A mutual support mechanism through intercellular movement of CAPRICE and GLABRA3 can pattern the Arabidopsis root epidermis

The patterning of the Arabidopsis root epidermis depends on a genetic regulatory network that operates both within and between cells. Genetic studies have identified a number of key components of this network, but a clear picture of the functional logic of the network is lacking. Here, we integrate...

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Veröffentlicht in:PLoS biology 2008-09, Vol.6 (9), p.e235-e235
Hauptverfasser: Savage, Natasha Saint, Walker, Tom, Wieckowski, Yana, Schiefelbein, John, Dolan, Liam, Monk, Nicholas A M
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creator Savage, Natasha Saint
Walker, Tom
Wieckowski, Yana
Schiefelbein, John
Dolan, Liam
Monk, Nicholas A M
description The patterning of the Arabidopsis root epidermis depends on a genetic regulatory network that operates both within and between cells. Genetic studies have identified a number of key components of this network, but a clear picture of the functional logic of the network is lacking. Here, we integrate existing genetic and biochemical data in a mathematical model that allows us to explore both the sufficiency of known network interactions and the extent to which additional assumptions about the model can account for wild-type and mutant data. Our model shows that an existing hypothesis concerning the autoregulation of WEREWOLF does not account fully for the expression patterns of components of the network. We confirm the lack of WEREWOLF autoregulation experimentally in transgenic plants. Rather, our modelling suggests that patterning depends on the movement of the CAPRICE and GLABRA3 transcriptional regulators between epidermal cells. Our combined modelling and experimental studies show that WEREWOLF autoregulation does not contribute to the initial patterning of epidermal cell fates in the Arabidopsis seedling root. In contrast to a patterning mechanism relying on local activation, we propose a mechanism based on lateral inhibition with feedback. The active intercellular movements of proteins that are central to our model underlie a mechanism for pattern formation in planar groups of cells that is centred on the mutual support of two cell fates rather than on local activation and lateral inhibition.
doi_str_mv 10.1371/journal.pbio.0060235
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Genetic studies have identified a number of key components of this network, but a clear picture of the functional logic of the network is lacking. Here, we integrate existing genetic and biochemical data in a mathematical model that allows us to explore both the sufficiency of known network interactions and the extent to which additional assumptions about the model can account for wild-type and mutant data. Our model shows that an existing hypothesis concerning the autoregulation of WEREWOLF does not account fully for the expression patterns of components of the network. We confirm the lack of WEREWOLF autoregulation experimentally in transgenic plants. Rather, our modelling suggests that patterning depends on the movement of the CAPRICE and GLABRA3 transcriptional regulators between epidermal cells. Our combined modelling and experimental studies show that WEREWOLF autoregulation does not contribute to the initial patterning of epidermal cell fates in the Arabidopsis seedling root. 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subjects Arabidopsis
Arabidopsis - anatomy & histology
Arabidopsis - genetics
Arabidopsis - physiology
Arabidopsis Proteins - genetics
Arabidopsis Proteins - metabolism
Basic Helix-Loop-Helix Transcription Factors - genetics
Basic Helix-Loop-Helix Transcription Factors - metabolism
Cell Lineage
Computational Biology
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
Gene Expression Regulation, Developmental
Gene Expression Regulation, Plant
Gene Regulatory Networks
Hypotheses
Kinases
Mathematical models
Mathematics
Models, Biological
Morphogenesis - physiology
Plant Biology
Plant Epidermis - anatomy & histology
Plant Epidermis - physiology
Plant Roots - cytology
Plant Roots - metabolism
Plants, Genetically Modified - cytology
Plants, Genetically Modified - genetics
Plants, Genetically Modified - metabolism
Proteins
Proto-Oncogene Proteins c-myb - genetics
Proto-Oncogene Proteins c-myb - metabolism
Recombinant Fusion Proteins - genetics
Recombinant Fusion Proteins - metabolism
Transcription, Genetic
title A mutual support mechanism through intercellular movement of CAPRICE and GLABRA3 can pattern the Arabidopsis root epidermis
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