A Keller-Segel model for C elegans L1 aggregation.

We describe a mathematical model for the aggregation of starved first-stage C elegans larvae (L1s). We propose that starved L1s produce and respond chemotactically to two labile diffusible chemical signals, a short-range attractant and a longer range repellent. This model takes the mathematical form...

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Main Authors: Leon Avery, Brian Ingalls, Catherine Dumur, Alexander Artyukhin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-07-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1009231
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author Leon Avery
Brian Ingalls
Catherine Dumur
Alexander Artyukhin
author_facet Leon Avery
Brian Ingalls
Catherine Dumur
Alexander Artyukhin
author_sort Leon Avery
collection DOAJ
description We describe a mathematical model for the aggregation of starved first-stage C elegans larvae (L1s). We propose that starved L1s produce and respond chemotactically to two labile diffusible chemical signals, a short-range attractant and a longer range repellent. This model takes the mathematical form of three coupled partial differential equations, one that describes the movement of the worms and one for each of the chemical signals. Numerical solution of these equations produced a pattern of aggregates that resembled that of worm aggregates observed in experiments. We also describe the identification of a sensory receptor gene, srh-2, whose expression is induced under conditions that promote L1 aggregation. Worms whose srh-2 gene has been knocked out form irregularly shaped aggregates. Our model suggests this phenotype may be explained by the mutant worms slowing their movement more quickly than the wild type.
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spelling doaj.art-be9bf7ec68a94de1a31719aec04d19bf2022-12-21T23:37:58ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582021-07-01177e100923110.1371/journal.pcbi.1009231A Keller-Segel model for C elegans L1 aggregation.Leon AveryBrian IngallsCatherine DumurAlexander ArtyukhinWe describe a mathematical model for the aggregation of starved first-stage C elegans larvae (L1s). We propose that starved L1s produce and respond chemotactically to two labile diffusible chemical signals, a short-range attractant and a longer range repellent. This model takes the mathematical form of three coupled partial differential equations, one that describes the movement of the worms and one for each of the chemical signals. Numerical solution of these equations produced a pattern of aggregates that resembled that of worm aggregates observed in experiments. We also describe the identification of a sensory receptor gene, srh-2, whose expression is induced under conditions that promote L1 aggregation. Worms whose srh-2 gene has been knocked out form irregularly shaped aggregates. Our model suggests this phenotype may be explained by the mutant worms slowing their movement more quickly than the wild type.https://doi.org/10.1371/journal.pcbi.1009231
spellingShingle Leon Avery
Brian Ingalls
Catherine Dumur
Alexander Artyukhin
A Keller-Segel model for C elegans L1 aggregation.
PLoS Computational Biology
title A Keller-Segel model for C elegans L1 aggregation.
title_full A Keller-Segel model for C elegans L1 aggregation.
title_fullStr A Keller-Segel model for C elegans L1 aggregation.
title_full_unstemmed A Keller-Segel model for C elegans L1 aggregation.
title_short A Keller-Segel model for C elegans L1 aggregation.
title_sort keller segel model for c elegans l1 aggregation
url https://doi.org/10.1371/journal.pcbi.1009231
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