The recovery of normal DNA replication kinetics in ultraviolet-irradiated Chinese hamster cells

The kinetics of DNA replication were analyzed in the second S phase following UV irradiation of Chinese hamster ovary cells synchronized at the beginning of S phase. The cells were synchronized by treating cells selected in mitosis with hydroxyurea for 9 h. Following UV irradiation, the cells were allowed to progress until the next mitosis; at which time they were resynchronized at the beginning of the second S phase by the same procedure. The kinetics of DNA replication were determined by measuring the proportion of DNA which achieved hybrid buoyant density on CsCl density gradients as a function of the time of incubation in the presence of 5-bromodeoxyuridine.The results of these experiments showed that even though the rate of DNA replication is substantially depressed during the first S phase following UV irradiation with a fluence of 5 J/m², the rate has recovered to the extent that it is indistinguishable from the unirradiated control by the time the cells have entered their second S phase. It was concluded from these observations that the lesions in DNA which caused the rate of DNA replication to be initially depressed during the first S phase have been either removed or modified such that they no longer are able to cause a reduction in the rate of DNA replication in the second S phase following UV irradiation.     

Amino acid accumulation in frog muscle. II. Are cycloleucine fluxes consistent with an adsorption model for concentrative uptake of amino acid?

Cycloleucine accumulation by frog muscle was studied at o °C and 25 °C. At external concentrations less than 5 mM the distribution ratio of cycloleucine is higher at 0 °C than at 25 °C. At concentrations greater than 5 mM the converse is true due to apparent exclusion of cycloleucine from a larger portion of the cell water at 0 °C.The steady state data are consistent with an absortion model for amino acid accumulation. Flux studies provide a means to rule out this model if all the possible rate-limiting steps in the movement of amino acid into and out of the cell are considered. These steps include intra-cytoplasmic diffusion, desorption from cytoplasmic or membrane sites and passage through the cell membrane. The assumption is made that the rate-limiting step for influx and efflux is the same, allowing the use of either influx or efflux data to examine the model.Diffusion-limited flux is ruled out on the basis of“influx profile analysis” of the time course of cycloleucine entry at both 0 °C and 25 °C.At least 95% of all intracellular cycloleucine leaves frog muscle cells with a single exponential time course at both 0 °C. The rate constant of efflux does not vary with cellular concentration.These findings are shown to be incompatible with desorption-limited efflux. They are compatible with membrane-limited efflex only if (i) adsorption sites are located on membranes with direct access to the extracellular space and (ii) the rate constant for desorption is equal to the rate constant of membrane-limited efflux of free amino acid. It is considered unlikely that such a coincidence would occur at both 0 °C and 25 °C. Therefore, an absorption model for cycloleucine accumulation in frog muscle appears to be untenable.     

High Performance Liquid Chromatography-Based Reevaluation of Disaccharides Produced upon Incubation of Sugarcane Vacuoles with UDP-Glucose

A reanalysis of products formed after short-term incubation of sugarcane (Saccharum spp. hybrid cv H50-7209) vacuole preparations with uridine diphosphate [¹⁴C]glucose was performed. The results indicated that the ethanol-soluble substance previously identified as sucrose did not elute with sucrose when subjected to high performance liquid chromatography but had the same retention time as a disaccharide tentatively identified as laminaribiose.     

The localisation of an Mr 74,000 major chromatin antigen on native salivary chromosomes of Drosophila melanogaster

An antigen making a major contribution to the immune response to Drosophila melanogaster chromatin resides primarily on a nonhistone charge-class family of proteins of Mr 74,000. Immunofluorescence detects this antigen at interbands, puffs and diffuse bands of D. melanogaster salivary chromosomes isolated without exposure to acid fixatives, and on nucleoplasmic ribonucleoprotein droplets. In the electron microscope, gold labelling reveals the binding of monoclonal antibodies specific for the antigen at chromosomal loci generally bearing putative ribonucleoprotein (RNP) particles. However, the locus 3C 11–12 is remarkable in that it bears putative RNP particles but is virtually unlabelled, suggesting protein specificity at different active loci.     

PALEOZOIC LYCOPSID FRUCTIFICATIONS. I. LEPIDOCARPON PETRIFACTIONS

A reinvestigation of the 4 American species of Lepidocarpon described from petrifactions and of Illiniocarpon cadyi, also described from petrifactions, shows that they are all conspecific. When they, in turn, are compared with specimens of the British petrifaction L. lomaxi, no significant differences can be demonstrated. The criteria cited as diagnostic for the American petrifaction species of Lepidocarpon were found to fail as bases of discrimination when 400 specimens of Lepidocarpon found in coal balls of Pennsylvanian age were studied. Measurements and observations made of a sample size of 136 of these 400 specimens reveal a degree of variation compatible with that of a single species. All previously described American and British petrifaction taxa fall within (or not significantly beyond) this range of variability of a single species as determined from this sample. Additional evidence concerning the 3-dimensional sporophyll structure of this one species of Lepidocarpon and the configurations obtained by certain planes of section through it have served to demonstrate that Illiniocarpon cadyi is in reality a taxon based on sectioned structures of the sporophyll of this Lepidocarpon species. Under the rules of priority, this species of Lepidocarpon and the following are assigned to Lepidocarpon lomaxi: Illiniocarpon cadyi, Lepidocarpon ioense, L. magnificum (megasporangiate form), L. crenatum and L. palmerensis. On the basis of the morphological evidence, the British petrifaction described as Lepidocarpon wildianum is also equated with L. lomaxi.     

HYBRIDS AND GENOME RELATIONS OF HIBISCUS SABDARIFFA,H. MEEUSEI,H. RADIATUS AND H. ACETOSELLA

Chromosome pairing was studied in the following hybrids: Hibiscus radiatus-meeusei (tetraploid F₁), H. sabdariffa-meeusei (tetraploid F₁ and spontaneous allooctoploid F₂), and hexaploid H. acetosella-(sabdariffa-meeusei). Genome constitutions of the species adduced from these data are symbolized as follows: H. radiatus and H. acetosella, AABB; H. meeusei, AAXX; H.sabdariffa, XXYY or AAYY.