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Coagulation-fragmentation for a finite number of particles and application to telomere clustering in the yeast nucleus

Published 13 years agoVersion 1arXiv:1201.2620

Authors

Nathanael Hoze, David Holcman

Categories

q-bio.SCmath-ph

Abstract

We develop a coagulation-fragmentation model to study a system composed of a small number of stochastic objects moving in a confined domain, that can aggregate upon binding to form local clusters of arbitrary sizes. A cluster can also dissociate into two subclusters with a uniform probability. To study the statistics of clusters, we combine a Markov chain analysis with a partition number approach. Interestingly, we obtain explicit formulas for the size and the number of clusters in terms of hypergeometric functions. Finally, we apply our analysis to study the statistical physics of telomeres (ends of chromosomes) clustering in the yeast nucleus and show that the diffusion-coagulation-fragmentation process can predict the organization of telomeres.

Coagulation-fragmentation for a finite number of particles and application to telomere clustering in the yeast nucleus

13 years ago
v1
2 authors

Categories

q-bio.SCmath-ph

Abstract

We develop a coagulation-fragmentation model to study a system composed of a small number of stochastic objects moving in a confined domain, that can aggregate upon binding to form local clusters of arbitrary sizes. A cluster can also dissociate into two subclusters with a uniform probability. To study the statistics of clusters, we combine a Markov chain analysis with a partition number approach. Interestingly, we obtain explicit formulas for the size and the number of clusters in terms of hypergeometric functions. Finally, we apply our analysis to study the statistical physics of telomeres (ends of chromosomes) clustering in the yeast nucleus and show that the diffusion-coagulation-fragmentation process can predict the organization of telomeres.

Authors

Nathanael Hoze, David Holcman

arXiv ID: 1201.2620
Published Jan 12, 2012

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