiments have determined that Ku, XRCC4, and ligase IV are required for repair of double-strand breaks by the end-joining pathway. The last two factors form a tight complex in cells. However, ligase IV is only one of three known mammalian ligases and is intrinsically the least active in intermolecular ligation; thus, the biochemical basis for requiring this ligase has been unclear. We demonstrate here a direct physical interaction between the XRCC4-ligase IV complex and Ku. This interaction is stimulated once Ku binds to DNA ends. Since XRCC4-ligase IV alone has very low DNA binding activity, Ku is required for effective recruitment of this ligase to DNA ends. We further show that this recruitment is critical for efficient end-joining activity in vitro. Preformation of a complex containing Ku and XRCC4-ligase IV increases the initial ligation rate 20-fold, indicating that recruitment of the ligase is an important limiting step in intermolecular ligation. Recruitment by Ku also allows XRCC4-ligase IV to use Ku's high affinity for DNA ends to rapidly locate and ligate ends in an excess of unbroken DNA, a necessity for end joining in cells. These properties are conferred only on ligase IV, because Ku does not similarly interact with the other mammalian ligases. We have therefore defined cell-free conditions that reflect the genetic requirement for ligase IV in cellular end joining and consequently can explain in molecular terms why this factor is required.
Asunto(s)
Antígenos Nucleares , ADN Helicasas , ADN Ligasas/metabolismo , Reparación del ADN , Proteínas de Unión al ADN/metabolismo , Proteínas de Unión al ADN/fisiología , ADN/metabolismo , Proteínas Nucleares/fisiología , Unión Competitiva , ADN Ligasa (ATP) , ADN Ligasas/aislamiento & purificación , ADN Complementario/metabolismo , Proteínas de Unión al ADN/aislamiento & purificación , Células HeLa , Humanos , Autoantígeno Ku , Pruebas de Precipitina , Unión Proteica , Factores de TiempoAsunto(s)
Antígenos Nucleares , ADN Helicasas , Reordenamiento Génico de Linfocito B , Reordenamiento Génico de Linfocito T , Recombinación Genética , Animales , Variación Antigénica , ADN/química , ADN/genética , ADN/metabolismo , Reparación del ADN/genética , Elementos Transponibles de ADN/genética , Proteínas de Unión al ADN/metabolismo , Proteínas de Homeodominio/metabolismo , Humanos , Autoantígeno Ku , Proteína Homóloga de MRE11 , Proteínas Nucleares/metabolismo , Conformación de Ácido Nucleico , Translocación GenéticaRESUMEN
Ku protein binds to DNA ends and is a cofactor for the DNA-dependent protein kinase. Both of these components are involved in DNA double-strand break repair, but it has not been clear if they function indirectly, by sensing DNA damage and activating other factors, or if they are more directly involved in the processing and rejoining of DNA breaks. We demonstrate that intermolecular ligation of DNA fragments is highly dependent on Ku under conditions designed to mimic those existing in the cell. This effect of Ku is specific to eukaryotic DNA ligases. Ku protein, therefore, has an activity consistent with a direct role in rejoining DNA breaks and independent of DNA-dependent protein kinase.
Asunto(s)
Antígenos Nucleares , Daño del ADN , ADN Helicasas , ADN Ligasas/fisiología , Reparación del ADN , Proteínas de Unión al ADN/fisiología , Proteínas Nucleares/fisiología , ADN/metabolismo , ADN Ligasa (ATP) , ADN Ligasas/metabolismo , Reparación del ADN/efectos de los fármacos , Humanos , Autoantígeno Ku , Proteínas de Unión a Poli-ADP-Ribosa , Proteínas de XenopusRESUMEN
V(D)J recombination generates diversity in the immune system through the lymphoid-specific assembly of multiple gene segments into functional immunoglobulin and T-cell receptor genes. The first step in V(D)J recombination is cleavage of DNA at recombination signal sequences. Cleavage produces a blunt DNA end on each signal sequence and a hairpin end on adjacent coding gene segments, and can be reproduced in vitro by using purified RAG and RAG2 proteins. The later steps involve processing and joining of the cleaved DNA ends, and until now have been studied only in cells. Here we reconstitute the complete V(D)J recombination reaction in a cell-free system. We find that the RAG proteins are not only involved in cleavage, but are also needed in the later steps for efficient joining of coding ends. Joining is largely directed by short pieces of identical sequence in the coding flanks, but addition of human DNA ligase I results in greater diversity. Coding junctions contain short deletions as well as additions complementary to a coding flank (P nucleotides). Addition of non-templated nucleotides into coding junctions is mediated by terminal deoxyribonucleotidyl transferase. The cell-free reaction can therefore reproduce the complete set of processing events that occur in cells.
Asunto(s)
Proteínas de Unión al ADN/fisiología , Proteínas de Homeodominio , Cadenas J de Inmunoglobulina/genética , Región Variable de Inmunoglobulina/genética , Recombinación Genética , Sistema Libre de Células , ADN Ligasa (ATP) , ADN Ligasas/metabolismo , Células HeLa , Humanos , Proteínas NuclearesRESUMEN
Recent in vitro work on V(D)J recombination has helped to clarify its mechanism. The first stage of the reaction, which can be reproduced with the purified RAG1 and RAG2 proteins, is a site-specific cleavage that generates the same broken DNA species found in vivo. The cleavage reaction is closely related to known types of transpositional recombination, such as that of HIV integrase. All the site specificity of V(D)J recombination, including the 12/23 rule, is determined by the RAG proteins. The later steps largely overlap with the repair of radiation-induced DNA double-strand breaks, as indicated by the identity of several newly characterized factors involved in repair. These developments open the way for a thorough biochemical study of V(D)J recombination.
Asunto(s)
Reordenamiento Génico/inmunología , Recombinación Genética/genética , Recombinación Genética/inmunología , Animales , HumanosRESUMEN
Cleavage of V(D)J recombination signals by purified RAG1 and RAG2 proteins permits the dissection of DNA structure and sequence requirements. The two recognition elements of a signal (nonamer and heptamer) are used differently, and their cooperation depends on correct helical phasing. The nonamer is most important for initial binding, while efficient nicking and hairpin formation require the heptamer sequence. Both nicking and hairpin formation are remarkably tolerant of variations in DNA structure. Certain flanking sequences inhibit hairpin formation, but this can be bypassed by base unpairing, and even a completely single-stranded signal sequence is well utilized. We suggest that DNA unpairing around the signal-coding border is essential for the initiation of V(D)J combination.
Asunto(s)
Proteínas de Unión al ADN , ADN/genética , Genes de Inmunoglobulinas , Proteínas de Homeodominio , Receptores de Antígenos de Linfocitos T/genética , Recombinación Genética , Transducción de Señal , Secuencia de Bases , Biopolímeros , Datos de Secuencia Molecular , Conformación de Ácido Nucleico , Proteínas/metabolismoRESUMEN
V(D)J recombination requires a pair of signal sequences with spacer lengths of 12 and 23 base pairs. Cleavage by the RAG1 AND RAG2 proteins was previously shown to demand only a single signal sequence. Here, we established conditions where 12- and 23-spacer signal sequences are both necessary for cleavage. Coupled cutting at both sites requires only the RAG1 and RAG2 proteins, but depends on the metal ion. In Mn2+, a single signal sequence supports efficient double strand cleavage, but cutting in Mg2+ requires two signal sequences and is best with the canonical 12/23 pair. Thus, the RAG proteins determine both aspects of the specificity of V(D)J recombination, the recognition of a single signal sequence and the correct 12/23 coupling in a pair of signals.
Asunto(s)
Proteínas de Unión al ADN , Reordenamiento Génico/genética , Proteínas de Homeodominio , Proteínas/genética , Animales , Secuencia de Bases , Cationes/farmacología , Reordenamiento Génico/efectos de los fármacos , Genes de Insecto/genética , Insectos , Cinética , Datos de Secuencia Molecular , Análisis de Secuencia de ADNRESUMEN
Mouse VH gene segments are conventionally classified into 13 families on the basis of sequence similarity. The 7183 family lies close to the 3' end of the locus and is preferentially used in BALB/c mice; J558, the largest family, lies close to the 5' end of the VH stretch and is preferentially used in C57BL/6 mice. To investigate whether differential effectiveness of the RSSs in the two families might contribute to the overusage of 7183 in the primary repertoire of BALB/c, we constructed recombination substrates in which the recombination signal sequences (RSSs) of VH segments 7183 and J558 compete with each other for a single RSS, DFL16.1, after transfection into two transformed cell lines derived from C57BL/6 and two cell lines from BALB/c mice. In both strains, the 7183 RSS was found to be preferentially used (83%). Thus, the 7183 RSS mediates recombination more frequently than does that of J558, and this preference must thereby influence the primary repertoire, but the strain difference cannot be accounted for by a difference in the RSSs.
Asunto(s)
Reordenamiento Génico de Cadena Pesada de Linfocito B , Cadenas Pesadas de Inmunoglobulina/genética , Región Variable de Inmunoglobulina/genética , Animales , Secuencia de Bases , Línea Celular , ADN , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Datos de Secuencia MolecularRESUMEN
Formation of double-strand breaks at recombination signal sequences is an early step in V(D)J recombination. Here we show that purified RAG1 and RAG2 proteins are sufficient to carry out this reaction. The cleavage reaction can be divided into two distinct steps. First, a nick is introduced at the 5' end of the signal sequence. The other strand is then broken, resulting in a hairpin structure at the coding end and a blunt, 5'-phosphorylated signal end. The hairpin is made as a direct consequence of the cleavage mechanism. Nicking and hairpin formation each require the presence of a signal sequence and both RAG proteins.
Asunto(s)
Proteínas de Unión al ADN , Genes RAG-1/fisiología , Proteínas de Homeodominio , Proteínas/genética , Secuencia de Aminoácidos , Secuencia de Bases , ADN/metabolismo , Células HeLa/fisiología , Humanos , Datos de Secuencia Molecular , Proteínas Nucleares , Conformación de Ácido Nucleico , Señales de Clasificación de Proteína/genética , Proteínas/aislamiento & purificación , Proteínas/metabolismo , Recombinación GenéticaRESUMEN
A recently described pre-B cell line can be induced at high temperature to actively rearrange its immunoglobulin light-chain loci. We used this cell line to determine the fate of double-strand breaks generated by V(D)J rearrangement. After induction, 30%-40% of K loci had broken JK1 signal ends. JK1-coding ends were detectable, but 10- to 100-fold less frequent. Both covalently closed (hairpin) and open, blunt, processed coding ends were observed. Coding junctions involving JK1 accumulated with similar kinetics as JK1 signal ends, arguing that coding ends can be resolved quickly and efficiently to coding junctions, whereas signal ends remain mostly unjoined. Signal ends are then joined rapidly when cells are returned to the low temperature. These results support the model that broken signal ends and hairpin coding ends are authentic intermediates in V(D)J recombination. It appears that hairpin coding ends are rapidly opened, processed, and resolved to coding junctions, whereas joining of signal ends is clearly uncoupled from the joining of coding ends and can be much slower. Efficient formation of signal junctions may require cell cycle progression, or down-regulation of the recombination machinery.
Asunto(s)
Linfocitos B/inmunología , Reordenamiento Génico de Linfocito B , Genes de Inmunoglobulinas/genética , Recombinación Genética , Animales , Secuencia de Bases , Southern Blotting , Línea Celular , ADN/metabolismo , ADN Nucleotidiltransferasas/metabolismo , Electroforesis en Gel de Agar , Electroforesis en Gel Bidimensional , Calor , Región de Unión de la Inmunoglobulina/genética , Región Variable de Inmunoglobulina/genética , Cadenas kappa de Inmunoglobulina/genética , Ratones , Ratones Endogámicos BALB C , Datos de Secuencia Molecular , Transformación Genética/genética , VDJ RecombinasasRESUMEN
Cells performing V(D)J recombination make specific cuts in DNA at recombination signal sequences. Here, we show that nuclear extracts of pre-B cell lines carry out this specific cleavage. The products of cleavage are the same as found previously in thymocytes: full-length, blunt, 5'-phosphorylated signal ends, and covalently sealed (hairpin) coding ends. A complete signal sequence is required. Recombinant RAG1 protein greatly increases activity and complements an inactive extract from a RAG1 (-/-) pre-B cell line. When the extracts are fractionated, cleavage activity correlates with the presence of RAG2 protein. These results suggest that RAG1 and RAG2 are components of the V(D)J recombinase.
Asunto(s)
Proteínas de Unión al ADN , Genes de Inmunoglobulinas , Proteínas de Homeodominio , Receptores de Antígenos de Linfocitos T/genética , Recombinación Genética , Animales , Linfocitos B/inmunología , Secuencia de Bases , Línea Celular , Sistema Libre de Células , ADN/genética , Cartilla de ADN/genética , Datos de Secuencia Molecular , Proteínas/genéticaRESUMEN
Ig variable domains are generated by the recombination of V, D, and J segments (V(D)J rearrangement). V(D)J rearrangement is capable of generating a vast repertoire of different variable domains. In this report, we quantify and characterize the repertoire of kappa rearrangements in fetal liver ontogeny. VJ kappa rearrangements are first observable at approximately day 14 of gestation. Characterization of these rearrangements indicates that only 33% are in a productive reading frame, which supports the argument that they have been generated recently and have not as yet undergone significant Ag-driven selection. Further analysis of rearrangements from a pool of 133 cloned VJ kappa junctions (from both day 14 and day 16 of gestation) indicates that the repertoire is fairly diverse with respect to the V kappa gene families used, as well as the number of members from each gene family. The frequency of V kappa 4 family use in rearrangements to J kappa 5, however, was approximately twice that of the frequency of V kappa 4 family use in rearrangement to other J kappa s. The fine structure of fetal VJ kappa junctions was also diverse, which indicates that precise deletion of sequence identities shared between rearranging V kappa J kappa pairs does not significantly reduce junctional diversity, as has been observed in DJH rearrangements. Lastly, a number of junctions contained P nucleotides, in contrast to the repertoire of expressed VJ kappa junctions.
Asunto(s)
Reordenamiento Génico de Cadena Ligera de Linfocito B , Cadenas kappa de Inmunoglobulina/genética , Animales , Diversidad de Anticuerpos , Secuencia de Bases , Cartilla de ADN/química , Genes de Inmunoglobulinas , Edad Gestacional , Hígado/embriología , Ratones , Ratones Endogámicos C57BL , Datos de Secuencia MolecularRESUMEN
The variable domains of immunoglobulins and T cell receptors are assembled through the somatic, site specific recombination of multiple germline segments (V, D, and J segments) or V(D)J rearrangement. The recombination signal sequence (RSS) is necessary and sufficient for cell type specific targeting of the V(D)J rearrangement machinery to these germline segments. Previously, the RSS has been described as possessing both a conserved heptamer and a conserved nonamer motif. The heptamer and nonamer motifs are separated by a 'spacer' that was not thought to possess significant sequence conservation, however the length of the spacer could be either 12 +/- 1 bp or 23 +/- 1 bp long. In this report we have assembled and analyzed an extensive data base of published RSS. We have derived, through extensive consensus comparison, a more detailed description of the RSS than has previously been reported. Our analysis indicates that RSS spacers possess significant conservation of sequence, and that the conserved sequence in 12 bp spacers is similar to the conserved sequence in the first half of 23 bp spacers.
Asunto(s)
Secuencia Conservada , Reordenamiento Génico/genética , Genes de Inmunoglobulinas/genética , Receptores de Antígenos de Linfocitos T/genética , Recombinación Genética/genética , Animales , Diversidad de Anticuerpos , Composición de Base , Secuencia de Bases , Secuencia de Consenso , ADN/genética , Humanos , Datos de Secuencia Molecular , Alineación de SecuenciaAsunto(s)
Linfocitos B/fisiología , Células Madre Hematopoyéticas/fisiología , Tejido Linfoide/fisiología , Animales , Diferenciación Celular , Factores Estimulantes de Colonias , Reordenamiento Génico de Linfocito B/fisiología , Genes de Inmunoglobulinas/fisiología , Humanos , Hígado/embriología , Hígado/fisiología , Modelos BiológicosAsunto(s)
Linfocitos B/inmunología , Regulación de la Expresión Génica/inmunología , Cadenas kappa de Inmunoglobulina/biosíntesis , Cadenas lambda de Inmunoglobulina/biosíntesis , Animales , Secuencia de Bases , Reordenamiento Génico de Cadena Ligera de Linfocito B , Genes de Inmunoglobulinas/fisiología , Genotipo , Cadenas kappa de Inmunoglobulina/genética , Cadenas lambda de Inmunoglobulina/genética , Ratones , Modelos Genéticos , Datos de Secuencia MolecularRESUMEN
Immunoglobulin and T-cell receptor genes are somatically rearranged by site-specific recombination. Recombination signal sequences (RSS) have been identified as the major targeting element of this process. Recent reports demonstrate that differences in RSS affect the frequency of recombination, suggesting a role for RSS in the development of the B-cell repertoire. Examination of mouse light-chain RSS indicates that kappa light-chain RSS consistently show a greater degree of similarity to a consensus sequence than do those of lambda light chain. To determine whether this difference in natural RSS could affect the patterns of light-chain gene rearrangement and expression, we have constructed recombination substrates containing both a typical mouse kappa RSS pair and a typical mouse lambda RSS pair. Experiments using these substrates demonstrate that the kappa RSS pair mediates recombination at a vastly higher frequency than does the lambda RSS pair. This result argues that RSS differences may contribute significantly to the patterns of mouse immunoglobulin light-chain rearrangement, ultimately resulting in a high proportion of kappa light chain relative to lambda.
Asunto(s)
ADN Nucleotidiltransferasas/metabolismo , Cadenas Ligeras de Inmunoglobulina/genética , Cadenas kappa de Inmunoglobulina/genética , Cadenas lambda de Inmunoglobulina/genética , Señales de Clasificación de Proteína/genética , Recombinación Genética , Animales , Secuencia de Bases , Línea Celular , Reordenamiento Génico , Ratones , Datos de Secuencia Molecular , Oligodesoxirribonucleótidos , Plásmidos , Homología de Secuencia de Ácido Nucleico , VDJ RecombinasasRESUMEN
In this review, we have assembled some results on VH gene usage by mouse and human. We conclude that there is an early bias in usage of certain VH genes in both mouse and human. This biased usage has a strain dependent component as evidenced by its continued presence in the adult repertoire of some mouse strains, notably BALB/c, and not in others. The reason for the fetal bias is uncertain. However, the finding that the VH gene segments used in the human fetal repertoire are similar in sequence but not in chromosomal position to those expressed in the mouse fetal-repertoire leads us to suggest that the bias is not due to chromosomal location but rather may be reflecting the functioning of these gene products early in ontogeny.
Asunto(s)
Genes de Inmunoglobulinas , Cadenas Pesadas de Inmunoglobulina/genética , Región Variable de Inmunoglobulina/genética , Ratones/inmunología , Animales , Mapeo Cromosómico , Embrión de Mamíferos/inmunología , Feto/inmunología , Regulación de la Expresión Génica , Humanos , Recombinación GenéticaRESUMEN
Autoantibodies that bind aminoacyl-tRNA synthetases are strongly associated with the human inflammatory myopathies polymyositis and dermatomyositis, but their molecular origins and relationship to pathogenesis are not known. To address these issues, we wished to identify the autoantigenic epitopes which react with these autoantibodies and to this end, we previously isolated a full length cDNA clone encoding the target Ag recognized most frequently by myositis sera, histidyl-tRNA synthetase (HRS). In the present study, we have analyzed the HRS autoepitopes by two amino acid insertion linker mutagenesis of HRS proteins expressed in Cos 1 cells. A series of mutant HRS cDNA were constructed and the expressed proteins were tested for enzyme activity and for immune reactivity with a panel of sera with anti-Jo-1 antibodies. Immunoblotting and immunoprecipitation analyses revealed that anti-Jo-1 antibodies recognize multiple conformation-dependent and independent epitopes on HRS and that the autoepitopes vary among different myositis patients.