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J D Gross

Publications and source records attributed to J D Gross.

At least 19 recordsLinked to original sources

Identification of the cell fate gene stalky in Dictyostelium.

Using insertional mutagenesis, we have isolated a "stalky" mutant in which cells destined to become spores end up as stalk cells. Similar mutants were previously observed after chemical mutagenesis, but the affected gene could not be isolated. Our mutant, like the previous ones, is in stkA. Its defect is cell-autonomous and not overcome by overexpressing cAMP-dependent protein kinase. stkA is strongly expressed in the prespore region of aggregates but not in the anterior prestalk zone. The mutant expresses normal levels of prespore-cell transcripts but fails to produce the spore transcript spiA. stkA encodes a predicted 99 kDa protein (STKA) with two putative C4 zinc fingers, one of which is a GATA-type finger, indicating that it may be a transcription factor. This conclusion is supported by localization of STKA in the nucleus.

Amino Acid Sequence

Vacuolar H(+)-ATPase and weak base action in Dictyostelium.

Amoebae of Dictyostelium discoideum release ammonia during development, and the accumulation of this weak base is believed to be responsible for inhibiting fruiting-body formation and switching aggregates into migrating slugs. Exposure to weak bases can also inhibit aggregation and cell-type specific gene expression. The pathway by which weak bases influence development is not understood. We show here that the development of a set of mutants defective in acidification of intracellular acidic compartments is abnormally sensitive to inhibition by weak bases. Moreover even in the absence of added weak bases these mutants are delayed in aggregation and have a protracted migratory phase. The same behaviour is observed in transformants harbouring an antisense construct for one of the vacuolar H(+)-ATPase subunits. These results support the idea that weak bases exert their effects by inhibiting acidification of an intracellular acidic compartment.

Acids

The role of calcium in aggregation and development of Dictyostelium.

Changes in cytosolic Ca2+ play an important role in a wide array of cell types and the control of its concentration depends upon the interplay of many cellular constituents. Resting cells maintain cytosolic calcium ([Ca2+]i) at a low level in the face of steep gradients of extracellular and sequestered Ca2+. Many different signals can provoke the opening of calcium channels in the plasma membrane or in intracellular compartments and cause rapid influx of Ca2+ into the cytosol and elevation of [Ca2+]i. After such stimulation Ca2+ ATPases located in the plasma membrane and in the membranes of intracellular stores rapidly return [Ca2+]i to its basal level. Such responses to elevation of [Ca2+]i are a part of an important signal transduction mechanism that uses calcium (often via the binding protein calmodulin) to mediate a variety of cellular actions responsive to outside influences.

Animals

Trapping developmental promoters in Dictyostelium.

Recently an insertional mutagenesis procedure has been developed to permit cloning of genes affected in developmental mutants of Dictyostelium discoideum (Kuspa and Loomis, Proc. Natl. Acad. Sci. USA 89, 8803-8807, 1992). In this procedure a plasmid bearing the URA (pyr5-6) gene is linearized with a restriction enzyme and electroporated into URA- amoebae (auxotrophic for uracil) together with the corresponding restriction enzyme. Transformants that can grow without uracil are screened for developmental defects resulting from insertion of the plasmid into a gene of developmental importance. We have modified this procedure to permit characterization of the promoters and structural sequences of genes that would be missed by the standard procedure because their disruption produces no obvious phenotype. Constructs carrying a promoter-less Escherichia coli lacZ gene were designed so that expression of lacZ requires insertion into an active host transcription unit. By screening restriction enzyme-generated transformants we have isolated several strains in which lacZ is under the control of a developmentally activated promoter and have cloned the 5' flanking DNA adjacent to the insertion site. Sequencing the junction between plasmid and host genome has confirmed in-frame fusion with the lacZ gene, and reintroduction of the cloned plasmids into parental cells has shown that the cloned sequences do actually contain the relevant promoters. This procedure should give ready access to a wide range of developmental promoters without the need for prior identification of the developmental genes involved.

Animals

Anion effects on vesicle acidification in Dictyostelium.

Chloride ions stimulated the ATP-dependent formation of a proton gradient in vesicles derived from amoebae of the cellular slime mould, D. discoideum, and reduced the formation of a membrane potential, inhibited rather than stimulated the formation of the proton gradient. Since bicarbonate ions did not inhibit H(+)-ATPase activity we conclude that they enter the vesicles and combine with translocated protons. This finding is consistent with the suggestion that the membranes of the light vesicle fraction are fragments of contractile vacuole complexes, and that these organelles increase their osmotic activity by taking up bicarbonate ions and protons from the cytoplasm, and then release water and carbonic acid into the extracellular milieu.

4-Chloro-7-nitrobenzofurazan

Characterisation of an intracellular Ca2+ pump in Dictyostelium.

Calcium uptake by microsomal membranes from the cellular slime mould Dictyostelium discoideum was measured using Calcium Green-2 as a fluorescent probe of external free Ca2+ concentration. High-affinity Ca2+ uptake was found to be completely inhibited by low concentrations of vanadate, but not by thapsigargin, suggesting that the activity is mediated by a Ca(2+)-ATPase distinct from sarco(endo)plasmic reticulum type of higher animal cells. On sucrose density gradients, Ca2+ uptake distributes with vacuolar proton pump activity and part of the observed Ca2+ uptake is dependent on the pH gradient generated by the vacuolar-type H(+)-ATPase, indicating that the Ca2+ pump is located on both acidic and non-acidic vesicles, possibly derived from the H(+)-ATPase-rich contractile vacuole complex.

Animals

Motion aftereffects with random-dot chequerboard kinematograms: relation between psychophysical and VEP measures.

A random-dot chequerboard kinematogram was used to investigate the effect of motion adaptation both on evoked potentials and on motion aftereffects (MAEs). The experimental paradigm used allowed simultaneous measurement of both variables. Each adaptation period was followed by a series of 5 short test stimuli to which evoked potentials were recorded. Motion aftereffects were observed in the intervals between test stimuli. An inverse relationship between mean N2-P1 amplitude and mean reported MAEs was found as a function of adaptation durations of 1.4, 5.6, and 17.5 s. When the shortest and longest adaptation durations were compared, this relationship held for thirteen of fourteen subjects tested when adaptation-motion and test-motion directions corresponded and for twelve of fourteen subjects when they were opposed. The possibility that the effect of motion adaptation on N2-P1 amplitude was due to local luminance-contrast adaptation is discussed and shown to be unlikely. The suitability of this paradigm for the combined psychophysical and electrophysiological assessment of disturbances in motion perception is discussed.

Adolescent

Developmental decisions in Dictyostelium discoideum.

A few hours after the onset of starvation, amoebae of Dictyostelium discoideum start to form multicellular aggregates by chemotaxis to centers that emit periodic cyclic AMP signals. There are two major developmental decisions: first, the aggregates either construct fruiting bodies directly, in a process known as culmination, or they migrate for a period as "slugs." Second, the amoebae differentiate into either prestalk or prespore cells. These are at first randomly distributed within aggregates and then sort out from each other to form polarized structures with the prestalk cells at the apex, before eventually maturing into the stalk cells and spores of fruiting bodies. Developmental gene expression seems to be driven primarily by cyclic AMP signaling between cells, and this review summarizes what is known of the cyclic AMP-based signaling mechanism and of the signal transduction pathways leading from cell surface cyclic AMP receptors to gene expression. Current understanding of the factors controlling the two major developmental choices is emphasized. The weak base ammonia appears to play a key role in preventing culmination by inhibiting activation of cyclic AMP-dependent protein kinase, whereas the prestalk cell-inducing factor DIF-1 is central to the choice of cell differentiation pathway. The mode of action of DIF-1 and of ammonia in the developmental choices is discussed.

Ammonia

Programmed cell death in Dictyostelium.

Programmed cell death (PCD) of Dictyostelium discoideum cells was triggered precisely and studied quantitatively in an in vitro system involving differentiation without morphogenesis. In temporal succession after the triggering of differentiation, PCD included first an irreversible step leading to the inability to regrow at 8 hours. At 12 hours, massive vacuolisation was best evidenced by confocal microscopy, and prominent cytoplasmic condensation and focal chromatin condensation could be observed by electron microscopy. Membrane permeabilization occurred only very late (at 40-60 hours) as judged by propidium iodide staining. No early DNA fragmentation could be detected by standard or pulsed field gel electrophoresis. These traits exhibit some similarity to those of previously described non-apoptotic and apoptotic PCD, suggesting the hypothesis of a single core molecular mechanism of PCD emerging in evolution before the postulated multiple emergences of multicellularity. A single core mechanism would underly phenotypic variations of PCD resulting in various cells from differences in enzymatic equipment and mechanical constraints. A prediction is that some of the molecules involved in the core PCD mechanism of even phylogenetically very distant organisms, e.g. Dictyostelium and vertebrates, should be related.

Animals

Ammonia hypersensitivity of slugger mutants of D. discoideum.

The weak base ammonia inhibits aggregation and culmination of wild-type amoebae of Dictyostelium discoideum. Here we have examined its effect on a series of 'slugger' mutants previously assigned to 10 complementation groups, and so-called because they remain as slugs for extended periods. We show that the mutants accumulate normal levels of ammonia and hence may be abnormally susceptible to the ammonia they produce. In agreement with this we find that representatives of the slugger complementation groups are hypersensitive to ammonia inhibition at three clearly recognisable morphological stages of development: aggregation, tip formation and culmination. This finding suggests that a common ammonia-sensitive process underlies each of these developmental events.

Amines

Magnetic resonance imaging evidence of a focal pontine ischemia in sudden hearing loss and seventh nerve paralysis.

Sudden sensorineural hearing loss (SSHL) has been associated with many etiologies. However, determining the exact cause of SSHL remains elusive. Recent reports have demonstrated the usefulness of magnetic resonance imaging in identifying the site of lesion in SSHL. This report presents the case of a 68-year-old male who presented with right-sided SSHL associated with right-sided facial paralysis. Magnetic resonance imaging demonstrated a focal area of increased signal on T2-weighted image within the right inferior pons, suggestive of a postischemic edematous focus. Magnetic resonance imaging is becoming important in establishing the etiology of SSHL. Magnetic resonance imaging findings in cases of hearing loss are discussed.

Aged

The target of ammonia action in dictyostelium.

The weak base ammonia is implicated in a number of key processes in Dictyostelium development, notably aggregation and culmination. To determine its intracellular site of action, we compared its biological potency with that of other weak bases. All the bases inhibited these developmental processes effectively, but differed manyfold in potency in accordance with their activity in dissipating pH gradients, as measured by in vivo 31P NMR with pH-sensitive phosphonate probes. These results indicate that weak bases influence development by raising the pH of an intracellular acidic compartment.

Alkalies

ATP-driven Ca2+/H+ antiport in acid vesicles from Dictyostelium.

Amoebae of the cellular slime mold Dictyostelium discoideum possess an extensive and dynamic endomembrane system that includes many types of acidic vacuoles. A light membrane fraction from Dictyostelium, rich in vacuolar-type H(+)-ATPase, has been described [Padh, H., Lavasa, M. & Steck, T.L. (1989) J. Cell Biol. 108, 865-874]. Here, we show that this "acidosomal" fraction also contains a high-affinity vanadate-sensitive Ca2+ uptake activity that is stimulated by the pH gradient formed by the H(+)-ATPase. We attribute this Ca2+ uptake to the presence of a H(+)-countertransporting Ca(2+)-ATPase, pumping Ca2+ into an acidic compartment.

Acid-Base Equilibrium

Potential morphogens involved in pattern formation during Dictyostelium differentiation.

Upon starvation, Dictyostelium amoebae aggregate together and then differentiate into either the stalk or spore cells that, respectively, form the stalk and sorus of the fruiting body. During differentiation, the prestalk and prespore cells become spatially segregated in a clearly defined developmental pattern. Several low molecular weight molecules that influence cell type determination during in vitro differentiation have been identified. The possible role of these molecules as morphogens, responsible for the formation of the developmental pattern, is discussed.

Adenosine

Nested polymerase chain reaction assay for the detection of cytomegalovirus overcomes false positives caused by contamination with fragmented DNA.

The polymerase chain reaction (PCR) technique offers a promising alternative to tissue culture for the rapid and sensitive detection of cytomegalovirus (CMV) infection. However, high levels of background amplification detected in samples containing water but no DNA make interpretation of borderline positive samples extremely difficult and reduce the sensitivity of the assay. The signal from amplification of water or positive samples can be eliminated by DNase treatment, but not by filtration through anisotropic membrane, autoclaving, or ultraviolet irradiation. A lag time of 10 to 12 cycles is observed before the reactions with water will show product formation by liquid hybridization detection. The use of nested PCR eliminates the background and, in serial dilutions of a positive sample, shows a 500- to 1000-fold increase in sensitivity by liquid hybridization detection. We suggest that the background signal is arising from small fragments of DNA, which may be produced by autoclaving viral culture material. Such fragments would escape filtration, and overlapping fragments of DNA can prime one another to form complete mosaic sequences that will then amplify. Nested PCR, appropriately controlled for the number of cycles at each step, should successfully overcome such false positives caused by fragmented DNA, no matter if the contamination occurs at the collection site, in processing, or at the facility performing the test.

Base Sequence

The effect of ammonia on cell-type-specific enzyme accumulation in Dictyostelium discoideum.

We have shown that ammonia inhibits stalk cell formation and promotes spore formation during cyclic AMP induced differentiation of monolayers of sporogenous amoebae (Gross, J.D. et al., Nature (London), 303, 244-245, 1983). Here we show that exposure to ammonia favours the accumulation of prespore- over prestalk-specific enzymes and related products. We conclude that ammonia switches cells from the prestalk to the prespore pathway rather than simply inhibiting stalk cell maturation and hence may act as a morphogen during development.

Acid Phosphatase