RESUMO
Besides its well-established role in wound healing and fibrinolysis, tissue-type plasminogen activator (t-PA) has been shown to contribute to cognitive processes and memory formation within the central nervous system, and to promote glutamate receptor-mediated excitotoxicity. The t-PA gene is expressed and regulated in neuronal cells but the regulatory transcriptional processes directing this expression are still poorly characterized. We have used DNase I-hypersensitivity mapping and in vivo foot printing to identify putative regulatory elements and transcription factor binding sites in two human neuroblastomal (KELLY and SK-N-SH) and one human glioblastomal (SNB-19) cell lines. Hypersensitive sites were found in the proximal promoter region of all cell lines, and within the first exon for KELLY and SNB-19 cells. Mapping of methylation-protected residues in vivo detected a cluster of protected residues corresponding to a cAMP response element (CRE) and Sp1 sites in the proximal promoter previously shown to be essential for basal expression in other cell types. Protected residues were also found at other sites, notably a kappaB element at position bp -3081 to -3072 that was partly protected in KELLY and SNB-19 cells. Analysis of transfected reporter constructs in KELLY and SNB-19 cells confirmed that this particular element is functionally significant in the transactivation of the t-PA promoter in both cell types. This study defines, by in vivo and in vitro methods, a previously undescribed kappaB site in the t-PA gene promoter that influences t-PA expression in neuronal cells.
Assuntos
Neuroblastoma/genética , Regiões Promotoras Genéticas , Ativador de Plasminogênio Tecidual/genética , Linhagem Celular Tumoral , Cromatina/metabolismo , AMP Cíclico/metabolismo , DNA/metabolismo , Desoxirribonuclease I/metabolismo , Endotélio Vascular/metabolismo , Genes Reporter , Células HeLa , Humanos , Técnicas In Vitro , Luciferases/metabolismo , Memória , Metilação , Modelos Biológicos , Família Multigênica , NF-kappa B/metabolismo , Neurônios/metabolismo , Ésteres de Forbol/metabolismo , Reação em Cadeia da Polimerase , Ligação Proteica , Elementos de Resposta , Fator de Transcrição Sp1/metabolismo , Transcrição Gênica , TransfecçãoRESUMO
An 80,000 base-pair region from the gene locus encoding the variable regions of the human immunoglobulins of the kappa type (V kappa genes) was cloned and analysed. The region comprises five V kappa sequences of subgroup I and one interspersed V kappa pseudogene of subgroup II. The six genes and pseudogenes are arranged at different distances but in the same orientation. The organization of the cluster can be explained by a series of amplification steps; the existence of a V kappa II pseudogene in a V kappa I gene cluster may have been the result of a transposition event; a final duplication step led to a second closely related copy of the cluster. From sequence data for altogether 16,000 base-pairs it appears that gene conversion-like events and subsequent selection contribute to both homogeneity and diversity of the V kappa repertoire.
Assuntos
Genes , Cadeias Leves de Imunoglobulina/genética , Região Variável de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Sequência de Aminoácidos , Diversidade de Anticorpos , Composição de Bases , Sequência de Bases , Evolução Biológica , Mapeamento Cromossômico , Enzimas de Restrição do DNA , Amplificação de Genes , HumanosRESUMO
Immunophenotypes and Ig gene rearrangements were investigated in 12 patients with a variant form of hairy cell leukemia (HCL) termed HCL-Japanese variant (HCL-J), and in an HCL-J-derived cell line. The leukemic cells of HCL-J characteristically showed the phenotype of CD20+, CD5-, CD10-, CD11c+, CD22+, CD24- and CD25-. Ig light (L) chain was undetected in nine cases, and the remaining four cases expressed kappa chain. Expression of Ig heavy (H) chain was studied in nine cases. In addition to Igkappa+ cases showing expression of predominantly gamma H chain isotype, alpha chain was detected in one case without expression of L chain. Rearranged bands in Ig heavy chain (JH) genes were recognized in all 12 cases tested. Rearranged bands in kappa chain genes and germline configuration in chi chain genes were seen in all three Igkappa+ cases tested. Four of nine cases without expression of L chain had a rearranged chi chain gene. The other three cases had chi chain genes in the germline configuration and rearranged and/or deleted kappa chain genes. In the remaining two cases, no rearrangement in either kappa or chi chain genes was detected. The Ig gene configuration and expression in HCL-J, partially overlapping with those described for immature B cell leukemia, were dissociated from the cytological features and CD20+, membrane CD22+ phenotype characteristic of mature B cells.
Assuntos
Antígenos CD/sangue , Rearranjo Gênico , Genes de Imunoglobulinas , Leucemia de Células Pilosas/genética , Leucemia de Células Pilosas/imunologia , Anticorpos Monoclonais , Linhagem Celular , Fluoresceína-5-Isotiocianato , Técnica Direta de Fluorescência para Anticorpo , Variação Genética , Humanos , Cadeias Pesadas de Imunoglobulinas/genética , Cadeias Leves de Imunoglobulina/genética , Imunofenotipagem/métodos , Japão , Leucemia de Células Pilosas/sangue , Ficoeritrina , Células Tumorais CultivadasRESUMO
The element which mediates the deletion of the CK gene segment (abbreviations ref. 1) in human lambda light chain producing B-cells was found to be located 24 kb downstream of CK. The kappa deleting element is flanked by hepta- and nonanucleotide recognition sequences similar to the ones adjacent to the JK gene segments. Complementary recognition sequences with a 30 bp spacer were found in the JK-CK intron. For the first time the two partners of a recombination event in a mammalian immunoglobulin gene system have been linked on a physical map. The orientation of the recombination signals of the intron and the Kde sequences allows a joining by a simple deletion mechanism. Similarities and possible differences to the mechanism of V-J joining are discussed.
Assuntos
Deleção Cromossômica , Regiões Constantes de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Imunoglobulinas/genética , Linhagem Celular , Mapeamento Cromossômico , Regulação da Expressão Gênica , Ligação Genética , Humanos , Cadeias lambda de Imunoglobulina/genética , Recombinação GenéticaRESUMO
We have cloned a region of 124 kb of the human immunoglobulin lambda light chain locus on chromosome 22 encompassing seven V lambda and seven J-C lambda gene segments. No further C lambda gene segment was found in a region of 35 kb downstream of C lambda 7, which encodes the Ke+Oz- isotype. The C lambda proximal V lambda gene segment V lambda III. 1 is located 14.5 kb upstream of C lambda 1. The five sequenced V lambda genes have the same transcriptional orientation as the J-C lambda gene segments which is likely to be true for the majority of the V lambda gene segments in the human lambda locus and which suggests a deletion mechanism for DNA rearrangement. This is supported by hybridization of V lambda gene probes to germ-line and rearranged DNA from lambda light chain-producing cell lines. Sequences of 23 cDNA clones allow to establish a V lambda subgroup classification based on nucleic acid sequence data and an estimate of the J-C lambda usage.
Assuntos
Deleção Cromossômica , Mapeamento Cromossômico , Rearranjo Gênico , Genes de Imunoglobulinas , Regiões Constantes de Imunoglobulina/genética , Região de Junção de Imunoglobulinas/genética , Cadeias Leves de Imunoglobulina/genética , Região Variável de Imunoglobulina/genética , Cadeias lambda de Imunoglobulina/genética , Sequência de Aminoácidos , Sequência de Bases , Clonagem Molecular , DNA/análise , Humanos , Dados de Sequência Molecular , Mutação , PseudogenesRESUMO
During B cell development, the onset of DNA rearrangements, expression, and somatic hypermutation of Ig genes are regulated through the complex interaction of cis-acting elements with trans-acting factors. Our aim is to identify DNA elements required during activation of the human Ig lambda light chain genes. Determination of deoxyribonuclease (DNase) I-hypersensitive sites in complex regulated genes can lead to the identification of sequence elements which would have been overlooked by employing transient transfection protocols. We have therefore investigated the chromatin structure of human J-C lambda genes and identified three DNase I-hypersensitive sites (HSS-1, -2, and -3) within an 8-kb region downstream of the J-C lambda 7 gene. HSS-2 and HSS-3 are B cell specific. The DNase I-hypersensitive sites are also present in kappa-producing cell lines which have not rearranged the Ig lambda locus and produce germ-line J-C lambda transcripts. We conclude that in mature B cells, both kappa and lambda loci are in an active structure regardless of the type of light chain they produce. This suggests that the chromatin structure of both loci is opened early in B cell development and that the active structure persists in mature B cells. The observed temporal order (first kappa, then lambda) of activation can be explained by consecutive synthesis of the appropriate regulating factors and the tight regulation of the recombination machinery through the products of L chain gene rearrangements.
Assuntos
Desoxirribonuclease I/genética , Genes de Imunoglobulinas , Regiões Constantes de Imunoglobulina/genética , Cadeias lambda de Imunoglobulina/genética , Família Multigênica , Sequência de Bases , Rearranjo Gênico do Linfócito B/imunologia , Humanos , Região de Junção de Imunoglobulinas/genética , Cadeias kappa de Imunoglobulina/genética , Dados de Sequência Molecular , Especificidade de Órgãos/genética , Especificidade de Órgãos/imunologia , Transcrição Gênica/imunologiaRESUMO
V kappa genes of man can recombine with the J kappa gene segments either by an inversion or by a deletion mechanism. Back-to-back fusion products of the respective recombination signal sequences (signal joints) are retained on the chromosome after the formation of a V kappa-J kappa coding joint by an inversion. Our knowledge of the structure of the human kappa locus and the application of the polymerase chain reaction allowed us now to establish a direct relationship between different kappa recombination products in the lymphoid cell line JI. Two consecutive inversions fully explain the existence of two coding joints and two signal joints on the same chromosome of this cell line. Although the initially formed coding joint is productively rearranged and expressed, a second V kappa-J kappa rearrangement took place which leads to an aberrant joint. In this process a J kappa gene segment of the signal joint that had been created in the first V kappa-J kappa joining was used as the recombination target. The sequence of the two rearrangements is unequivocal since a product of the first (productive) reaction is a partner in the second (aberrant) one.
Assuntos
Região de Junção de Imunoglobulinas/genética , Região Variável de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Recombinação Genética , Sequência de Aminoácidos , Sequência de Bases , Linfoma de Burkitt/genética , Linhagem Celular , Inversão Cromossômica , Cromossomos Humanos Par 2 , Rearranjo Gênico , Humanos , Dados de Sequência Molecular , Sondas de Oligonucleotídeos , Reação em Cadeia da Polimerase , Mapeamento por Restrição , Homologia de Sequência do Ácido NucleicoRESUMO
A detailed molecular analysis of both reciprocal recombination products of the variant t(2;8) chromosomal translocation of the Burkitt lymphoma derived cell line JI and their germline counterparts was carried out. The breakpoint on chromosome 8 is localized 28 kb to the 3' side of the c-myc protooncogene, the breakpoint on chromosome 2 was found to be within an aberrantly rearranged VK gene (abbreviations ref. 1). Novel features of the immunoglobulin moiety involved in this process include insertion of extra nucleotides in the V-J junction which have the characteristics of a N segment as it has been found up to now only in heavy chain and T cell receptor genes; the occurrence of somatic mutations in 8q+ and not in 2p-. These data allow a reconstruction of the course of events in the cell line JI; remarkable sequence regularities at the chromosomal breakpoints consisting of symmetrically placed dinucleotides and elements related to the hepta- and nonanucleotide recombinase recognition sequences are discussed in the context of the translocation mechanism.
Assuntos
Cromossomos Humanos Par 2/ultraestrutura , Cromossomos Humanos Par 8/ultraestrutura , Região Variável de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Mutação , Proteínas Proto-Oncogênicas/genética , Translocação Genética , Sequência de Bases , Linfoma de Burkitt/genética , Linhagem Celular , Mapeamento Cromossômico , DNA Nucleotidiltransferases/fisiologia , Genes , Humanos , Proteínas de Neoplasias/genética , Proteínas Proto-Oncogênicas c-myc , Recombinação Genética , VDJ RecombinasesRESUMO
DNA digests of 16 human lymphoid cell lines were studied in blot hybridization experiments with probes from V kappa genes and their immediate neighborhood as well as with single or low-copy probes from intergenic regions. The patterns were compared with those of placenta DNA digests in which the kappa genes are in the germline configuration. The differences of patterns which were detected with the first type of hybridization probes can be attributed to V kappa--J kappa rearrangements or to restriction site polymorphisms between individuals. Some of the pattern differences observed with the second type of probes can be interpreted best as arising from deletions of parts of the kappa locus. Such deletions may be individual variations but they may also be caused by the V kappa-J kappa rearrangement process. The results obtained with one particular probe which was derived from a nonduplicated part of the kappa locus allow some conclusions as to the mechanism of the V kappa--J kappa rearrangement: the genomic situation in some lymphoid cell lines can be explained by an inversion while in other cell lines clearly deletions have occurred. The observations are in agreement with the inversion-deletion mechanism of V kappa--J kappa rearrangement as proposed by Lewis et al. (1982, 1984).
Assuntos
Região Variável de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Alelos , Linhagem Celular , DNA/genética , Enzimas de Restrição do DNA , Eletroforese em Gel de Poliacrilamida , Humanos , Região de Junção de Imunoglobulinas/genética , Tecido Linfoide , Hibridização de Ácido NucleicoRESUMO
The 23-kb region between the V kappa and J kappa gene clusters was investigated in some detail. The region was found to be free of V kappa genes or V kappa gene-like structures, confirming the previous supposition that the V kappa gene B3 is the J kappa proximal V kappa gene. The B3-J kappa distance of 23 kb was found to be the same in the DNAs of several individuals. A HindIII restriction fragment length polymorphism was detected within this region. A sequence of 533 bp located approximately in the middle of the region has a highly homologous counterpart (called homox) on another chromosome. The two sequences are 96% identical. Possible mechanisms for the generation of such a duplicate are discussed.
Assuntos
Genes de Imunoglobulinas/genética , Regiões Constantes de Imunoglobulina/genética , Região Variável de Imunoglobulina/genética , Sequência de Bases , Clonagem Molecular , Desoxirribonuclease HindIII , Humanos , Dados de Sequência Molecular , Hibridização de Ácido Nucleico , Polimorfismo de Fragmento de Restrição , Mapeamento por Restrição , Homologia de Sequência do Ácido NucleicoRESUMO
The immunoglobulin heavy chain 3' enhancer may be a novel type of a transcriptional regulation element in as much as its function is position dependent. We show that there are interactions between the mu intron and 3' enhancer which are differentially regulated depending on the distance between the two elements. Thus, a transcriptional repression is exerted by the 3' enhancer when juxtaposed to the intron enhancer. Whereas no or only modest synergism between the immunoglobulin mu intron and 3' enhancer has been reported to date, we show here that the stimulatory effect is substantially increased by extending the distance between the two enhancers. In our stable expression system, the mu intron enhancer insulated the test gene from neighboring chromatin.
Assuntos
Elementos Facilitadores Genéticos/genética , Regulação da Expressão Gênica/genética , Cadeias Pesadas de Imunoglobulinas/genética , Imunoglobulina M/genética , Íntrons/genética , Animais , Regulação para Baixo/genética , Vetores Genéticos/genética , Camundongos , Ratos , Transcrição Gênica/genética , Transfecção , Regulação para Cima/genéticaRESUMO
The genetic basis of the antibody repertoire--estimated to exceed 10(6) different immunoglobulin molecules--is a major unanswered problem. The number of germ-line V kappa genes in the mouse genome is probably several hundred while the corresponding number for three out of four human V kappa subgroups (V kappa I, V kappa III and V kappa IV) is probably altogether only 15-20 (ref. 5). The kappa II proteins differ significantly in sequence from the other kappa-chain proteins. To determine the contribution of V kappa II genes to kappa-chain diversity, we searched for a human lymphoid cell line which produces a kappa II chain and report here for the first time the sequence of a V kappa II gene. According to blot hybridizations with this V kappa gene as a probe, subgroup II contributes about half as many genes to the V kappa gene repertoire as are detected by a V kappa I probe. Therefore the repertoire is rather small which implies that somatic mutations or other mechanisms must play an important role in the generation of light-chain diversity in humans.
Assuntos
Genes , Variação Genética , Cadeias Leves de Imunoglobulina/genética , Região Variável de Imunoglobulina/genética , Sequência de Aminoácidos , Sequência de Bases , Linhagem Celular , Enzimas de Restrição do DNA , Humanos , Linfócitos/imunologia , Hibridização de Ácido NucleicoRESUMO
As a first step in our studies of functionally rearranged K genes of man we cloned the germline JK-CK region from placenta DNA employing a mouse JK clone as hybridization probe. Subclones of the human JK-CK region were then used to characterize and clone the rearranged K genes of the lymphoid cell lines Walker and Daudi. The Walker cell line contains one rearranged and one germline K allele (K+,KO; ref. 1). Only one K gene was found in Daudi cells (K+). Restriction mapping and DNA sequencing showed, that the rearranged K genes from both cell lines are closely related. These features make the two cell lines particularly suitable for studies on the chromatin structure of K light chain genes. The 5' flanks of the two genes (388 bp) are identical while there is a 12% divergence between the VK gene segments themselves. This situation may reflect somatic mutation processes and/or gene conversion like events.
Assuntos
Genes , Cadeias Leves de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Sequência de Aminoácidos , Bacteriófago lambda/genética , Sequência de Bases , Linfoma de Burkitt/imunologia , Linhagem Celular , Clonagem Molecular , Enzimas de Restrição do DNA , DNA de Neoplasias/genética , Feminino , Humanos , Placenta/imunologia , GravidezRESUMO
The human lymphoid cell lines Walker and Daudi constitute a particularly suitable system for studies on the chromatin structure of K light chain genes (see preceding paper). The rearranged and non-rearranged alleles of Walker cells were found to be about equally sensitive towards digestion with DNAase I. A DNAase I hypersensitive site was mapped 0.13 kb upstream of the leader segment of the rearranged VK genes; it comprises a region in which promoter-like regulatory elements were discovered recently. Additional hypersensitive sites are located further upstream. A hypersensitive site in the JK-CK intron coincides with a putative tissue specific enhancer element. A hypersensitive region down-stream of CK overlaps with the cleavage/polyadenylation recognition signal which is flanked by sequences related to the above mentioned putative regulatory sequences. The coincidence between DNAase I hypersensitive sites and those sequences may be functionally significant.
Assuntos
Desoxirribonuclease I/metabolismo , Genes , Cadeias Leves de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Sequência de Bases , Linfoma de Burkitt/imunologia , Linhagem Celular , Núcleo Celular/análise , Enzimas de Restrição do DNA , DNA de Neoplasias/isolamento & purificação , Células HeLa/imunologia , Humanos , Hibridização de Ácido NucleicoRESUMO
V(D)J rearrangement, high level expression and somatic hypermutation of assembled Ig genes is tightly controlled by a number of regulatory sequence elements located in the vicinity of the J-, (D)-, and C-gene segments. During B cell maturation these elements become accessible to binding of trans-acting factors, reflecting the opening of the chromatin structure through an as yet unidentified mechanism. The mapping of regions of an altered chromatin structure (DNase I hypersensitivity) therefore is a powerful approach in identifying regulatory sequence elements. We here show that the human Ig lambda enhancer consists of three modules previously identified by us as DNase I-hypersensitive sites HSS-1, -2, and -3. The three sequence elements synergize in transcriptional activation of a reporter gene and together constitute a powerful tissue-specific enhancer which is a much stronger transcriptional activator than the kappa enhancers alone or in combination. We further show that the accessibility of the kappa and lambda enhancer elements for DNase I in the chromatin of a pre-B cell line (207) correlates with the transcriptional enhancer activities of kappa and lambda enhancer constructs. This finding is in support of an ordered model for Ig light chain activation (kappa before lambda).
Assuntos
Linfócitos B/imunologia , Elementos Facilitadores Genéticos/genética , Genes de Imunoglobulinas , Cadeias lambda de Imunoglobulina/genética , Transcrição Gênica , Linhagem Celular , Elementos Facilitadores Genéticos/imunologia , Rearranjo Gênico do Linfócito B , Humanos , Cadeias lambda de Imunoglobulina/imunologia , Ativação TranscricionalRESUMO
The synthetic androgen mibolerone elicits a set of distinct changes in the behaviour of an androgen responsive human prostatic carcinoma cell line (LNCaP). Inhibition of cell proliferation, induction of morphological change and of a prostate specific mRNA, and inhibition of colony formation in soft agar are induced by very low concentrations of mibolerone. The natural androgen dihydrotestosterone is much less effective. The changes in growth characteristics and morphology are reverted by excess antiandrogen, i.e. cyproterone acetate or hydroxyflutamide. Cell lines lacking androgen receptors (PC-3, DU 145 and MRC-5) are completely unresponsive to mibolerone. Taken together, our results indicate androgen receptor mediated suppression of the transformed phenotype in LNCaP cells.
Assuntos
Androgênios/farmacologia , Nandrolona/análogos & derivados , Neoplasias da Próstata/patologia , Antagonistas de Androgênios/farmacologia , Divisão Celular/efeitos dos fármacos , Transformação Celular Neoplásica , Ciproterona/análogos & derivados , Ciproterona/farmacologia , Acetato de Ciproterona , Di-Hidrotestosterona/farmacologia , Flutamida/análogos & derivados , Flutamida/farmacologia , Humanos , Masculino , Nandrolona/farmacologia , Neoplasias da Próstata/metabolismo , RNA Mensageiro/metabolismo , Receptores Androgênicos/fisiologia , Células Tumorais CultivadasRESUMO
The genes of the immunoglobulin kappa light chains are assembled during B-cell differentiation by somatic recombination of one of the V kappa (variable) gene segments and the J kappa-C kappa (joining-constant) gene region. This seems to occur by deletion of the DNa between V kappa and J kappa-C kappa if they are arranged in germ-line DNA in the same transcriptional polarity or by inversion of a fragment containing the V kappa gene if the polarities are opposite. We have cloned 75 V kappa genes and pseudogenes of the human kappa locus and linked them in large contigs. There seem to be no more than 85 such genes, less than 50 of these being potentially functional. Thirty-eight of the cloned genes have the same transcriptional polarity as J kappa-C kappa and are part of the so-called J kappa proximal cluster; 35 genes in a distal cluster (the result of a duplication event in evolution) have a polarity that was suggested to be opposite to the one of J kappa-C kappa. We now show that the V kappa genes of the proximal cluster rearrange by a deletion mechanism whereas the others join J kappa-C kappa by inversion of megabase-sized DNA fragments.
Assuntos
Inversão Cromossômica , Genes de Imunoglobulinas , Cadeias kappa de Imunoglobulina/genética , Sequência de Bases , Deleção Cromossômica , Clonagem Molecular , Humanos , Dados de Sequência Molecular , Hibridização de Ácido Nucleico , Mapeamento por Restrição , Transcrição GênicaRESUMO
The recombination process that joins a VK to a JK segment of an immunoglobulin gene generates a second, reciprocal recombination product called f fragment. In this second product the regions flanking the VK and JK segments in the germline are joined in a head to head fashion. We now analysed f fragments in the human lymphoid cell lines Daudi, JI and IARC/BL41. All three f fragments contain JK1 flanks; the VK derived moiety of f Daudi and f41 could be traced back to known germline VK genes. There is a precise head to head joining of the heptanucleotide signal sequences in f Daudi and fJI while in f41 six nucleotides are present between the signal sequences. In contrast to the VK-JK recombination products, the f fragments were found to lack somatic mutations. The structures of the f fragments are discussed in the context of the VK-JK rearrangement mechanism.
Assuntos
DNA Recombinante/metabolismo , Genes , Cadeias Leves de Imunoglobulina/genética , Região Variável de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Alelos , Sequência de Bases , Linfoma de Burkitt , Linhagem Celular , Clonagem Molecular , Enzimas de Restrição do DNA , HumanosRESUMO
The linking of the human VK and JKCK gene regions (abbreviations in ref. 1) by chromosomal walking is reported. Hybridization experiments with the DNA of a somatic cell hybrid containing the region between JKCK and the telomer show that none of the major VK gene clusters is located downstream of CK. The distance between the VK and JK genes was found to be 23 kb. The JK proximal VK gene is the B3 gene which is the only representative of subgroup IV in the genome. This gene and the neighbouring B2 gene (accompanying paper) are arranged in opposite orientation to JKCK and can therefore rearrange only by an inversion mechanism. This finding is used, together with previous data, to delineate the rearrangement processes in the Burkitt lymphoma derived cell line BL21 as comprising an inversion in the first and a deletion in the second step.
Assuntos
Mapeamento Cromossômico , Regiões Constantes de Imunoglobulina/genética , Região de Junção de Imunoglobulinas/genética , Região Variável de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/genética , Mapeamento Cromossômico/métodos , Clonagem Molecular , Genes de Imunoglobulinas , Ligação Genética , Humanos , Hibridização de Ácido Nucleico , Recombinação GenéticaRESUMO
The question of how many V kappa gene segments exist in the human germ line was addressed. Seventy-five V kappa genes of the kappa locus and twenty-five V kappa genes localized outside of the locus ("orphons") had been cloned previously; 67 of the genes and 19 of the orphons had already been sequenced yielding 36 and 1 potentially functional V kappa genes, respectively, the remaining ones being pseudogenes. We now (a) determined the relative hybridization intensities of the cloned V kappa genes and orphons, (b) identified the bands in blot hybridizations of genomic DNA digests with the cloned genes and orphons, (c) determined the band intensities in the genomic DNA digests from two individuals and one cell line, (d) normalized the results with the help of the C kappa gene segment which is present in the haploid genome in one copy, (e) compared the genomic blot hybridization patterns with patterns of equimolar mixtures of the cloned V kappa genes and orphons, and (f) defined the bands and fractional intensities in bands that could not be assigned to cloned genes or orphons. From the resulting data we conclude that there are 5-7 still uncloned V kappa genes in germ-line DNA in addition to the 75 known V kappa genes and in addition to the 25 orphons 12-15 orphon candidates. It appears that the rheumatoid factor light chains of the Wa and 6B6.6 idiotypes are coded for by one V kappa III gene each. It is concluded that the kappa locus comprises no more than 50 potentially functional genes and no more than 85 V kappa genes altogether.