Search PubMed⌕ Search

Biomedical subjects

J W Gordon

Publications and source records attributed to J W Gordon.

At least 91 records · Page 5Linked to original sources
PubMed1988

Anemia in a line of transgenic mice carrying a mutant dihydrofolate reductase gene.

Several lines of transgenic mice were produced by pronuclear injection of a full-length cDNA encoding a mutant dihydrofolate reductase (DHFR, E.C. 1.5.1.3). The mutation causes altered enzyme kinetics for folate reduction as well as low affinity for methotrexate (MTX). One line of mice carrying the plasmid displays a moderate-to-severe anemia that is evident in fetuses and newborn mice and that moderates with age. RNA studies revealed high levels of transcription of the mutant gene in the fetal and adult liver, and low or absent expression in adult bone marrow. Transcription of the mutant gene was not found in the fetal liver of other pedigrees examined. The data thus suggest that expression of this mutant gene in the main hematopoietic organ of the fetus adversely affects erythropoiesis by altering the cellular environment for erythroid differentiation, and that translocation of the site of hematopoiesis to bone marrow, where the foreign gene is not expressed, leads to normalization of red cell production.

Anemia↗
PubMed1988

Cleavage characteristics of mouse embryos inseminated and cultured after zona pellucida drilling.

The effects of zona drilling on mouse embryo development in vitro were evaluated. Following insemination, sperm were immediately concentrated at the area of drilling, and in zona-drilled eggs, pronuclei appeared 30-50 min earlier than in zona-intact controls. Zona-drilled oocytes fertilized at significantly higher rates than undrilled controls and, consequently, a greater percentage of eggs inseminated after zona drilling reached the blastocyst stage. The attrition rates of zona-drilled embryos at each cleavage stage did not differ significantly from controls. Manipulated embryos exhibited unique cleavage patterns. Some embryos lost their zonae entirely, whereas others became partially extruded at early cleavage stages. These anomalies led to separation of blastomeres from the zygote proper, aggregation of embryos to form giant composite morulae and blastocysts, and occasionally to formation of miniature twin blastocysts. These characteristics of cleavage indicate that although zona drilling of a cohort of oocytes is likely to lead to an increased number of live births relative to controls, some developmental abnormalities can be encountered, and these may be associated with embryo loss, spontaneous chimerism, or possibly with conception of monozygotic twins.

Animals↗
PubMed1988

Fertilization of human oocytes by sperm from infertile males after zona pellucida drilling.

Infertile couples who had failed to achieve fertilization of oocytes in previous trials of in vitro fertilization (IVF) were treated by IVF with zona pellucida drilling. Zona drilling entails use of micromanipulation to introduce a gap in the zona pellucida either mechanically or by localized application of a zona solvent from a microneedle. Ten couples were treated, from whom 63 oocytes were recovered for manipulation. Sixteen eggs were denuded of the cumulus oophorus only, and the remaining 47 eggs were subjected to zona drilling. Of the 16 eggs denuded but not drilled, 4 (25%) were fertilized. Of the 47 oocytes drilled, 31 survived (67%) and 10 of the surviving eggs (32%) were fertilized. The polyspermy rate for drilled eggs that fertilized was high (5/10, 50%), and polyspermic eggs were often penetrated by more than two spermatozoa. The remaining five eggs fertilized after drilling were diploid fertilizations, and in three cases cleavage was followed by embryo transfer, although pregnancies were not obtained. These data indicate that zona drilling has the potential for establishing pregnancies in instances where treatment by standard IVF would fail. In addition, results indicate that the block to polyspermy in human eggs occurs at the level of the zona pellucida.

Female↗
PubMed1987

Regulation of Thy-1 gene expression in transgenic mice.

Genomic DNA fragments encompassing the human Thy-1 or mouse Thy-1.1 gene have been microinjected into pronuclei of mouse embryos homozygous for the Thy-1.2 allele. In the resulting transgenic mice, the human gene is expressed in a pattern characteristic of normal human tissues, and is not influenced by the pattern of endogenous mouse Thy-1 expression. The mouse Thy-1.1 gene fragment is expressed in a pattern typical of mouse Thy-1, although it is more limited in its distribution. The results indicate the presence of multiple cis-acting regulators of Thy-1 gene expression that have changed in both their character and arrangement over the course of Thy-1 gene evolution.

Animals↗
PubMed1987

Restriction enzyme evidence for Alu sequence-mediated dispersion of microinjected genes in transgenic mice.

A human bacteriophage clone containing adult beta-globin genes with four Alu sequences was microinjected to produce transgenic mice. Southern blot analysis on the spleen of a transgenic mouse revealed an unusual hybridization pattern that suggested extensive dispersion of human DNA throughout the mouse genome. This pattern was reproducible using several restriction enzymes, including a noncutting enzyme. The hybridization pattern was not observed in other tissues, and sequences were not detected in progeny using the bacteriophage probe. However, hybridization of spleen DNA of offspring against a human Alu probe revealed genetic transmission of human Alu sequences. The results suggest dispersion of microinjected Alu sequences throughout the genome.

Animals↗
PubMed1987

The perceptual attack time of musical tones.

Perceptual attack time (PAT) is defined as the time a tone's moment of attack or most salient metrical feature is perceived relative to its physical onset. Experiments are described that measured the PATs of recorded orchestral instrument tones by means of an interactive procedure with a computer and digital music synthesizer. Some PAT prediction models were then developed and tested against the empirical data. The most successful model had a correlation of 0.995 between measured and predicted PATs. The PAT is dependent on both rise time and listening level, indicating that the slope of the rise function is a key factor. Duration and spectrum can also act as cues to PAT, but are much less influential than amplitude or intensity cues. Possible relations to findings in physiology, particularly to the phenomenon of short-term adaptation in the firing of auditory fibers, are discussed.

Auditory Perception↗
PubMed1987

Ion pump ATPase inhibitors block the fertilization of zona-free mouse oocytes by acrosome-reacted spermatozoa.

The acrosome reaction was induced in nearly 100% of mouse spermatozoa with dibutyryl cyclic guanosine monophosphate (dbcGMP) before ouabain treatment. Acrosome-reacted spermatozoa could not penetrate the zona pellucida, but readily fertilized zona-free eggs. Exposure to ouabain at concentrations as low as 10(-7) M had a noticeable inhibitory effect upon fertilization. Similar results were obtained with a second ATPase inhibitor, digoxin. These results show that ion-pump inhibitors block the union of gametes which are otherwise fully competent to fertilize. These findings suggest that a membrane potential maintained by ion pumps is a necessary prerequisite for gamete fusion.

Acrosome↗
PubMed1986

Capacitated, acrosome reacted but immotile sperm, when microinjected under the mouse zona pellucida, will not fertilize the oocyte.

We have devised a procedure for mechanically inserting intact, acrosome reacted spermatozoa under the mouse zona pellucida, and have examined the ability of sperm so inserted to fertilize the mouse oocyte. Sperm immobilized by a variety of different methods are unable to fertilize the egg, despite the fact that electron microscopy confirms that they are acrosome reacted. Control experiments show that the oocytes are capable of being fertilized by motile sperm after the microinjection procedure, and that the immobilized sperm are able to form male pronuclei after injection directly into the ctyoplasm. These results indicate that in addition to its importance for penetration of egg investments, sperm motility is required for fusion of the gametes. Alternatively, the findings suggest that the enzymatic machinery required for sperm motility is very similar to that utilized for gamete fusion, and that destruction of one is likely to lead to inactivation of the other.

Acrosome↗
PubMed1986

Assisted fertilization by zona drilling: a mouse model for correction of oligospermia.

A micromanipulation apparatus was used to produce holes in the zonae pellucidae of unfertilized mouse oocytes. A microneedle loaded with acid Tyrode's solution was brought into contact with the zona surface, and positive flow was used in conjunction with mechanical pressure to cause a localized dissolution of the zona. Treated eggs were then fertilized in vitro in comparison with control cells. The zona drilling procedure decreased the sperm count required to achieve fertilization by a factor of approximately 100. The rate of polyspermy in zona-drilled oocytes was not greater than in controls, and oocytes fertilized after drilling, when implanted into pseudopregnant foster females, developed to term at the same rate as controls. The results demonstrate that zona drilling is a safe, effective method of increasing the efficiency of fertilization in vitro and may be useful both in agriculture and medicine for conferring fertility upon males with low sperm counts.

Animals↗
PubMed1986

Systemic resistance to methotrexate in transgenic mice carrying a mutant dihydrofolate reductase gene.

A full-length cDNA coding for a mutant dihydrofolate reductase (DHFR; 5,6,7,8-tetrahydrofolate: NADP+ oxidoreductase, EC 1.5.1.3), cloned from a mouse fibroblast cell line grown in high concentrations of methotrexate (MTX), was microinjected into mouse embryos to produce transgenic mice. The DHFR cDNA product is 270-fold more resistant to MTX than the wild-type enzyme. Seventeen transgenic mouse lines, identified by Southern blotting of tail or spleen DNA, carried between 1 and 400 copies of the foreign gene per cell. Eight lines have thus far been tested for resistance to MTX. Control mice were treated until death; MTX was withdrawn from transgenic mice when a cumulative MTX dose uniformly fatal for controls was reached. The major site of MTX toxicity was the gastrointestinal tract, with death of controls resulting from fluid and weight loss. Transgenic animals were relatively resistant to these symptoms and tolerated significantly more MTX than control animals. These results show that genes conferring resistance to chemotherapeutic agents can, after transfer into intact organisms, produce systemic drug resistance.

Animals↗
PubMed1986

A foreign dihydrofolate reductase gene in transgenic mice acts as a dominant mutation.

We have produced 17 lines of transgenic mice by microinjecting a full-length cDNA clone of an altered dihydrofolate reductase (dhfr) gene. The protein specified by this gene carries a point mutation which triples its Km for dihydrofolate and reduces substrate turnover 20-fold relative to the wild-type enzyme. Transgenic mice from different pedigrees, several of which carry a single copy of this gene in different integration sites, manifest an array of similar developmental abnormalities including growth stunting, reduced fertility, pigmentation changes, and skeletal defects. These defects appear in animals heterozygous for the foreign gene. RNA analyses demonstrate significant expression of the cDNA in newborn mice and adult tissues. These findings show that the additional dhfr gene exerts its mutational effects in a dominant fashion, and therefore the data indicate that transgenic mice can serve as models for elucidating mechanisms of dominant mutagenesis.

Animals↗
PubMed1985

DNA-mediated genetic transformation of mouse embryos and bone marrow--a review.

In recent years, new gene transfer systems have been developed which allow molecularly cloned genetic material to be introduced into whole organisms. These systems include the microinjection of DNA into mammalian embryos, transfection of DNA into mouse bone marrow cells, and the infection of early embryos with retroviruses. Exogenous DNA appears to integrate randomly into the host genome. The production of transgenic mice by injection of DNA into mouse embryos has rapidly gained importance as an experimental tool for the study of gene regulation during development. Through this technique, recombinant molecules of any type can be introduced into one-celled embryos, and thus can be used to study development from its earliest stages. DNA sequences have been shown to integrate and transmit through the germ line to subsequent generations as mendelian traits. Transgenic mice carrying various gene constructs have been successfully exploited for the elucidation of factors which determine tissue specificity of gene expression as well as the level of gene control. Phenotypic changes related to expression of foreign genes have also been observed. This experimental approach thus promises to rapidly solve many of the heretofore most challenging problems in developmental genetics. Insertion of foreign genes has also made possible the creation of insertional mutants which manifest themselves most frequently as recessives. Such mutations can be readily studied at the molecular level by using the transferred material as a probe for recovery of the affected host sequence from genomic libraries. Many of these same problems have been addressed by introducing retroviral DNA into mouse embryos. Here, the sequences used for transfer have been limited to retroviral genes, but nonetheless these experiments have been profitably exploited for studies both of gene regulation and mutagenesis. Gene transfer systems are being developed allowing the experimenter to transfer DNA into bone marrow cells of mice, after which the recipient cells can be reintroduced into lethally irradiated histocompatible animals. This system has the advantage that selection can be applied during the gene transfer process such that the expression of the foreign material is assured. In addition, these experiments have created a model system for production of animals carrying a subpopulation of cells which is highly resistant to a toxic agent. This system has the potential for therapeutic application to man.

Animals↗
PubMed1983

Studies of foreign genes transmitted through the germ lines of transgenic mice.

A novel gene transfer system has recently been developed in which DNA sequences isolated by molecular cloning can be introduced and permanently integrated into the genomes of developing mice. The procedure entails the microinjection of such cloned sequences into the pronuclei of one-celled embryos followed by reimplantation into pseudopregnant females for continued development. Although data obtained from this system are still few, they indicate it will have broad applicability to problems of mammalian developmental genetics. In order that such experiments be fully exploited, it will be necessary to understand the behavior of foreign genes introduced into the mouse and the relationship of that behavior to endogenous gene structure, function, and regulation. As a step in this direction, we have examined a line of mice into which has been transferred a recombinant plasmid consisting of a human leukocyte interferon genomic fragment cloned into the BamHI site of pBR322. The donor material has been integrated as a large concatameric structure which is inherited as a single Mendelian trait to several generations of progeny. Crossing of heterozygotes has apparently resulted in the production of viable homozygotes. In one animal, the structure of the integrated fragment was altered in spleen DNA but not in germ cells. This finding may reflect a normal processing mechanism whereby the structure of genes is altered during cell differentiation, or it may mean that transferred DNA does not behave as endogenous genes do.

Animals↗
PubMed1982

Germ line transmission in transgenic mice.

Our laboratory has recently demonstrated the successful transfer of genetic material into the genomes of newborn mice by injection of that material into pronuclei of fertilized eggs. Our initial results indicated two patterns of processing of the injected DNA: one in which the material was not integrated into the host genome, and another in which the injected genes became associated with high molecular weight DNA. We now present evidence that these patterns are maintained through further development to adulthood. We provide definitive evidence of the covalent association of injected DNA with host sequences, and transmission of such linked sequences in a Mendelian distribution to 2 succeeding generations of progeny. The observation that injected gene sequences can become integrated and stably transmitted through the germ line should contribute significantly to further studies of this gene transfer system.

Aging↗