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Diffusion as a ruler: Modeling kinesin diffusion as a length sensor for intraflagellar transport

Hendel, N. L. and Thomson, M. and Marshall, W. F. (2017) Diffusion as a ruler: Modeling kinesin diffusion as a length sensor for intraflagellar transport. Molecular Biology of the Cell, 28 (26). Art. No. M196. ISSN 1059-1524. https://resolver.caltech.edu/CaltechAUTHORS:20180321-144810107

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Abstract

An important question in cell biology is whether cells are able to measure size, either whole cell size or organelle size. Perhaps cells have an internal chemical representation of size that can be used to precisely regulate growth, or perhaps size is just an accident that emerges due to constraint of nutrients. The eukaryotic flagellum is an ideal model for studying size sensing and control because its linear geometry makes it essentially one‐dimensional, greatly simplifying mathematical modeling. The assembly of flagella is regulated by intraflagellar transport (IFT), in which kinesin motors carry cargo adaptors for flagellar proteins along the flagellum and then deposit them at the tip, lengthening the flagellum. The rate at which IFT motors are recruited to begin transport into the flagellum is anticorrelated with the flagellar length, implying some kind of communication between the base and the tip and possibly indicating that cells contain some mechanism for measuring flagellar length. Although it is possible to imagine many complex scenarios in which additional signaling molecules sense length and carry feedback signals to the cell body to control IFT, might the already‐known components of the IFT system be sufficient to allow length dependence of IFT? Here, we investigate a model in which the anterograde kinesin motors unbind after cargo delivery, diffuse back to the base, and are subsequently reused to power entry of new IFT trains into the flagellum. By modeling such a system at three different levels of abstraction we are able to show that the diffusion time of the motors can in principle be sufficient to serve as a proxy for length measurement. In all three implementations, we found that the diffusion model can not only achieve a stable steady‐state length without the addition of any other signaling molecules or pathways, but also is able to produce the anticorrelation between length and IFT recruitment rate that has been observed in quantitative imaging studies.


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URLURL TypeDescription
https://doi.org/10.1091/mbc.E17-10-0618DOIAbstracts
http://www.molbiolcell.org/content/28/26/3727PublisherAbstracts
http://resolver.caltech.edu/CaltechAUTHORS:20180212-080247041Related ItemArticle
Additional Information:© 2017 American Society for Cell Biology. Free via Creative Commons 2 months after publication.
Issue or Number:26
Record Number:CaltechAUTHORS:20180321-144810107
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20180321-144810107
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:85405
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:26 Mar 2018 21:34
Last Modified:03 Oct 2019 19:30

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