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Quantitative Analysis of Neuronal Dendritic Arborization Complexity in Drosophila
Published on: January 7, 2019
The rodent Four-jointed ortholog Fjx1 regulates dendrite extension
Barbara Probst1, Rebecca Rock, Manfred Gessler
1Abteilung Molekularbiologie, Institut für Allgemeine Zoologie und Genetik, Westfälische Wilhelms-Universität Münster, D-48149 Münster, Germany.
Abstract:
The extrinsic and intrinsic factors that regulate the size and complexity of dendritic arborizations are still poorly understood. Here we identify Fjx1, the rodent ortholog of the Drosophila planar cell polarity (PCP) protein Four-jointed (Fj), as a new inhibitory factor that regulates dendrite extension. The Drosophila gene four-jointed (fj) has been suggested to provide directional information in wing discs, but the mechanism how it acts is only poorly understood and the function of its mammalian homolog Fjx1 remains to be investigated. We analyzed the phenotype of a null mutation for mouse Fjx1. Homozygous Fjx1 mutants show an abnormal morphology of dendritic arbors in the hippocampus. In cultured hippocampal neurons from Fjx1 mutant mice, loss of Fjx1 resulted in an increase in dendrite extension and branching. Addition of Fjx1 to cultures of dissociated hippocampal neurons had the opposite effect and reduced the length of dendrites and decreased dendritic branching. Rescue experiments with cultured neurons showed that Fjx1 can act both cell-autonomously and non-autonomously. Our results identify Fjx1 as a new inhibitory factor that regulates dendrite extension.
Insights
Fjx1, a mammalian gene, acts as an inhibitory factor regulating neuron dendrite growth. Loss of Fjx1 leads to increased dendrite extension and branching in hippocampal neurons.
Area of Science:
- Neuroscience
- Developmental Biology
- Genetics
Background:
- Factors regulating dendritic arbor size and complexity are not fully understood.
- The function of Fjx1, the mammalian homolog of Drosophila Four-jointed (Fj), is largely unknown.
- Drosophila Fj is implicated in planar cell polarity (PCP) pathway signaling.
Purpose of the Study:
- To investigate the role of Fjx1 in regulating neuronal morphology.
- To identify Fjx1 as a potential factor controlling dendrite extension and branching.
Main Methods:
- Analysis of Fjx1 null mutant mice.
- Phenotypic analysis of dendritic arbors in hippocampal neurons from mutant mice.
- In vitro studies using cultured hippocampal neurons to assess Fjx1 function.
Main Results:
- Fjx1 null mutants exhibit abnormal dendritic arbor morphology in the hippocampus.
- Loss of Fjx1 in cultured neurons increases dendrite extension and branching.
- Exogenous Fjx1 application reduces dendrite length and branching.
- Fjx1 acts in both cell-autonomous and non-autonomous manners.
Conclusions:
- Fjx1 is identified as a novel inhibitory factor regulating dendrite extension.
- Fjx1 plays a significant role in controlling neuronal structure and complexity.
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