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Stochastic effects in retrotransposon dynamics revealed by modeling under competition for cellular resources. / Pavlov, Sergey; Gursky, Vitaly V.; Samsonova, Maria; Kanapin, Alexander; Samsonova, Anastasia.

в: Life, Том 11, № 11, 1209, 01.11.2021.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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@article{e1f9bdefb7644785a3e57ee57d31fb4e,
title = "Stochastic effects in retrotransposon dynamics revealed by modeling under competition for cellular resources",
abstract = "Transposons are genomic elements that can relocate within a host genome using a {\textquoteleft}cut{\textquoteright}-or {\textquoteleft}copy-and-paste{\textquoteright} mechanism. They make up a significant part of many genomes, serve as a driving force for genome evolution, and are linked with Mendelian diseases and cancers. Interactions between two specific retrotransposon types, autonomous (e.g., LINE1/L1) and nonautonomous (e.g., Alu), may lead to fluctuations in the number of these transposons in the genome over multiple cell generations. We developed and examined a simple model of retrotransposon dynamics under conditions where transposon replication machinery competed for cellular resources: namely, free ribosomes and available energy (i.e., ATP molecules). Such competition is likely to occur in stress conditions that a malfunctioning cell may experience as a result of a malignant transformation. The modeling revealed that the number of actively replicating LINE1 and Alu elements in a cell decreases with the increasing competition for resources; however, stochastic effects interfere with this simple trend. We stochastically simulated the transposon dynamics in a cell population and showed that the population splits into pools with drastically different transposon behaviors. The early extinction of active Alu elements resulted in a larger number of LINE1 copies occurring in the first pool, as there was no competition between the two types of transposons in this pool. In the other pool, the competition process remained and the number of L1 copies was kept small. As the level of available resources reached a critical value, both types of dynamics demonstrated an increase in noise levels, and both the period and the amplitude of predator–prey oscillations rose in one of the cell pools. We hypothesized that the presented dynamical effects associated with the impact of the competition for cellular resources inflicted on the dynamics of retrotransposable elements could be used as a characteristic feature to assess a cell state, or to control the transposon activity.",
keywords = "Cellular resources, Gillespie algorithm, Mobile genetic elements, Predator–prey model, Retrotransposons, Stochastic dynamics",
author = "Sergey Pavlov and Gursky, {Vitaly V.} and Maria Samsonova and Alexander Kanapin and Anastasia Samsonova",
year = "2021",
month = nov,
day = "1",
doi = "10.3390/life11111209",
language = "русский",
volume = "11",
journal = "Life",
issn = "0024-3019",
publisher = "MDPI AG",
number = "11",

}

RIS

TY - JOUR

T1 - Stochastic effects in retrotransposon dynamics revealed by modeling under competition for cellular resources

AU - Pavlov, Sergey

AU - Gursky, Vitaly V.

AU - Samsonova, Maria

AU - Kanapin, Alexander

AU - Samsonova, Anastasia

PY - 2021/11/1

Y1 - 2021/11/1

N2 - Transposons are genomic elements that can relocate within a host genome using a ‘cut’-or ‘copy-and-paste’ mechanism. They make up a significant part of many genomes, serve as a driving force for genome evolution, and are linked with Mendelian diseases and cancers. Interactions between two specific retrotransposon types, autonomous (e.g., LINE1/L1) and nonautonomous (e.g., Alu), may lead to fluctuations in the number of these transposons in the genome over multiple cell generations. We developed and examined a simple model of retrotransposon dynamics under conditions where transposon replication machinery competed for cellular resources: namely, free ribosomes and available energy (i.e., ATP molecules). Such competition is likely to occur in stress conditions that a malfunctioning cell may experience as a result of a malignant transformation. The modeling revealed that the number of actively replicating LINE1 and Alu elements in a cell decreases with the increasing competition for resources; however, stochastic effects interfere with this simple trend. We stochastically simulated the transposon dynamics in a cell population and showed that the population splits into pools with drastically different transposon behaviors. The early extinction of active Alu elements resulted in a larger number of LINE1 copies occurring in the first pool, as there was no competition between the two types of transposons in this pool. In the other pool, the competition process remained and the number of L1 copies was kept small. As the level of available resources reached a critical value, both types of dynamics demonstrated an increase in noise levels, and both the period and the amplitude of predator–prey oscillations rose in one of the cell pools. We hypothesized that the presented dynamical effects associated with the impact of the competition for cellular resources inflicted on the dynamics of retrotransposable elements could be used as a characteristic feature to assess a cell state, or to control the transposon activity.

AB - Transposons are genomic elements that can relocate within a host genome using a ‘cut’-or ‘copy-and-paste’ mechanism. They make up a significant part of many genomes, serve as a driving force for genome evolution, and are linked with Mendelian diseases and cancers. Interactions between two specific retrotransposon types, autonomous (e.g., LINE1/L1) and nonautonomous (e.g., Alu), may lead to fluctuations in the number of these transposons in the genome over multiple cell generations. We developed and examined a simple model of retrotransposon dynamics under conditions where transposon replication machinery competed for cellular resources: namely, free ribosomes and available energy (i.e., ATP molecules). Such competition is likely to occur in stress conditions that a malfunctioning cell may experience as a result of a malignant transformation. The modeling revealed that the number of actively replicating LINE1 and Alu elements in a cell decreases with the increasing competition for resources; however, stochastic effects interfere with this simple trend. We stochastically simulated the transposon dynamics in a cell population and showed that the population splits into pools with drastically different transposon behaviors. The early extinction of active Alu elements resulted in a larger number of LINE1 copies occurring in the first pool, as there was no competition between the two types of transposons in this pool. In the other pool, the competition process remained and the number of L1 copies was kept small. As the level of available resources reached a critical value, both types of dynamics demonstrated an increase in noise levels, and both the period and the amplitude of predator–prey oscillations rose in one of the cell pools. We hypothesized that the presented dynamical effects associated with the impact of the competition for cellular resources inflicted on the dynamics of retrotransposable elements could be used as a characteristic feature to assess a cell state, or to control the transposon activity.

KW - Cellular resources

KW - Gillespie algorithm

KW - Mobile genetic elements

KW - Predator–prey model

KW - Retrotransposons

KW - Stochastic dynamics

UR - https://www.mendeley.com/catalogue/8e41f108-132f-3c42-a984-9887b1aa7041/

U2 - 10.3390/life11111209

DO - 10.3390/life11111209

M3 - статья

VL - 11

JO - Life

JF - Life

SN - 0024-3019

IS - 11

M1 - 1209

ER -

ID: 104088438