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Iu A Eĭdel'man

Publications and source records attributed to Iu A Eĭdel'man.

4 recordsLinked to original sources

[Globular model of interphase chromosome and intrachromosomal exchange aberrations].

A globular folding model formerly proposed for large-scale interphase chromatin/chromosome organization is investigated here by computer simulation. Large-scale structure of interphase chromosome is suggested to be determined by volumetric interactions between chromosome subunits resulting in folding of subunit chain in a globular state. Structure unit of interphase chromosome is considered as a spherical structure consisting of a cluster of compact chromatin domains. These structure units/domain clusters were termed as a superdomains to emphasize their supradomain organization. Globular state of superdomain chain with excluded volume as well as phase transitions between condensed (globular) and decondensed (coiled) states are studied by dynamic Monte-Carlo approach. Globular model is supported by confocal microscopy data. It extends current view on interphase chromosome as a random Gauss polymer chain. Radiation-induced intrachromosome exchange aberrations (intrachanges) are modeled on the basis of the contact hypothesis. It implies that intrachanges result from radiation damage of chromatin mainly in contacted subunits. Computer modeling of chromosome structure provides a wealth of information about proximity effects and results in prediction of pattern of intrachromosome contacts. Calculated intrachange frequencies agree well with experimental data. Globular model suggests a physical mechanism for conformational changes of large-scale chromosome structure similar to phase transitions in polymer systems. These rearrangements of structure organization of chromosomes in the nuclei following irradiation could be mechanistically linked to the complex chromosome aberrations formation as well as to alteration of gene expression due to position variegation effect.

Chromatin↗

[Rejoining pathways underlying intrachange formation depend on interphase chromosome structure].

Fluorescence in situ hybridization technique with dual-arm painting of the same chromosome allows to study radiation induced intrachromosomal exchange aberrations (intrachanges). The formal method for analysis of FISH data developed by Savage and Simpson includes an arrangement of chromosomal reactive breaks on chromosomes and chromosome arms (CAB system). That method predicts types and frequencies of aberrations assuming random restitution/rejoining of breaks free ends. However experimental data suggest that many aberrations are formed non-uniformly along the chromosomes and chromosome arms. In the present paper the system for classifying rejoining pathways underlying intrachange formation is proposed which does not require random restitution/rejoining suggestion. It takes into account the parameters of interphase chromosome structure. Types and frequencies of intrachanges are considered by exploring different hypotheses about exchange initiating chromosomal lesions.

Chromosome Aberrations↗

[Biophysical modeling of radiation induced genetic damage to cells].

The paper deals with the new approach for high accurate prediction of ionising radiation induced lesions of the cellular genetic structures. The previous techniques mainly were based on the assumption of the random radiation-induced breakage of the cellular DNA. They did not consider higher-order DNA organisation in the chromatin and in the interphase chromosomes. The paper discusses the new methods of the biophysical modelling of DNA breakage following high LET irradiation which takes into account the information on 3-dimensional structural organisation of DNA in interphase chromosomes. On this basis the influence of DNA organisation in the chromosomes on both dsb clusters induction and on repair were quantitatively studied, that was impossible by the means of previous computational techniques.

Biophysical Phenomena↗

[Structural chromosome organisation and radiation-induced interchromosomal aberrations].

The quantitative prediction of the biological effects of radiation is one of the actual tasks of radiobiology. The experimental study may be impossible under certain conditions (low doses, complex radiation fields, etc). The development of theoretical tools is required to predict biological and medical consequence of the irradiation of cell and organism. The effect under the consideration in the present paper is chromosome aberrations (CA) induced by low and high LET radiation. One of the most uncertain factors in CA prediction is the impact of chromosomal and nuclear architecture. In the present study the quantitative evaluation of the mechanisms of CA induction are discussed in the framework of the biophysical modelling technique taking into account interphase chromosomes structure in the nucleus of living (human) cell. We show that the surface contacts mechanism of interchromosomal aberrations (interchange) formation does not explain the observed ratio of simple/complex interchanges induced by both low and high LET radiation. The chromatin structure repositioning following irradiation is proposed as a possible mechanism involved in the formation of the complex aberrations.

Cell Nucleus↗