Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs

Telomeres are guanine-rich sequences at the end of chromosomes which shorten during each replication event and trigger cell cycle arrest and/or controlled death (apoptosis) when reaching a threshold length. The enzyme telomerase replenishes the ends of telomeres and thus prolongs the life span of ce...

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Main Authors: Hirt, Bartholomäus V., Wattis, Jonathan A.D., Preston, Simon P.
Format: Article
Published: Springer 2014
Online Access:https://eprints.nottingham.ac.uk/3036/
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author Hirt, Bartholomäus V.
Wattis, Jonathan A.D.
Preston, Simon P.
author_facet Hirt, Bartholomäus V.
Wattis, Jonathan A.D.
Preston, Simon P.
author_sort Hirt, Bartholomäus V.
building Nottingham Research Data Repository
collection Online Access
description Telomeres are guanine-rich sequences at the end of chromosomes which shorten during each replication event and trigger cell cycle arrest and/or controlled death (apoptosis) when reaching a threshold length. The enzyme telomerase replenishes the ends of telomeres and thus prolongs the life span of cells, but also causes cellular immortalisation in human cancer. G-quadruplex (G4) stabilising drugs are a potential anticancer treatment which work by changing the molecular structure of telomeres to inhibit the activity of telomerase. We investigate the dynamics of telomere length in different conformational states, namely t-loops, G-quadruplex structures and those being elongated by telomerase. By formulating deterministic differential equation models we study the effects of various levels of both telomerase and concentrations of a G4-stabilising drug on the distribution of telomere lengths, and analyse how these effects evolve over large numbers of cell generations. As well as calculating numerical solutions, we use quasicontinuum methods to approximate the behaviour of the system over time, and predict the shape of the telomere length distribution. We find those telomerase and G4-concentrations where telomere length maintenance is successfully regulated. Excessively high levels of telomerase lead to continuous telomere lengthening, whereas large concentrations of the drug lead to progressive telomere erosion. Furthermore, our models predict a positively skewed distribution of telomere lengths, that is, telomeres accumulate over lengths shorter than the mean telomere length at equilibrium. Our model results for telomere length distributions of telomerase-positive cells in drug-free assays are in good agreement with the limited amount of experimental data available.
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spelling nottingham-30362020-05-04T20:14:33Z https://eprints.nottingham.ac.uk/3036/ Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs Hirt, Bartholomäus V. Wattis, Jonathan A.D. Preston, Simon P. Telomeres are guanine-rich sequences at the end of chromosomes which shorten during each replication event and trigger cell cycle arrest and/or controlled death (apoptosis) when reaching a threshold length. The enzyme telomerase replenishes the ends of telomeres and thus prolongs the life span of cells, but also causes cellular immortalisation in human cancer. G-quadruplex (G4) stabilising drugs are a potential anticancer treatment which work by changing the molecular structure of telomeres to inhibit the activity of telomerase. We investigate the dynamics of telomere length in different conformational states, namely t-loops, G-quadruplex structures and those being elongated by telomerase. By formulating deterministic differential equation models we study the effects of various levels of both telomerase and concentrations of a G4-stabilising drug on the distribution of telomere lengths, and analyse how these effects evolve over large numbers of cell generations. As well as calculating numerical solutions, we use quasicontinuum methods to approximate the behaviour of the system over time, and predict the shape of the telomere length distribution. We find those telomerase and G4-concentrations where telomere length maintenance is successfully regulated. Excessively high levels of telomerase lead to continuous telomere lengthening, whereas large concentrations of the drug lead to progressive telomere erosion. Furthermore, our models predict a positively skewed distribution of telomere lengths, that is, telomeres accumulate over lengths shorter than the mean telomere length at equilibrium. Our model results for telomere length distributions of telomerase-positive cells in drug-free assays are in good agreement with the limited amount of experimental data available. Springer 2014-05 Article PeerReviewed Hirt, Bartholomäus V., Wattis, Jonathan A.D. and Preston, Simon P. (2014) Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs. Journal of Mathematical Biology, 68 (6). pp. 1521-1552. ISSN 0303-6812 http://link.springer.com/article/10.1007%2Fs00285-013-0678-2 doi:10.1007/s00285-013-0678-2 doi:10.1007/s00285-013-0678-2
spellingShingle Hirt, Bartholomäus V.
Wattis, Jonathan A.D.
Preston, Simon P.
Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs
title Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs
title_full Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs
title_fullStr Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs
title_full_unstemmed Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs
title_short Modelling the regulation of telomere length: the effects of telomerase and G-quadruplex stabilising drugs
title_sort modelling the regulation of telomere length: the effects of telomerase and g-quadruplex stabilising drugs
url https://eprints.nottingham.ac.uk/3036/
https://eprints.nottingham.ac.uk/3036/
https://eprints.nottingham.ac.uk/3036/