DNA repair mechanisms in dividing and non-dividing cells

DNA damage created by endogenous or exogenous genotoxic agents can exist in multiple forms, and if allowed to persist, can promote genome instability and directly lead to various human diseases, particularly cancer, neurological abnormalities, immunodeficiency and premature aging. To avoid such deleterious outcomes, cells have evolved an array of DNA repair pathways, which carry out what is typically a multiple-step process to resolve specific DNA lesions and maintain genome integrity. To fully appreciate the biological contributions of the different DNA repair systems, one must keep in mind the cellular context within which they operate. For example, the human body is composed of non-dividing and dividing cell types, including, in the brain, neurons and glial cells. We describe herein the molecular mechanisms of the different DNA repair pathways, and review their roles in non-dividing and dividing cells, with an eye toward how these pathways may regulate the development of neurological disease.     

Longevity determined by developmental arrest genes in Caenorhabditis elegans

The antagonistic pleiotropy theory of aging proposes that aging takes place because natural selection favors genes that confer benefit early on life at the cost of deterioration later in life. This theory predicts that genes that impact development would play a key role in shaping adult lifespan. To better understand the link between development and adult lifespan, we examined the genes previously known to be essential for development. From a pool of 57 genes that cause developmental arrest after inhibition using RNA interference, we have identified 24 genes that extend lifespan in Caenorhabditis elegans when inactivated during adulthood. Many of these genes are involved in regulation of mRNA translation and mitochondrial functions. Genetic epistasis experiments indicate that the mechanisms of lifespan extension by inactivating the identified genes may be different from those of the insulin/insulin-like growth factor 1 (IGF-1) and dietary restriction pathways. Inhibition of many of these genes also results in increased stress resistance and decreased fecundity, suggesting that they may mediate the trade-offs between somatic maintenance and reproduction. We have isolated novel lifespan-extension genes, which may help understand the intrinsic link between organism development and adult lifespan.     

Embryogenic cells in plant tissue cultures: Occurrence and behavior

Summary Plants develop from meristems where cells proliferate and are partitioned into layers that eventually differentiate to form the various tissues and organs of the plant. A phenomenon unique to certain plant tissues is the ability to inducede nova a range of developmental patterns, including embryogenesis. The temporal and spacial distribution of these developmental competencies suggests that regulatory proteins, rather than a lack of signals or signal receptors, shield specific developmental genes from signals that otherwise would confuse development. Studies involving embryogenic cells demonstrate that they are not strongly shielded from developmental signals, thus they are not determined. Furthermore, the normal development of zygotic and somatic embryos is readily perturbed by abnormal physicochemical environments. This suggests that embryogeny remains developmentally plastic until differentiation is largely completed. The ability to induce somatic embryogenesis from specific tissues by specific signals is providing opportunities to further the molecular characterization of the menagerie of genetic regulation involved in development. Much of this review was presented at a Moet-Hennessy Louis Vuitton sponsored conference, Control of Morphogenesis in Plants, Aix Les Bains, France, September, 1989. Studies in our laboratory were supported in part by grants from the National Aeronautics and Space Administration (Cooperative Agreement No. NCC2-139), the Utah State University Biotechnology Center, and by the Utah Agricultural Experiment Station, Utah State University, Logan, UT 84322-4845 (approved as journal paper no. 3928).     

Faecal avoidance and the risk of infection by nematodes in a natural population of reindeer

We tested whether Svalbard reindeer (Rangifer tarandus platyrhynchus) minimise the risk of gastro- intestinal nematode infection by avoiding patches with a high density of faeces. This experiment was performed in preferred summer foraging habitat. The possibility that reindeer assess infection risk on the basis of faecal contamination levels across plant communities was determined by measuring the distribution of faeces in seven plant communities, and nematode developmental success in two plant communities with contrasting soil moisture content. We explored whether variation within individual reindeer in the levels of infection by gastro-intestinal nematodes was related to their diet. Reindeer avoided pastures where faecal contamination was increased, and thereby potentially reduced the risk of becoming infected by Trichostrongyle nematodes. Dung density was inversely related to soil moisture content, with high densities of faeces in dry plant communities and low densities in wet communities. However, nematode developmental success was positively related to soil moisture content, and was highest in the wetter sites. Thus, by avoiding dry areas with high dropping densities, reindeer would tend to feed in wetter areas where nematodes thrive. Therefore, dung density may be an unreliable predictor of the risk of infection. The absence of a strong relationship between an individual’s infection level and its diet might be due to the unpredictability of pasture infection level. Received: 8 July 1999 / Accepted: 20 January 2000