Dealing with DNA lesions: When one cell cycle is not enough

Subversion of genome integrity fuels cellular adaptation and is a prerequisite for organismal evolution, yet genomic lesions are also the harmful driving force of cancer and other age-related human diseases. Genome integrity maintenance is inherently linked to genome organization and nuclear architecture, which are substantially remodeled during the cell cycle. Here we discuss recent findings on how actively dividing cells cope with endogenous genomic lesions that occur frequently at repetitive, heterochromatic, and late replicating regions as byproducts of genome duplication. We discuss how such lesions, rather than being resolved immediately when they occur, are dealt with in subsequent cell cycle phases, and even after mitotic cell division, and how this in turn affects genome organization, stability, and function.     

Thermal response and reversibility of diapause in the eggs of Locusta migratoria

Abstract. Eggs of a local population of Locusta migratoria L. (Orthoptera: Acrididae) collected near Hirosaki (40.5^oN) entered diapause when incubated at temperatures between 20 and 35^oC. For diapause development the optimum temperature was 10^oC. The lower thermal threshold for post-diapause development was 14.7^oC. After chilling at 10^oC for 20 days, the rate of hatching varied with incubation temperature, being 0, 61% and 81% at 20, 25 and 30^oC, respectively. After chilling for 40 days or more, however, almost all eggs hatched at 20–30^oC. Diapause with a reduced intensity seemed to be eliminated easily by a high temperature of 25 or 30^oC.
When eggs chilled at 10^oC for 20 days were kept at 20^oC for 7 days or more before incubation at 25^oC, almost all eggs maintained diapause. Most eggs chilled at 10^oC for three 10 day periods separated by 3 days of warming at 25^oC failed to terminate diapause. Daily alternations of 10^oC (18 h) and 25^oC (6h) decreased the diapause-terminating effect of chilling. These facts suggest that diapause intensity can be restored if eggs chilled insufficiently are exposed to a moderately high temperature. This reversible change in diapause intensity would play an important role in maintaining diapause before winter.     

Vegetative multiplication and patch colonisation of Asarum europaeum subsp. europaeum L. (Aristolochiaceae) inferred by a combined morphological and molecular study

Asarum europaeum subsp. europaeum (Aristolochiaceae) is a rhizomatous herb forming distinct patches in calcareous broadleaved forests. Within natural stands, patches were mapped. In two regions, at least four patches were dug out, and connections between leaf modules through rhizomatous spacers were checked for signs of clonal reproduction (decay, breaking). Modules were sampled for amplified fragment length polymorphism (AFLP) fingerprinting to test whether they represent unique genets or are merigenets of a larger genet (split up by clonal reproduction), respectively.Morphologically, merigenet-relationships were only revealed in few cases with disrupted spacers between modules. With the obtained AFLP profiles for two primer combinations, the samples could be assigned to genets; clonal descendants of the same genet were readily identified. In one patch analysed in detail, 18 samples from 17 unconnected “plants” belonged to only two genets, which were morphologically divided into two and 15 merigenets, respectively. These two genets probably belonged to different maternal lineages and came into contact after lateral spread from the established clones. They showed divergent affinities to samples from adjacent patches (which all represented unique genets).The findings support the suitability of the combined morpho-ecological and molecular approach: compared to either method alone, it allows a more detailed analysis and interpretation of the fine-scale clonal structure, patch colonisation and especially of vegetative multiplication (with morpho-ecological studies to discern clonal growth and clonal reproduction and AFLP fingerprinting for genet and merigenet identification, respectively).     

Studies on maintenance of vector pBK2 in Corynebacterium acetoacidophilum by co-culture experiments in a continuous bioreactor

A plasmid vector pBK2 was tested for maintenance in Corynebacterium acetoacidophilum and found to be 100% stable for 90 generations. In co-culture experiments in absence of any selection pressure it was able to cause washout of plasmid free cells. Deletion mutagenesis of the plasmid was done to identify the regions of DNA responsible for its stable maintenance. This led to the identification of a region of DNA in pBB1, an endogenous plasmid used in the construction of pBK2, which is responsible for providing a growth rate advantage to the plasmid containing cell in co-culture with plasmid-free cells. To explain this observed stability we postulate the production of a “growth-inhibiting factor” by the plasmid-containing cells. Inclusion of a death rate term for the plasmid free cells in the computer simulation of the growth kinetics in a chemostat successfully predicts, depending upon the magnitude of the kinetic parameters, a stable coexistence of the two or washout of the plasmid-free cells, an observation that matches the experimental data. Because of its stable maintenance and its ability to select against plasmid-free cells this host-vector system is a natural candidate for cloning and use in large-scale fermentations.     

Studies on Trypanosoma vivax: Infectivity and serial maintenance of natural bovine isolates in mice

Studies were carried out on the ability of T. vivax to infect laboratory mice and on its subsequent maintenance between mice. On 38 out of 75 occasions, inoculation of mice with bovine T. vivax resulted in infection; in 3 instances, bovine blood, negative by other diagnostic tests, infected mice. Ten out of 21 bovine isolates could be subpassaged in mice for only a limited number of passages. Three additional isolates infective to mice, were maintainable serially between mice for an indefinite time. It appeared that only early natural infections were capable of infecting mice, each individual isolate surviving in the mice for a characteristic period. Those bovine isolates with the inherent property of serial maintenance between mice, did not change in their pathogenicity for ruminants.