LIN-44/Wnt Directs Dendrite Outgrowth through LIN-17/Frizzled in C. elegans Neurons
2011

Wnt and Frizzled Proteins Regulate Dendrite Development in C. elegans Neurons

Sample size: 100 publication 10 minutes Evidence: high

Author Information

Author(s): Kirszenblat Leonie, Pattabiraman Divya, Hilliard Massimo A.

Primary Institution: Queensland Brain Institute, The University of Queensland, Brisbane, Australia

Hypothesis

Does the Wnt ligand LIN-44 and its Frizzled receptor LIN-17 regulate dendrite development in C. elegans neurons?

Conclusion

The study reveals that Wnt and Frizzled proteins play a crucial role in regulating dendrite outgrowth in C. elegans neurons.

Supporting Evidence

  • LIN-44 acts as an attractive cue for dendrite outgrowth.
  • Mutations in LIN-44 and LIN-17 lead to severe defects in dendrite formation.
  • Transgenic expression of LIN-44 can rescue dendrite defects in mutants.

Takeaway

This study shows that certain proteins help neurons grow their branches, which are important for sending and receiving signals.

Methodology

The researchers used genetic mutants and transgenic lines to analyze dendrite development in C. elegans.

Limitations

The study primarily focuses on a single type of neuron in C. elegans, which may limit the generalizability of the findings.

Participant Demographics

C. elegans nematodes were used as the model organism.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pbio.1001157

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