The Effect of Vaccinium vitis-idaea on Properties of Mountain-Meadow Soil under Alpine Lichen Heath

Russian Journal of Ecology - Abstract—The study of the effect of mycorrhiza symbiosis on the transformation of carbon and nitrogen compounds in soils is important in view of the necessity to...     

Effect of illumination regime on life span in <Emphasis Type="Italic">Drosophila melanogaster</Emphasis>

Accelerated aging of Drosophila strains with impaired detoxification of free radicals (Sod) and DNA repair (mus-210) under illumination as compared to the wild type has been demonstrated. In contrast, in a strain carrying a defective homolog of mammalian gene PCNA, the life span increases under conditions of round-the-clock illumination compared to constant darkness. The first review of the possible mechanisms underlying the effect of the illumination regime on the life span is presented, with special emphasis on the roles of the disturbance of normal circadian rhythms, increase in fecundity and physical activity (metabolic rate), and the neuroendocrine control of the insulin/IGF-1 pathway.     

Quantitative reconstruction of peatland hydrological regime with fossil testate amoebae communities

The effect of bog water table on the species structure of sphagnobiontic testate amoebae communities has been studied in peatland ecosystems of European Russia. On this basis, a transfer function (model) for quantitative paleoreconstructions has been developed. This involved the formation of a training dataset, construction of models, and testing their performance. As a result, the model constructed by weighted averaging regression has been adopted as optimal.     

Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia

Of 126 families referred for counselling of Duchenne muscular dystrophy (DMD), DNA analysis has been suggested to 119 families with at least one affected child or with an affected close male relative of the woman at risk of being a DMD carrier. A large proportion (about 80 per cent) of the families were represented by sporadic cases (only one affected individual). By means of multiplex polymerase chain reactions with different sets of oligoprimers providing amplification of 10–11 different exons, altogether 49 dystrophin gene deletions were identified (41 per cent). Eighteen deletions clustered in the 5′ ‘hot spot’ region of DMD cDNA and 36 in the distal half of the central rod domain around exons 43–53. An unusually high frequency (18 per cent) of deletions involving exons 17–19 was discovered. Large deletions extending through both ‘hot spot’ regions and thus occupying over 30–40 exons were recorded in five cases (10 per cent). Seventy-six of 94 families were found to be informative by RFLP analysis for intragenic or extragenetic DNA probes. Carrier status was ascertained in 20 and rejected in 32 female relatives in 40 DMD families. Eight DMD-affected fetuses were diagnosed prenatally by direct deletion testing or by RFLP analysis. Feasible interpopulation variations in the dystrophin gene deletion pattern are discussed. The prospects for more effective prenatal diagnosis and carrier detection in high-risk DMD families in Russia are briefly outlined.