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V A Berdnikov

Publications and source records attributed to V A Berdnikov.

At least 19 recordsLinked to original sources

[Determination of lysine residue number, positive charge and molecular lengths of histone H1 and H5 by a method of incomplete succinylation].

A simple method for determination of lysine residue number and positive charge of histones H1 and H5 in the acetic acid -- urea system has been developed. The method is based on incomplete succinylation of lysine residues and allows an accurate determination of protein molecular length. The accuracy of the method has been demonstrated by determination of goose and chicken histones H5 and their fragments. The calibrating curve for determination of molecular lengths of histones H1 and H5 has been plotted. Using the incomplete succinylation method, a detailed analysis of Lymantria dispar histone H1 structure has been carried out. The method under discussion can be used for determining lysine residue number, positive charge and molecular length of practically any protein.

Acylation

[Histones of Salmonidae fishes. Comparative study of histones from different species and intraspecies variability of Oncorhynchus nerka H1].

The comparative electrophoretic properties of erythrocyte histones from 7 Salmonidae species were investigated. Using Na-SDS gel electrophoresis, it was shown that all the species studied possess the erythrocyte-specific fraction of histone H5. High resolution gel electrophoresis in acetic acid--urea gels demonstrated differences in the subfractional composition of histone H1 from erythrocytes and liver of O. nerka. The analysis of the sample of 40 individuals from the same population revealed the existence of intraspecies polymorphism in histone H1 subfractional composition.

Animals

[Study of evolutionary changes in subfraction composition of histone H1 in birds].

Analysis of electrophoretic mobility of histone H1 subfractions from liver, brain and erythrocytes of 41 bird species was carried out. Subfractions of erythrocyte H1 histones from each species were compared with those of thrush Turdus musicus. The majority of species proved to possess a set of electrophoretically similar subfractions. Interspecific differences in histone H1 were mainly due to the differences in the ratio of those subfractions. The identity of the electrophoretic mobility and similar contribution to H1 histone from the respective tissues in different species permits to consider certain subfractions as homologous ones. The conservation of electrophoretic mobility for homologous subfractions of the birds of different orders shows a high evolutionary conservatism of the corresponding genes. It seems that in the course of evolution only a change in the expression of some of those genes occurs.

Animals

[Microelectrophoretic analysis of histones from single chromosomes and nucleoli of mosquito (Chironomis plumosus) larvae].

A simple method of microelectrophoresis for histone analysis from single fragments of polythenic chromosomes of chironomid salivary glands has been developed. The chromosomes or their fragments obtained micrurgically were dissolved in a microdroplet of 8 M urea and 1 N sulfuric acid solution. Electrophoresis was performed in 30--60 m diameter polyacrylamide gel cylinders under a layer of vaseline oil. The histones were separated into 6 electrophoretic bands which correspond to fractions H4, H2b, H2a+H3, H3-dimer, and two subfractions of histone H1. Comparison of histone electrophoregrams of the I, II, and III chromosomes showed their almost absolute identity. The ratio of fractions H4, H3, H2A, H2B as well as the ratio of histone H1 subfractions in the nucleus and in the rest of the IV chromosome cannot be visually distinguished.

Cell Fractionation