High allozyme variation in populations of three spiny rat species from Upper Amazonia: association with ecology and evolution]

The allozyme variation in three spiny rat species of the genus Proechimys from Upper Amazonia was studied in relation to their ecology and evolution. The ecological environmental factors and biotopic distribution of species were analyzed. The unusually high allozyme variation was found in P. simonsi and P. sp. (2n = 34) inhabiting native forest biotopes. A relatively low allozyme variation in P. brevicauda was assumed to be associated with eurybiotic properties and the ability of this species to adapt to anthropogenic biotopes. Data on chromosome homeology and reconstruction of chromosome rearrangements in six spiny rat species were correlated with allozyme variation. The results suggested that chromosome rearrangements played the major role in evolution of the spiny rat species, and that the reorganization of the P. brevicauda genome was not random. P. simonsi and P. sp. (2n = 34), which live in native forest biotopes and carry an excessive genomik "informational load", were assumed to be highly susceptible to any novel external factors. These species are potentially able to produce new chromosome forms and are most significantly affected by deforestation.     

Masugi's nephritis: preparation of an active nephrotoxic serum

An active nephrotoxic serum (NTS) was prepared by immunization of rabbits with isolated renal glomeruli of rats and Freund's complete adjuvant. The glomeruli were isolated from the renal cortex by the sieving procedure. Intravenous injection of the NTS to rats induced the development of marked proteinuria and the nephrotic syndrome. Histological and electron microscopic studies of renal tissue performed by days 5 and 15 since the first injection of the NTS revealed extracapillary proliferative glomerulonephritis. IgG depositions on the basal membranes of the glomerular capillaries were linear on day 5 and granular on day 15 since the first injection of the NTS.     

A compact form of DNA in solution. III. Influence of the ion composition of the solution on the compactization process of double-stranded DNA in the presence of peg]

The data showing the features of the DNA compactization process in PEG-containing solutions of chlorides of different alkaline metals (LiCl, KCl, RbCl and CsCl) and an ammonium salt (CH3-(CH2)17-N-(CH3)3Br) are presented. The data indicate that the formation of a compact form of the double-stranded DNA in PEG-containing water-salt solutions depends not only on the PEG concentration and ionic strength but on tha cation nature as well. The compactization occurs most easily in the presence of Na+-ions. This indicates a specific character of interaction between Na+-ions and DNA phosphate groups which may be due to an optimum structural fit between the hydrated Na+-ions and orientation of the phosphate groups in the DNA molecule. The nature of forces involved in the processes of the intramolecular compactization and intermolecular aggregation of double-stranded DNA molecules in water-salt solution is discussed. The difference between the effect of Na+ and that of K+-ions on the compactization process at the ionic strengths close to physiological values makes it possible to suggest that the changes of the tertiary structure of double-stranded DNA which accompany its function in vivo may take place under conditions of a decreased water activity at the expense of relatively slight changes in ion composition of the water surrounding DNA.     

Compaction of 2-chain DNA as a method of procedure in determining its binding constant with antibiotics]

The binding of antibiotics and dyes with a compact form of DNA produced in water-salt solutions containing polyethylenglycol (PEG) presents a possibility of studying antibiotic interaction with DNA molecules contained in biological objects, such as viruses and chromosomes, since the compact form of DNA reflects some DNA properties in vivo. Possibly the use of the compact and not the "open" or linear form of DNA in chemical reactions will provide data on the efficiency of the compound "action" under conditions close to intracellular ones. The results well be useful in screening substances with "optimal" pharmacological effect. The paper presents a method for determination of the constant of antibiotic or dye binding with DNA and two-chain synthetic polynucleotides in water-salt solutions containing PEG. The method is based on "elimination" of the DNA molecules in the form of compact particles bound in a complex with an antibiotic or a dye. Comparison of the data with the results of estimation of the constants of antibiotic binding with DNA by the routine methods showed close conformity of the binding constants determined by different methods. It was found that the value of the binding constant of the antibiotics studied slightly depended on the structural state of DNA. The value was practically the same for the linear and the compact forms of DNA.     

Study of conformation characteristics of polydeoxyribonucleotides with non-random base sequence by slow 1H----3H exchange

The rate constants of 1H----3H exchange between water and C8H-groups of purinic residues of alternating polynucleotides: poly[d(A-T)].poly[d(A-T)] (I), poly[d(G-C)].poly[d(G-C)] (II), poly[d(A-C)].poly[d(G-T)] (III) and homopolynucleotides: poly(dA).poly(dt) (IV), poly(dG).poly(dC) (V), as well as DNA E. coli, was determined in 0.15 M NaCl at 25 degrees C. The retardation of exchange observed at these conditions (compared to that of the B-form DNA) is in agreement with the model of B-alternating structure for the (I) and is attributed to the co-existence of B- and A-conformers for the (V) in solution. Absence of distinguishable differences in exchange rate constants for purinic residues of the (II), (III) and (IV) (compared to that of the B-form DNA) evidences that conformations of these polynucleotides in solution are similar to "canonical" B-form DNA and don't correlate with the model of "heteronomous" DNA which was proposed for (IV).