A structured model and likelihood approach to estimate yeast prion propagon replication rates and their asymmetric transmission
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Department of Mathematics, University of ArizonaIssue Date
2022
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Santiago, F., & Sindi, S. (2022). A structured model and likelihood approach to estimate yeast prion propagon replication rates and their asymmetric transmission. PLoS Computational Biology, 18(7).Journal
PLoS Computational BiologyRights
Copyright © 2022 Santiago, Sindi. This is an open access article distributed under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Prion proteins cause a variety of fatal neurodegenerative diseases in mammals but are generally harmless to Baker’s yeast (Saccharomyces cerevisiae). This makes yeast an ideal model organism for investigating the protein dynamics associated with these diseases. The rate of disease onset is related to both the replication and transmission kinetics of propagons, the transmissible agents of prion diseases. Determining the kinetic parameters of propagon replication in yeast is complicated because the number of propagons in an individual cell depends on the intracellular replication dynamics and the asymmetric division of yeast cells within a growing yeast cell colony. We present a structured population model describing the distribution and replication of prion propagons in an actively dividing population of yeast cells. We then develop a likelihood approach for estimating the propagon replication rate and their transmission bias during cell division. We first demonstrate our ability to correctly recover known kinetic parameters from simulated data, then we apply our likelihood approach to estimate the kinetic parameters for six yeast prion variants using propagon recovery data. We find that, under our modeling framework, all variants are best described by a model with an asymmetric transmission bias. This demonstrates the strength of our framework over previous formulations assuming equal partitioning of intracellular constituents during cell division. © 2022 Santiago, Sindi. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.Note
Open access journalISSN
1553-734XPubMed ID
35776712Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1371/journal.pcbi.1010107
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Except where otherwise noted, this item's license is described as Copyright © 2022 Santiago, Sindi. This is an open access article distributed under the terms of the Creative Commons Attribution License.
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