RESUMEN
The H-2Dd transgenic strain D8 on C57BL background was more resistant to subcutaneous challenge of RBL-5 lymphoma cells than B6 controls. The direct role of the H-2Dd antigen was investigated by the use of (D8 x B6)F1 crosses and (D8 B6) x B6 backcrosses. The latter showed cosegregation with regard to Dd antigen expression and lymphoma resistance, both of which were inherited in a pattern consistent with control by a single dominant gene. The rejection potential in (D8 x B6)F1 mice appeared as strong as that seen in crosses between B6 and MHC congenic mice (on B10 background) carrying H-2Dd. The lymphoma resistance could be abrogated by treatment with anti-asialo GM1 antiserum or anti-NK 1.1 mAb, indicating a role for NK cells.
Asunto(s)
Antígenos H-2/genética , Linfoma/inmunología , Animales , Regulación de la Expresión Génica , Antígeno de Histocompatibilidad H-2D , Células Asesinas Naturales/inmunología , Complejo Mayor de Histocompatibilidad , Ratones , Ratones Endogámicos C57BL , Ratones Transgénicos , Trasplante de NeoplasiasRESUMEN
DNA-mediated gene transfer is a procedure which uses purified DNA to introduce new genetic elements into cells in culture. The standard DNA-mediated gene transfer procedure involves the use of whole cell DNA as carrier DNA for the transfer. We have modified the standard DNA-mediated gene transfer procedure to transfer the Herpes simplex virus type 1 thymidine kinase gene (TK) into TK- murine recipient cells in the absence of whole cell carrier DNA. The majority (8/10) of carrier-free transformant lines expressed the TK+ phenotype stably, in sharp contrast to our results with carrier-containing DNA-mediated gene transfer. There was a wide range in donor DNA content among independent transformants. Further analysis on one transformant line using DNA restriction digests and in situ hybridization provided evidence that, in the absence of whole cell carrier DNA, multiple donor DNA sequences became integrated at a single chromosomal site.
Asunto(s)
ADN/genética , Transformación Genética , Animales , Línea Celular , ADN Circular , Regulación de la Expresión Génica , Vectores Genéticos , Ratones , Plásmidos , Recombinación Genética , Simplexvirus/genética , Timidina Quinasa/genéticaRESUMEN
Two plasmids containing nonoverlapping deletions of the herpes simplex virus thymidine kinase gene were introduced into thymidine kinase-deficient mouse L cells by DNA-mediated gene transfer. Thymidine kinase-producing transformants were generated by a mixture of the two plasmids at a frequency significantly greater than that generated by either plasmid alone. Southern blot analyses demonstrated that functional thymidine kinase genes were generated by homologous recombination between the two deletion mutants.
Asunto(s)
Ingeniería Genética , Plásmidos , Recombinación Genética , Timidina Quinasa/genética , Animales , Secuencia de Bases , Células Cultivadas , Deleción Cromosómica , Ratones , Mutación , SimplexvirusRESUMEN
Rejection of bone marrow grafts in irradiated mice is mediated by natural killer (NK) cells and is controlled by genes linked to the major histocompatibility complex (MHC). It has, however, not been possible to identify the genes or their products. An MHC class I (Dd) transgene introduced in C57BL donors prevented the rejection of their bone marrow by NK cells in irradiated allogeneic and F1 hybrid mice expressing the Dd gene. Conversely, H-2Dd transgenic C57BL recipients acquired the ability to reject bone marrow from C57BL donors but not from H-2Dd transgenic C57BL donors. These results provide formal evidence that NK cells are part of a system capable of rejecting cells because they lack normal genes of the host type, in contrast to T cells, which recognize cells that contain abnormal or novel sequences of non-host type.
Asunto(s)
Trasplante de Médula Ósea , Genes MHC Clase I , Rechazo de Injerto , Antígenos H-2/genética , Animales , Células Asesinas Naturales/inmunología , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Ratones Transgénicos , Trasplante HomólogoRESUMEN
Alzheimer's disease is characterized by widespread deposition of amyloid in the central nervous system. The 4-kilodalton amyloid beta protein is derived from a larger amyloid precursor protein and forms amyloid deposits in the brain by an unknown pathological mechanism. Except for aged nonhuman primates, there is no animal model for Alzheimer's disease. Transgenic mice expressing amyloid beta protein in the brain could provide such a model. To investigate this possibility, the 4-kilodalton human amyloid beta protein was expressed under the control of the promoter of the human amyloid precursor protein in two lines of transgenic mice. Amyloid beta protein accumulated in the dendrites of some but not all hippocampal neurons in 1-year-old transgenic mice. Aggregates of the amyloid beta protein formed amyloid-like fibrils that are similar in appearance to those in the brains of patients with Alzheimer's disease.
Asunto(s)
Enfermedad de Alzheimer/genética , Péptidos beta-Amiloides/genética , Encéfalo/metabolismo , Enfermedad de Alzheimer/patología , Péptidos beta-Amiloides/análisis , Animales , Secuencia de Bases , Encéfalo/patología , ADN/genética , Hipocampo/ultraestructura , Humanos , Ratones , Ratones Transgénicos , Microscopía Electrónica , Datos de Secuencia Molecular , Neurofibrillas/ultraestructura , Sondas de Oligonucleótidos , Mapeo RestrictivoRESUMEN
Cell line 101 is a thymidine kinase (TK)-positive derivative of Ltk- which contains ca. 20 copies of the herpes simplex virus TK gene organized in a tandem array. DNA methylation at three sites within the gene and flanking sequences was inversely correlated with expression: the sites were unmethylated in line 101, methylated in each of 4 TK-negative derivatives of 101, and unmethylated in each of 21 TK-positive derivatives derived from them. The same three sites were affected in most of the 20 copies of the TK gene, whereas other sites between them were not affected. Although the entire gene cluster was never lost, indicating that integration into the genome was stable, internal rearrangements occurred at a high frequency. The rearrangements had no obvious correlation with the state of methylation or with the expression of the genes.
Asunto(s)
Regulación de la Expresión Génica , Metilación , Timidina Quinasa/genética , Animales , Genes , Ligamiento Genético , Ratones , Recombinación GenéticaRESUMEN
Bovine papillomavirus (BPV) was methylated in vitro at either the 29 HpaII sites, the 27 HhaI sites, or both. Methylation of the HpaII sites reduced transformation by the virus two- to sixfold, while methylation at HhaI sites increased transformation two- to fourfold. DNA methylated at both HpaII and HhaI sites did not differ detectably from unmethylated DNA in its efficiency of transformation. These results indicate that specific methylation sites, rather than the absolute level of methylated cytosine residues, are important in determining the effects on transformation and that the negative effects of methylation at some sites can be compensated for by methylation at other sites. BPV molecules in cells transformed by methylated BPV DNA contained little or no methylation, indicating that the pattern of methylation was not faithfully retained in these extrachromosomally replicating molecules. Methylation at the HpaII sites (but not the HhaI sites) in the cloned BPV plasmid or in pBR322 also inhibited transformation of the plasmids into Escherichia coli HB101 cells.
Asunto(s)
Papillomavirus Bovino 1/patogenicidad , Transformación Celular Viral , Desoxirribonucleasas de Localización Especificada Tipo II , Papillomaviridae/patogenicidad , Animales , Secuencia de Bases , Clonación Molecular , ADN (Citosina-5-)-Metiltransferasas/metabolismo , Enzimas de Restricción del ADN/metabolismo , ADN Viral/metabolismo , Desoxirribonucleasa HpaII , Escherichia coli/genética , Metilación , RatonesRESUMEN
The major histocompatibility complex class I genes play an essential role in the immune presentation of aberrant cells. To gain further insight into the regulation of the expression of these class I genes and to better define the functions of their protein products, we made use of the technique of gene transfer into the germ line of inbred mice. With the use of locus-specific DNA probes, we observed that a transgenic class I gene was expressed in a tissue-dependent fashion analogous to that of an endogenous class I gene. In addition, the level of expression of the transgenic gene was substantially higher that that of the endogenous gene. The availability of transgenic mice properly expressing a foreign murine class I gene provides a unique system to further define the role of the class I antigens in the maturation of the immune response and in determining the malignant and metastatic phenotypes of tumor cells.
Asunto(s)
Genes Reguladores , Antígenos H-2/genética , Complejo Mayor de Histocompatibilidad , Animales , Secuencia de Bases , ADN/metabolismo , Genes , Antígenos HLA-D/análisis , Haplotipos , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BLRESUMEN
The regulated expression of major histocompatibility complex class I antigens is essential for assuring proper cellular immune responses. To study H-2 class I gene regulation, we have transferred a foreign class I gene to inbred mice and have previously shown that the heterologous class I gene was expressed in a tissue-dependent manner. In this report, we demonstrate that these mice expressed the transgenic class I molecule on the cell surface without any alteration in the level of endogenous H-2 class I antigens. Skin grafts from transgenic mice were rapidly rejected by mice of the background strain, indicating that the transgenic antigen was expressed in an immunologically functional form. As with endogenous H-2 class I genes, the class I transgene was inducible by interferon treatment and suppressible by human adenovirus 12 transformation. Linkage analysis indicated that the transgene was not closely linked to endogenous class I loci, suggesting that trans-regulation of class I genes can occur for class I genes located outside the major histocompatibility complex.
Asunto(s)
Genes , Antígenos HLA/genética , Complejo Mayor de Histocompatibilidad , Transcripción Genética , Animales , Línea Celular , Células Cultivadas , Regulación de la Expresión Génica , Rechazo de Injerto , Ratones , Ratones Endogámicos , Ratones Transgénicos , ARN Mensajero/genética , Trasplante de Piel , Especificidad de la Especie , Trasplante HomólogoRESUMEN
Two plasmids, one containing the simian virus 40 (SV40) genome and the mouse metallothionein I gene and one containing the v-myc gene of avian myelocytomatosis virus MC29, were coinjected into mouse embryos. Of the 13 surviving mice, one, designated M13, contained both myc and SV40 sequences. This mouse developed a cranial bulge identified as a choroid plexus papilloma at 13 weeks and was subsequently sacrificed; tissue samples were taken for further analysis. Primary cell lines derived from these tissues contained both myc and SV40 DNA. No v-myc mRNA could be detected, although SV40 mRNA was present in all of the cell lines tested. T antigen also was expressed in all of the cell lines analyzed. These data suggest that SV40 expression was involved in the abnormalities of mouse M13 and was responsible for the transformed phenotype of the primary cell lines. Primary cell lines from this mouse were atypical in that the population rapidly became progressively more transformed with time in culture based on the following criteria: morphology, growth rate, and the ability to grow in soft agar and in serum-free medium. The data also suggest that factors present in the mouse regulated the ability of SV40 to oncogenically transform most cells and that in vitro culture of cells allowed them to escape those factors.
Asunto(s)
Neoplasias del Ventrículo Cerebral/genética , Ratones/genética , Oncogenes , Papiloma/genética , Virus 40 de los Simios/genética , Animales , Plexo Coroideo , Metilación , ARN Viral/análisis , Distribución TisularRESUMEN
To elucidate mechanisms involved in deoxyribonucleic acid-mediated gene transfer, we transferred the herpes simplex virus thymidine kinase gene (TK) into mouse Ltk- cells. Independent TK+ clones (transformants) and derivatives of each were tested for phenotypic expression and the presence and arrangement of TK sequences. Initially, transformants expressed viral TK unstable, with 10% of the cells in each generation losing both the TK+ phenotype and virally derived TK sequences. After a prolonged period in culture, stable subpopulations arose from which the TK+ phenotype and viral sequences were no longer lost at detectable frequency. Analysis of unstable cell populations indicated that individual viral deoxyribonucleic acid molecules were reduced in size, but were linked to other deoxyribonucleic acid to form molecules large enough to be precipitated in a Hirt fractionation. We term these molecules transgenomes. Analysis of independent unstable subclones derived from the primary transformants demonstrated that individual transgenomes could contain multiple copies of the viral TK sequences. Recipient cell lines frequently possessed more than one type of transgenome and possibly multiple copies per cell of each type. Stable derivatives possessed only one of the transgenomes present in the unstable parent, and these sequences were associated with a recipient cell chromosome.
Asunto(s)
ADN/genética , Transfección , Animales , Línea Celular , Clonación Molecular , Genes Virales , Ratones , Fenotipo , Plásmidos , Simplexvirus/enzimología , Simplexvirus/genética , Timidina Quinasa/genéticaRESUMEN
The ability of mammalian cells to take up exogenously added DNA and to express genes included on that DNA has been well documented. DNA-mediated gene transfer (DMGT) potentially is a useful technique for the elucidation of many of the factors that control gene expression, and for the purification and isolation of mammalian genes. Before many of the benefits can be realized, however, a more detailed understanding of the organization, intracellular location, and expression of transferred genes will be needed. Recent studies have begun to characterize the DMGT process. Selected genes become linked to other exogenously added DNA during or subsequent to transfer and persist in the nuclei of recipient cells as part of large molecules called transgenomes. Transgenomes initially are maintained unstably and are lost from the population with first order kinetics. After a variable number of generations in culture, subpopulations arise that maintain the transferred genes stably. In these "stable" cells the transgenome is associated with a recipient cell chromosome, although the particular chromosome differs in independent "stable" lines. Mixture of an excess of specific nonselectable genes with the selected gene prior to transfer results in the inclusion of the nonselected genes in the transgenomes present in most cells that survive selection. This finding demonstrates the feasibility of introducing virtually any purified gene into mammalian cells. Recently microinjection of DNA directly into the nuclei of cells has been demonstrated. This technique greatly increases the frequency of gene transfer and significantly expands the number of cell types that can be genetically transformed.
Asunto(s)
ADN/genética , Regulación de la Expresión Génica , Transformación Genética , Animales , Línea Celular , Cromosomas/fisiología , ADN Recombinante , Hipoxantina Fosforribosiltransferasa/genética , Mamíferos/genética , Timidina Quinasa/genéticaRESUMEN
Plasmid pTKx-1, containing the herpes simplex virus gene for thymidine kinase (TK) inserted into the BamHI site of plasmid pBR322, was introduced into Ltk- cells by calcium phosphate precipitation in the absence of carrier DNA. Line 101 is a TK+ derivative of Ltk- that contains multiple copies of pTKx-1 in a multimeric structure. A derivative of 101 that retained but no longer expressed the herpes simplex TK genes (termed 101BU1) and derivatives of line 101BU1 that reexpressed the genes (termed 101H1, 101HC, and 101HG) were selected. The TK genes in 101BU1 were hypermethylated relative to those in the TK+ parent and derivatives. Growth of 101BU1 in the presence of the methylation inhibitor 5-azacytidine resulted in an average 13-fold increase in the number of TK+ reexpressors, DNA from 101BU1 was inactive in secondary gene transfer, whereas DNA from 101 and from TK+ reexpressors was active. These data support a causative relationship between DNA methylation and decreased gene expression. All TK+ reexpressors examined had DNA rearrangements involving TK DNA.
Asunto(s)
Regulación de la Expresión Génica , Timidina Quinasa/genética , Animales , Azacitidina/farmacología , Regulación de la Expresión Génica/efectos de los fármacos , Genes , Genes Virales , Ligamiento Genético , Células L , Metilación , Ratones , Simplexvirus/genéticaRESUMEN
We have described the development of a selective system useful for the identification and characterization of onc genes capable of conferring growth factor independence. The use of defined, serum-free media allows us to select for transformed cells which have lost specific growth factor requirements. We have used this system to show that several cloned onc genes generate different transformed phenotypes with respect to growth factor requirements. BPV-1 is active in relieving contact inhibition, yet these transformed NIH/3T3 cells retain their stringent requirement for FGF. In contrast, sis and H-ras were equally proficient at relieving contact inhibition and the requirement for FGF. Sis induced equal numbers of colonies regardless of the presence or absence of insulin, however, H-ras-mediated colony formation decreased four-fold when insulin was removed. This suggests that H-ras is less efficient in relieving the insulin requirement than is sis. To determine if colony formation by H-ras is a function of dosage, we are conducting experiments to measure the level of expression of p21 in transformants selected with and without insulin in the media. We have also presented data to show that loss of contact inhibition and loss of growth factor requirements are dissociable phenotypes under separate control in some cells. Thus, it should be possible to use this selective system to identify transforming genes in tumor DNA. Since some of these genes may be undetectable by the standard focus forming assay, selection in MSF medium may prove to be a useful tool for identifying and elucidating the action of activated cellular onc genes.
Asunto(s)
Medios de Cultivo/metabolismo , Sustancias de Crecimiento/metabolismo , Oncogenes , Animales , División Celular , Línea Celular , Genes Virales , Sustancias de Crecimiento/genética , Humanos , Plásmidos , TransfecciónRESUMEN
In Escherichia coli C, the catabolism of the pentitols ribitol and D-arabitol proceeds through separate, inducible operons, each consisting of a dehydrogenase and a kinase. The ribitol operon is induced in response to ribulose, and the D-arabitol operon is induced in response to D-arabitol. Each operon is under negative control. The genes of the ribitol and D-arabitol operons are very closely linked and lie in a mirror image arrangement, rtlB-rtlA-rtlC-atlC-atlA-atlB, between metG and his on the E. coli chromosome.
Asunto(s)
Escherichia coli/metabolismo , Operón , Ribitol/metabolismo , Alcoholes del Azúcar/metabolismo , Mapeo Cromosómico , Cromosomas Bacterianos , Escherichia coli/enzimología , Escherichia coli/genética , Prueba de Complementación Genética , Ligamiento Genético , Oxidorreductasas/metabolismoRESUMEN
Ribitol+ strains of Escherichia coli acquire the ability to utilize xylitol by mutating to constitutive production of the coordinately controlled ribitol catabolic enzymes ribitol dehydrogenase (RDH) and D-ribulokinase (DRK). Such strains concomitantly acquire toxicity to galacitol and L-arabitol, and to D-arabitol if they are unable to utilize it for growth. Strains selected for resistance to these polyols have DRK structural gene mutations or other mutations that eliminate the constitutive production of DRK, consistent with the view that DRK phosphorylates those polyols to toxic substances. Ribitol+ strains selected for growth on 8 mM xylitol fail to grow on 30 mM xylitol. A product of ribitol and xylitol catabolism represses synthesis of RDH, an enzyme required for growth on xylitol. At 30 mM xylitol, greater than 99% of RDH synthesis is repressed. Strains that grow on 8 mM xylitol can mutate to grow on 30 mM xylitol. Such mutants, relieved of this repression, overproduce RDH, resulting in good growth on the poor substrate, xylitol, but poor growth on the normal substrate, ribitol.
Asunto(s)
Escherichia coli/metabolismo , Genes , Xilitol/metabolismo , Escherichia coli/genética , Operón , Oxidorreductasas/biosíntesis , Fosfotransferasas/biosíntesis , Ribitol/metabolismo , Alcoholes del Azúcar/metabolismoRESUMEN
All of our Escherichia coli C mutants blocked in the first step of D-arabitol catabolism (D-arabitol dehydrogenase) became unable to grow in the presence of D-arabitol. We have shown that this sensitivity is eliminated by a defect in the second enzyme of the pathway (D-xylulokinase), leading to a pattern of toxicity and its relief which has not been previously reported. We have found a similar pattern of toxicity and its relief in the closely related ribitol pathway. The evolutionary significance of these findings is discussed.